Rebecca Buckley | Academic Influence

Rebecca Buckley's AcademicInfluence.com Rankings

Rebecca Buckley

Law

#1981

World Rank

#2464

Historical Rank

#936

USA Rank

Common Law

#63

World Rank

#70

Historical Rank

#14

USA Rank

International Law

#324

World Rank

#423

Historical Rank

#141

USA Rank

Rebecca Buckley

Biology

#4238

World Rank

#6353

Historical Rank

#1617

USA Rank

Immunology

#275

World Rank

#286

Historical Rank

#67

USA Rank

biology Degrees

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Rebecca Buckley's Degrees

Bachelors Biology University of California, Berkeley
Doctorate Pediatrics Stanford University

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Why Is Rebecca Buckley Influential?

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According to Wikipedia, Rebecca Hatcher Buckley is a medical doctor who has conducted research in pediatric immunological diseases. Biography Buckley graduated from Duke University in 1954 with a bachelor's degree. She received her Doctor of Medicine in 1958 from North Carolina School of Medicine, and training in pediatrics at Duke.

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Rebecca Buckley's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Chronic Granulomatous Disease: Report on a National Registry of 368 Patients (2000) (1583)
Gene therapy for immunodeficiency due to adenosine deaminase deficiency. (2009) (926)
Defective IL7R expression in T-B+NK + severe combined immunodeficiency (1998) (843)
Mutation of Jak3 in a Patient with SCID: Essential Role of Jak3 in Lymphoid Development (1995) (808)
Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency. (1999) (666)
Actionable diagnosis of neuroleptospirosis by next-generation sequencing. (2014) (665)
A randomized double-blind trial (2003) (663)
Use of intravenous immunoglobulin in human disease: a review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology. (2006) (597)
Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. (1972) (558)
Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution. (2004) (544)
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants. (1997) (521)
Treatment of adenosine deaminase deficiency with polyethylene glycol-modified adenosine deaminase. (1987) (423)
Genetic linkage of hyper-IgE syndrome to chromosome 4. (1999) (372)
Fungal infection in chronic granulomatous disease. The importance of the phagocyte in defense against fungi. (1981) (351)
Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival. (2002) (331)
Transplantation outcomes for severe combined immunodeficiency, 2000-2009. (2014) (326)
Anaphylactic reactions after gamma globulin administration in patients with hypogammaglobulinemia. Detection of IgE antibodies to IgA. (1986) (300)
Gastrointestinal pathology in patients with common variable immunodeficiency and X-linked agammaglobulinemia. (1996) (289)
The use of intravenous immune globulin in immunodeficiency diseases. (1991) (278)
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience. (2014) (263)
Transplantation of thymus tissue in complete DiGeorge syndrome. (1999) (252)
Persistent and fatal central-nervous-system ECHOvirus infections in patients with agammaglobulinemia. (1977) (246)
Mutations in the mu heavy-chain gene in patients with agammaglobulinemia. (1996) (230)
Primary immunodeficiency diseases due to defects in lymphocytes. (2000) (217)
Serum immunoglobulins. I. Levels in normal children and in uncomplicated childhood allergy. (1968) (207)
Thymic function after hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency. (2000) (205)
Abnormalities in the Regulation of Human IgE Synthesis (1978) (194)
Development of immunity in human severe primary T cell deficiency following haploidentical bone marrow stem cell transplantation. (1986) (183)
Correlation of milk precipitins with IgA deficiency. (1969) (183)
Transplantation of hematopoietic stem cells in human severe combined immunodeficiency: longterm outcomes (2011) (174)
Expression of the gene defect in X-linked agammaglobulinemia. (1986) (173)
Depression of cell-mediated immunity in atopic eczema. (1975) (173)
Serum IgD and IgE concentrations in immunodeficiency diseases. (1975) (172)
Immune reconstitution and survival of 100 SCID patients post-hematopoietic cell transplant: a PIDTC natural history study. (2017) (171)
In vivo inactivation of erythrocyte S-adenosylhomocysteine hydrolase by 2'-deoxyadenosine in adenosine deaminase-deficient patients. (1979) (154)
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. (2015) (151)
Transplantation immunology: solid organ and bone marrow. (2010) (150)
Cancer in primary immunodeficiency diseases: Cancer incidence in the United States Immune Deficiency Network Registry (2017) (149)
Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency. (1997) (148)
Unexpected effects of FERM domain mutations on catalytic activity of Jak3: structural implication for Janus kinases. (2001) (147)
Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome. (2000) (141)
Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases. (2004) (137)
Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts. (2014) (136)
Primary cellular immunodeficiencies. (2002) (134)
Use of intravenous gamma-globulin in antibody immunodeficiency: results of a multicenter controlled trial. (1982) (134)
Janus kinase 3 (JAK3) deficiency: clinical, immunologic, and molecular analyses of 10 patients and outcomes of stem cell transplantation. (2004) (124)
Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome. (2001) (124)
Jak3 and the pathogenesis of severe combined immunodeficiency. (2004) (122)
Pulmonary complications of primary immunodeficiencies. (2004) (121)
Complete DiGeorge syndrome: persistence of profound immunodeficiency. (1998) (120)
Transient hypogammaglobulinemia of infancy: review of the literature, clinical and immunologic features of 11 new cases, and long-term follow-up. (1978) (116)
SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery. (2018) (115)
Mutations in genes required for T-cell development:IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review (2004) (113)
Improving cellular therapy for primary immune deficiency diseases: recognition, diagnosis, and management. (2009) (110)
The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901 (2013) (105)
Defective cellular immunity associated with chronic mucocutaneous moniliasis and recurrent staphylococcal botryomycosis: immunological reconstitution by allogeneic bone marrow. (1968) (105)
Human IgE biosynthesis in vitro: studies with atopic and normal blood mononuclear cells and subpopulations. (1979) (100)
Clinical and immunologic features of selective IgA deficiency. (1975) (97)
The multiple causes of human SCID. (2004) (97)
Immunoglobulin G subclass deficiency: Fact or fancy? (2002) (97)
Hyper IgM Syndrome: a Report from the USIDNET Registry (2016) (97)
Natural killing in immunodeficient patients. (1978) (95)
Membrane receptors and in vitro responsiveness of lymphocytes in human immunodeficiency. (1974) (95)
Comparison of the efficacy of IGIV-C, 10% (caprylate/chromatography) and IGIV-SD, 10% as replacement therapy in primary immune deficiency. A randomized double-blind trial. (2003) (92)
Long-term clinical outcome of patients with severe combined immunodeficiency who received related donor bone marrow transplants without pretransplant chemotherapy or post-transplant GVHD prophylaxis. (2009) (91)
Management options for adenosine deaminase deficiency; proceedings of the EBMT satellite workshop (Hamburg, March 2006). (2007) (91)
Angelman syndrome: are the estimates too low? (1998) (89)
The hyper-IgE syndrome (2001) (88)
Inability of gestational hormones to account for the inhibitory effects of pregnancy plasmas on lymphocyte responses in vitro. (1975) (86)
The long quest for neonatal screening for severe combined immunodeficiency. (2012) (85)
Successful formation of a chimeric human thymus allograft following transplantation of cultured postnatal human thymus. (1997) (84)
Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency. (2014) (82)
A Novel Mutation in IFN-γ Receptor 2 with Dominant Negative Activity: Biological Consequences of Homozygous and Heterozygous States1 (2004) (81)
B-cell reconstitution for SCID: should a conditioning regimen be used in SCID treatment? (2013) (81)
Molecular form of adenosine deaminase in severe combined immunodeficiency. (1974) (80)
Thymic output, T-cell diversity, and T-cell function in long-term human SCID chimeras. (2009) (79)
Antibody responses to bacteriophage phi X174 in patients with adenosine deaminase deficiency. (1992) (77)
SAFETY AND PATIENT ACCEPTABILITY OF INTRAVENOUS IMMUNE GLOBULIN IN 10% MALTOSE (1980) (75)
Immunodeficiency diseases. (1987) (75)
Gene therapy for SCID—a complication after remarkable progress (2002) (73)
T Cell Repertoire Development in Humans with SCID After Nonablative Allogeneic Marrow Transplantation 1 (2003) (73)
Immunoglobulin prophylaxis in patients with antibody deficiency syndromes and anti-IgA antibodies (2004) (72)
Outcome of hematopoietic cell transplantation for DNA double‐strand break repair disorders (2018) (72)
Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: current status and critical needs. (2008) (72)
Recombinant human IL-4 induces IgE and IgG synthesis by normal and atopic donor mononuclear cells. Similar dose response, time course, requirement for T cells, and effect of pokeweed mitogen. (1990) (68)
Post-Transplantation B Cell Function in Different Molecular Types of SCID (2012) (67)
Correction of severe combined immunodeficiency by fetal liver cells. (1976) (67)
T−B+NK+ severe combined immunodeficiency caused by complete deficiency of the CD3ζ subunit of the T-cell antigen receptor complex (2007) (65)
Expansion of somatically reverted memory CD8+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus (2012) (65)
Primary Immune Deficiency Treatment Consortium (PIDTC) report. (2014) (64)
Advances in the understanding and treatment of human severe combined immunodeficiency (2000) (64)
ENHANCED BACTERICIDAL ACTIVITY OF PHAGOCYTES FROM PATIENTS WITH CHRONIC GRANULOMATOUS DISEASE IN THE PRESENCE OF SULPHISOXAZOLE (1975) (63)
Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency. (2021) (63)
Blocking of autologous and homologous leukocyte responses by human alloimmune plasmas: a possible in vitro correlate of enhancement. (1972) (63)
Human IgE synthesis in vitro: a reassessment. (1981) (62)
Primary immunodeficiency diseases: dissectors of the immune system (2002) (62)
Serum IgE concentrations and skin reactivity to anti-IgE antibody in IgA-deficient patients. (1971) (60)
Prenatal gene tranfer: scientific, medical, and ethical issues: a report of the Recombinant DNA Advisory Committee. (2000) (59)
Heterogeneity of lymphocyte subpopulations in severe combined immunodeficiency. Evidence against a stem cell defect. (1976) (58)
Antibody responses to protein, polysaccharide, and phi X174 antigens in the hyperimmunoglobulinemia E (hyper-IgE) syndrome. (1991) (57)
Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiency. (1993) (56)
Digital microfluidics: a future technology in the newborn screening laboratory? (2010) (56)
A nonsense mutation in IKBKB causes combined immunodeficiency. (2014) (56)
B-cell function in severe combined immunodeficiency after stem cell or gene therapy: a review. (2010) (55)
Cutaneous Complications of BCG Vaccination in Infants with Immune Disorders: Two Cases and a Review of the Literature (2001) (53)
Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry. (2017) (51)
Pharmacokinetics and tolerability of a new intravenous immunoglobulin preparation, IGIV‐C, 10% (Gamunex™, 10%) (2003) (51)
Serum immunoglobulin concentrations during normal pregnancy (1971) (50)
Characterization of precipitating antibodies to ruminant serum and milk proteins in humans with selective IgA deficiency. (1971) (50)
Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature (2016) (49)
Serum immunoglobulins. 3. Abnormalities associated with chronic urticaria in children. (1967) (49)
Abnormalities of leukotaxis in atopic dermatitis. (1977) (48)
Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency. (1995) (48)
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings. (1990) (48)
Demonstration of abnormalities in expression of thymic epithelial surface antigens in severe cellular immunodeficiency diseases. (1983) (47)
Anaphylactic reactions to plasma infusions in patients with hypogammaglobulinemia and anti-IgA antibodies. (1977) (47)
Primary immunodeficiency or not? Making the correct diagnosis. (2006) (46)
Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors (2018) (46)
Lymphocyte responses to purified ragweed allergens in vitro. I. Proliferative responses in normal, newborn, agammaglobulinemic, and atopic subjects. (1977) (45)
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis. (1990) (45)
Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency. (2011) (43)
The genetic landscape of severe combined immunodeficiency in the United States and Canada in the current era (2010-2018). (2019) (43)
A historical review of bone marrow transplantation for immunodeficiencies. (2004) (43)
Symptomatic giardiasis in three patients with X-linked agammaglobulinemia. (1982) (43)
Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Stem Cell Transplantation (HCT) for Severe Combined Immunodeficiency Patients: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects afte (2017) (43)
Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey (2020) (42)
Unusual clinical and immunologic manifestations of transplacentally acquired maternal T cells in severe combined immunodeficiency. (2007) (42)
Precipitins to Candida albicans in chronic mucocutaneous candidiasis studied by crossed immunoelectrophoresis with intermediate gel. Correlation with clinical and immunological findings. (1974) (42)
CD45-deficient severe combined immunodeficiency caused by uniparental disomy (2012) (41)
Primary immunodeficiency disorders in pediatric patients: clinical features and imaging findings. (2001) (40)
Incompatible Bone-Marrow Transplantation in Lymphopenic Immunologic Deficiency (1971) (38)
T-B+NK+ severe combined immunodeficiency caused by complete deficiency of the CD3zeta subunit of the T-cell antigen receptor complex. (2007) (37)
Development of IgA and IgG2 subclass deficiency after sulfasalazine therapy. (1986) (37)
Why Newborn Screening for Severe Combined Immunodeficiency Is Essential: A Case Report (2010) (36)
Role of JAK3 in CD40-mediated signaling. (1998) (36)
Severe combined immunodeficiency with leukopenia (reticular dysgenesis) in siblings: immunologic and histopathologic findings. (1976) (36)
Hyperimmunoglobulinemia E syndrome: radiographic observations. (1979) (34)
Hereditary Alterations in the Immune Response: Coexistence of ‘Agammaglobulinemia', Acquired Hypogammaglobulinemia and Selective Immunoglobulin Deficiency in a Sibship (1968) (34)
Specificity and Function of “Natural” Antibodies in Immunodeficient Subjects: Clues to B Cell Lineage and Development (1997) (34)
Growth-dependent regulation of cellular ceramides in human T-cells. (1994) (33)
Mononuclear cells from patients with the hyper-IgE syndrome produce little IgE when they are stimulated with recombinant human interleukin-4. (1991) (33)
Transplantation immunology: Organ and bone marrow (2003) (33)
Rapid infusion of Sandoglobulin in patients with primary humoral immunodeficiency. (1991) (33)
Humoral immunodeficiency. (1986) (33)
Correction of purine nucleoside phosphorylase deficiency by transplantation of allogeneic bone marrow from a sibling. (1996) (32)
Multicenter, double-blind, placebo-controlled trial of terfenadine suspension in the treatment of fall-allergic rhinitis in children. (1986) (32)
Multicenter Crossover Comparison of the Safety and Efficacy of Intraglobin-F with Gamimune-N, Sandoglobulin, and Gammagard in Patients with Primary Immunodeficiency Diseases (2004) (31)
Practice parameters for the diagnosis and management of immunodeficiency. The Clinical and Laboratory Immunology Committee of the American Academy of Allergy, Asthma, and Immunology (CLIC-AAAAI) (1996) (31)
Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiency. (1987) (31)
Breakthroughs in the understanding and therapy of primary immunodeficiency. (1994) (31)
Variability in B cell maturation and differentiation in X-linked agammaglobulinemia. (1986) (30)
Serum immunoglobulins. II. Levels in children subject to recurrent infection. (1968) (30)
Abnormal development of thymic dendritic and epithelial cells in human X-linked severe combined immunodeficiency. (2004) (29)
Recommendations for Screening and Management of Late Effects in Patients with Severe Combined Immunodeficiency after Allogenic Hematopoietic Cell Transplantation: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Ped (2017) (29)
IMMUNODEFICIENCY (1975) (28)
Modified MHC restriction of donor-origin T cells in humans with severe combined immunodeficiency transplanted with haploidentical bone marrow stem cells. (1989) (28)
Gene therapy for human SCID: Dreams become reality (2000) (28)
Variable phenotypic expression of mutations in genes of the immune system. (2005) (28)
B-cell differentiation and IL-21 response in IL2RG/JAK3 SCID patients after hematopoietic stem cell transplantation. (2018) (28)
Positive Family History, Infection, Low Absolute Lymphocyte Count (ALC), and Absent Thymic Shadow: Diagnostic Clues for All Molecular Forms of Severe Combined Immunodeficiency (SCID). (2015) (27)
Selective immunoglobulin deficiency associated with thymic alymphoplasia. (1967) (27)
Variability of IgE protein measurement in cell-culture supernatants: results from a multicenter collaborative study. (1986) (27)
A cell culture system that enhances mononuclear cell IgE synthesis induced by recombinant human interleukin-4. (1990) (27)
Clinical application of whole-genome sequencing in patients with primary immunodeficiency. (2015) (26)
Successful treatment of autoimmune hemolytic anemia in common variable immunodeficiency with high-dose intravenous gamma globulin. (1987) (26)
Accelerated development of immunity following transplantation of maternal marrow stem cells into infants with severe combined immunodeficiency and transplacentally acquired lymphoid chimerism. (1988) (26)
Abnormalities in the regulation of human IgE synthesis. (1982) (26)
Diagnostic Immunization with Bacteriophage ΦX 174 in Patients with Common Variable Immunodeficiency/Hypogammaglobulinemia (2014) (25)
Severe combined immunodeficiency with natural killer-cell predominance: abrogation of graft-versus-host disease and immunologic reconstitution with HLA-identical bone marrow cells. (1984) (25)
Plasma therapy in immunodeficiency diseases. (1972) (24)
Developmental immunology and the immunodeficiency diseases. (1982) (24)
Long term use of intravenous immune globulin in patients with primary immunodeficiency diseases: Inadequacy of current dosage practices and approaches to the problem (1982) (24)
Iron deficiency anemia: its relationship to infection susceptibility and host defense. (1975) (24)
Prevalence of lymphocytopenia in severe combined immunodeficiency. (1990) (24)
27. Transplantation immunology: organ and bone marrow. (2003) (24)
30-Year Review of Pediatric- and Adult-Onset CVID: Clinical Correlates and Prognostic Indicators (2019) (22)
Normalization of the Peripheral Blood T Cell Receptor Vβ Repertoire After Cultured Postnatal Human Thymic Transplantation in DiGeorge Syndrome (1997) (21)
Allergic skin disorders. (1987) (21)
IgA IN SALIVA OF BREAST-FED AND BOTTLE-FED INFANTS (1980) (20)
Use of a new chemically modified intravenous IgG preparation in severe primary humoral immunodeficiency: clinical efficacy and attempts to individualize dosage. (1984) (20)
Combined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis. (2015) (19)
Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers (2020) (19)
Diagnosis of 22q11.2 Deletion Syndrome and Artemis Deficiency in Two Children with T-B-NK+ Immunodeficiency (2012) (18)
Modified responses to recipient and donor B cells by genetically donor T cells from human haploidentical bone marrow chimeras. (1987) (18)
Candida meningitis in two children with severe combined immunodeficiency. (1984) (18)
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del (1998) (17)
Antibody-dependent cellular cytotoxicity in primary immunodeficiency diseases and with normal leukocyte subpopulations. Importance of the type of target. (1978) (17)
HUMAN SEVERE COMBINED IMMUNODEFICIENCY (SCID): GENETIC, PHENOTYPIC AND FUNCTIONAL DIVERSITY IN 95 INFANTS. • 41 (1996) (17)
Agammaglobulinemia, neutropenia, fever, and abdominal pain. (1973) (17)
Hematopoietic Stem Cell Transplantation for CD40 Ligand Deficiency: Single Institution Experience (2015) (17)
Gastroesophageal reflux and severe combined immunodeficiency. (1997) (16)
Mutation Analysis of IL 2 RG in Human X-Linked Severe Combined Immunodeficiency (1997) (15)
Bone marrow and thymus transplantation in ataxia-telangiectasia. (1975) (15)
Long-term outcome of non-ablative booster BMT in patients with SCID. (2013) (15)
Studies of human bone marrow treated with soybean lectin and sheep erythrocytes: stepwise analysis of cell morphology, phenotype and function. (1987) (14)
Monoclonal immunoglobulin-secreting lymphoma in a patient with severe combined immunodeficiency disease. (1982) (14)
The functions and measurement of human B- and T-lymphocytes. (1976) (13)
Epstein-Barr–associated Leiomyomatosis and T-cell Chimerism After Haploidentical Bone Marrow Transplantation for Severe Combined Immunodeficiency Disease (2007) (13)
EXTREME HYPERIMMUNOGLOBULINEMIA E AND UNDUE SUSCEPTIBILITY TO INFECTION (1972) (13)
Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry (2020) (13)
Treatment options for genetically determined immunodeficiency (2003) (13)
Graft versus graft and graft versus host reactions after HLA‐identical bone marrow transplantation in a patient with severe combined immunodeficiency with transplacentally acquired lymphoid chimerism (1991) (13)
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online. (1998) (12)
The use of nonhuman primates for studies of reagin (1965) (12)
Evaluation of serum immunoglobulin concentrations in the perinatal period by use of a standardized method of measurement. (1969) (12)
Lymphopenic immunologic deficiency in identical twins: lymphocyte allografting and graft-versus-host disease following treatment with albumin-gradient-separated paternal bone marrow cells. (1971) (12)
Practice Parameters for the Diagnosis and Management of Immunodeficiency (1997) (12)
Advances in the diagnosis and treatment of primary immunodeficiency diseases. (1986) (12)
HLA antigens in primary immunodeficiency diseases. (1977) (11)
Colonic nodular lymphoid hyperplasia in a child with antibody deficiency and near-normal immunoglobulins. (1981) (11)
Clinical Immunology-Allergy in Paediatric Medicine (1975) (10)
Development of multiple monoclonal serum immunoglobulins (multiclonal gammopathy) following both HLA-identical unfractionated and T cell-depleted haploidentical bone marrow transplantation in severe combined immunodeficiency (1990) (10)
Lentiviral Gene Therapy with Autologous Hematopoietic Stem and Progenitor Cells (HSPCs) for the Treatment of Severe Combined Immune Deficiency Due to Adenosine Deaminase Deficiency (ADA-SCID): Results in an Expanded Cohort (2019) (10)
Mechanism of pokeweed mitogen inhibition of rhIL-4-induced human IgE synthesis. (1992) (10)
Tolerance and immunity after sequential lung and bone marrow transplantation from an unrelated cadaveric donor. (2015) (9)
T Lymphocytes, B Lymphocytes, and Natural Killer Cells (2011) (9)
Successful immune reconstitution in severe combined immunodeficiency despite Epstein-Barr virus and cytomegalovirus infections. (1985) (8)
Assessing inheritance of agammaglobulinemia. (1994) (8)
Primary Defects of Antibody Production (2011) (8)
Primary Combined Antibody and Cellular Immunodeficiencies (2011) (8)
Impaired antibody response to polysaccharides in association with functional asplenia. (1989) (8)
Lymphocyte responses to ragweed antigens from different sources. (1979) (8)
Advances in the correction of immunodeficiency by bone marrow transplantation. (1987) (8)
Appearance of multiple benign paraproteins during early engraftment of soy lectin T cell-depleted haploidentical bone marrow cells in severe combined immunodeficiency (1986) (8)
Immunization Of The Immunocompromised Host (1998) (7)
severe combined immunodeficiency caused by complete deficiency of the CD 3 subunit of the T-cell antigen receptor complex (2007) (7)
T cells and T-cell subsets in a large population of patients with primary immunodeficiency. (1983) (7)
Reactivity of Human IgG Antibodies in Primate and Guinea Pig Passive Anaphylaxis (1966) (6)
Successful treatment of disseminated BCG in a patient with severe combined immunodeficiency. (2015) (6)
Outcomes Following Treatment for Adenosine Deaminase Deficient Severe Combined Immunodeficiency: A Report from the PIDTC. (2022) (6)
Pulmonary coin lesion caused by Neisseria mucosa in a child with chronic granulomatous disease (1987) (6)
161. In vitro studies of human IgE biosynthesis (1978) (6)
Individualization of gamma globulin dosage in patients with humoral immunodeficiency. (1983) (6)
Serum immunogbulin cocentrations during normal pregnancy. (1971) (5)
Common "allergic' skin diseases. (1982) (5)
702 EVIDENCE FOR EXCESSIVE T SUPPRESSOR CELL ACTIVITY IN X-LINKED IMMUNODEFICIENCY WITH HYPER-IgM (1978) (5)
Long-term Clinical Outcomes of Severe Combined Immunodeficiency Patients Given Nonablative Marrow Transplants (2021) (5)
The development of homologous skin-sensitizing antibodies in experimental thyroiditis. (1967) (5)
Clinical and imaging considerations in primary immunodeficiency disorders: an update (2016) (5)
Conversations with Founders of the Field of Human Inborn Errors of Immunity (2020) (5)
The diagnosis of severe combined immunodeficiency: Implementation of the PIDTC 2022 Definitions. (2022) (5)
γ-Globulin replacement (1985) (4)
Immunodeficiency diseases. (1992) (4)
Certification in diagnostic laboratory immunology. (1986) (4)
Early Hematopoietic Cell Transplant (HCT) Outcomes of Children with Severe Combined Immunodeficiency Disease (SCID): The First Seventy Four Patients of the Primary Immune Deficiency Treatment Consortium (PIDTC) Prospective Study 6901 (2015) (4)
In vitro studies of IgE synthesis by human blood mononuclear cells. (1981) (4)
Donor type natural killer cells after haploidentical T cell-depleted bone marrow stem cell transplantation in a patient with adenosine deaminase-deficient severe combined immunodeficiency. (1991) (4)
The Natural History of Children with Severe Combined Immunodeficiency Disease (SCID): The First Fifty Patients of the Primary Immune Deficiency Treatment Consortium (PIDTC) Prospective Study 6901 (2013) (4)
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions. (2022) (4)
Nutritional and antigenic effects of two bovine milk preparations in infants. (1966) (4)
Augmented Immunoglobulin E Synthesis in Primary Immunodeficiency (1979) (3)
Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance. (1983) (3)
69 Comparison of plasma histamine (H) and tryptase levels following double-blind placebo-controlled food challenges (DBPCFC'S) in patients with asthma (AS) and/or atopic dermatitis (AD) (1988) (3)
Medusa cells: The morphology and cytochemistry of common amoeboid variants of eosinophils (1980) (3)
Incompatible bone marrow transplantation in lymphopenic immunologic deficiency (1971) (3)
Natural-killer-cell function and bone marrow transplantation. (1986) (3)
Poor T Cell Reconstitution at 100 Days after T Cell-Replete Hematopoietic Cell Transplantation (HCT) for SCID Is Associated with Later Risk of Death or Need for 2nd Transplant in the 6901 Prospective Study of the Pidtc (2016) (3)
Ex Vivo Gene Therapy of a Preadolescent with X-Linked Severe Combined Immunodeficiency. (2004) (3)
Diagnostic laboratory immunology: a subspecialty that encompasses clinical as well as laboratory immunology. (1991) (3)
Progress toward less toxic conditioning. (2016) (3)
131 Antibody deficiency syndromes with anti-IgA antibodies and successful immunoglobulin prophylaxis (1985) (2)
Immunologic studies before and after splenectomy in a patient with the Wiskott-Aldrich syndrome (2004) (2)
133 Variability in the quantitation of IgE protein in cell culture supernatants (1985) (2)
Evaluation of Suspected Immunodeficiency (2011) (2)
Five Great Allergists (2005) (2)
The Effect of Natural Killer Cell Killer Ig-Like Receptor Alloreactivity on the Outcome of Bone Marrow Stem Cell Transplantation for Severe Combined Immunodeficiency (SCID) (2007) (2)
Statement by the Executive Committee (1978) (2)
Outcome of domino hematopoietic stem cell transplantation in human subjects: An international case series. (2018) (2)
273 Modified T cell MHC restriction following successful haploidentical bone marrow stem cell transplantation in severe combined immunodeficiency disease (SCID) (1988) (2)
Adenosine Deaminase Deficiency: Recent Observations Pertinent to Investigation of the Physiologic Role of Adenosine in Man (1987) (2)
276 Antigen-specific humoral and cellular immune responses during treatment of adenosine deaminase deficient severe combined immunodeficiency (ADA-SCID) with polyethylene glycol-modified bovine adenosine deaminase (PEG-ADA) (1988) (2)
Bone marrow transplantation for CVID‐like humoral immune deficiency associated with red cell aplasia (2016) (2)
The long and the short of telomeres in bone marrow recipient SCID patients (2011) (2)
Primary Defects of Cellular Immunity (2011) (2)
472 Successful treatment of invasive aspergillus infection with itraconazole in chronic granulomatous disease (CGD) (1988) (2)
Genotype, Phenotype and T Cell Counts at One Year Predict Survival and Long Term Immune Reconstitution after Transplantation in Severe Combined Immune Deficiency (SCID)—The Primary Immune Deficiency Treatment Consortium (PIDTC) (2017) (2)
Anaphylactic reactions and anti-IgA antibodies in common variable agammaglobulinemia: IgA deficient plasma treatment (1982) (2)
Autologous Ex Vivo Lentiviral Gene Therapy for the Treatment of Severe Combined Immune Deficiency Due to Adenosine Deaminase Deficiency (ADA-SCID) (2019) (2)
Comparison of Bitolterol Mesylate and Isoproterenol by Metered-Dose Inhaler for Regular, Long-Term Treatment in Asthmatic Children (1989) (2)
270 B cell function in severe combined immunodeficiency (SCID) Following HLA-identical and haploidentical marrow transplantation (1988) (1)
Role of JAK 3 in CD 40-Mediated Signaling (1998) (1)
Alpha-fetoprotein levels in immunodeficiency. (1986) (1)
275 Immunogenecity of polyethylene glycol-modified bovine adenosine deaminase (PEG-ADA) (1988) (1)
M285 ADULT MALE WITH STAT3 GAIN-OF-FUNCTION MUTATION PREVIOUSLY DIAGNOSED AS COMMON VARIABLE IMMUNODEFICIENCY (2019) (1)
SCID: A Pediatric Emergency. (2019) (1)
Transplantation Outcomes for Children with Severe Combined Immune Deficiency (SCID) Have Improved over Time: A 36-Year Summary Report By the Primary Immune Deficiency Treatment Consortium (PIDTC) (2020) (1)
Food Allergy-Reply (1983) (1)
Effects of hydrocortisone (HC) on IgE synthesis by cultured human mononuclear cells (MNC) (1982) (1)
Immune thrombocytopenia treated with high-dose intravenous gamma globulin and corticosteroids in two patients with Wiskott-Aldrich syndrome (1988) (1)
Advances in asthma/allergy. (1979) (1)
Hyper IgM Syndrome: a Report from the USIDNET Registry (2016) (1)
Implications of "certification in diagnostic laboratory immunology" for the training and practice in allergy-immunology. (1983) (1)
American Pediatric Society Presidential Address 2000: Reflections on the 20th and 21st Centuries (2002) (1)
Tandem HLA-Mismatched Cadaveric Unrelated Donor Lung Transplant Followed by CD3-and CD19-Depleted Bone Marrow Transplant From the Same Donor Permits Withdrawal of Systemic Immunosuppression with Graft Acceptance and Functional Immune Reconstitution (2011) (1)
339 Appearance of multiple paraproteins during early engraftment of soy lectin T cell depleted haploidentical bone marrow cells in severe combined immunodeficiency (SCID) (1985) (1)
Regulation of IgE synthesis: introduction. (1981) (1)
Workshop 7: Special pediatric problems (1986) (1)
Retrospective Study of 240 Patients with Severe Combined Immunodeficiency Transplanted from 2000-2009: A Report from the Primary Immune Deficiency Treatment Consortium of North America (2014) (1)
Screening for primary immunodeficiency diseases and follow-up testing. (2016) (1)
Conversations with Founders of the Field of Human Inborn Errors of Immunity (2020) (0)
339 Deficient responses to polysaccharide antigens and to bacteriophage φ × 174 in association with functional asplenia (1988) (0)
Letters to the Editor (1967) (0)
178 T cells and subsets in a large population of primary immunodeficiency patients (1983) (0)
When the Patient Asks: Q: Should my son get an HPV vaccine? (2011) (0)
Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature (2016) (0)
Possible Immunoglobulin Deficiency-Reply (1983) (0)
180 Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance: Effects of bone marrow transplantation (1983) (0)
IDF Medical Advisory Committee Resolution on Product Choice for Immunoglobulin Replacement Therapy (2011) (0)
Lymphocyte responses to antigen E in normal and in treated and untreated ragweed sensitive subjects (1976) (0)
A study of cancer incidence in the most common immunodeficiency, common variable immunodeficiency (CVID): 243 (2019) (0)
Natural killer (NK) cell ontogeny in severe combined immunodeficiency (SCID) after bone marrow transplantation (BMT) (2002) (0)
Post-Transplantation B Cell Function in Different Molecular Types of SCID (2012) (0)
American Pediatric Society’s 2014 John Howland Award acceptance lecture: saving lives through early diagnosis (2014) (0)
common variable immunodeficiency syndrome Alterations of the X-linked lymphoproliferative disease geneSH2D1A in (2013) (0)
IDF MEDICAL ADVISORY COMMITTEE (2013) (0)
B Cell Reconstitution for SCID: Should a conditioning regimen be used in the treatment of SCID? (2013) (0)
Prevalence of X-linked lymphoproliferative (XLP) disease mutation among male patients with CVID (2002) (0)
Subcutaneous infusion of immune globulin in an infant with severe combined immunodeficiency (SCID) (2005) (0)
Natural Killer T (NKT) Cell Development in Severe Combined Immunodeficiency (SCID) After T Cell Depleted Haploidentical Bone Marrow Transplantation (BMT) (2006) (0)
Mitogen induced DNA synthetic responses of lymphocyte subpopulations in partial DiGeorge syndrome (1977) (0)
977 Expression of unique cell surface proteins of B cells of patients with severe combined immunodeficiency (SCID) (1996) (0)
Functional characterization of natural killing against a mouse fibrosarcoma target. Abstr. (1978) (0)
IgG Subclass Deficiency Table 1 : Property of IgG Subclasses Property IgG (1999) (0)
Intracellular cytokine production by T cells in SCID infants with time post-bone marrow transplantation (BMT) (2004) (0)
Chapter 5 – Studies of Patients with Severe Cellular and Humoral Immunodeficiency Diseases Using Monoclonal Antibodies1 (1983) (0)
Clinical and Immunologic Manifestations of Transplacentally Acquired Maternal T-Cells in SCID (2006) (0)
Distinctive clinical and laboratory features of autosomal-recessive hyper IgM syndrome (2002) (0)
Letters to the Editor. (2019) (0)
Aberrant T-cell exhaustion in SCID survivors with poor T-cell reconstitution post transplant. (2022) (0)
Expression of gene defect in x linked agammaglobulinemia is intrinsic to the b cell lineage (1986) (0)
Correction to: Infections in Infants with SCID: Isolation, Infection Screening and Prophylaxis in PIDTC Centers (2020) (0)
Diagnosis of 22q11.2 Deletion Syndrome and Artemis Deficiency in Two Children with T-B-NK+ Immunodeficiency (2012) (0)
416 Effects of allergy/asthma drugs on IgE synthesis (1996) (0)
A Single-Center Review of Severe Combined Immune Deficiency (SCID) Newborn Screening (NBS) Data in the Neonatal Intensive Care Unit (NICU) (2023) (0)
SPECIAL ARTICLE American Pediatric Society Presidential Address 2000: Reflections on the 20th and 21st Centuries (2002) (0)
Who should get SMA carrier screening? (2010) (0)
Human SCID and its Treatment (2003) (0)
Family History and Low Absolute Lymphocyte Count (ALC) as Diagnostic Clues for Severe Combined Immunodeficiency (SCID) (2008) (0)
Marrow Transplantation with SCID After Nonablative Allogeneic T Cell Repertoire Development in Humans (2003) (0)
EBV-associated leiomyomas following haploidentical transplantation for X-linked severe combined immunodeficiency disease (2005) (0)
Noninvasive prenatal testing strategy detects maple syrup urine disease in a fetus (2014) (0)
303 Synovial lymphocyte phenotypes in the inflammatory arthritis of x-linked agammaglobulinemia (1983) (0)
Should my son get an HPV vaccine? (2011) (0)
Correction to: Infections in Infants with SCID: Isolation, Infection Screening and Prophylaxis in PIDTC Centers (2020) (0)
Accelerated development ofimmunityfollowing transplantation of maternal marrow stemcells intoinfants withseverecombined immunodeficiency andtransplacentally acquired lymphoidchimerism (1988) (0)
CIS PRESIDENTIAL AWARD (2013) (0)
Long term Outcome of Non-Ablative Booster Bone Marrow Transplantation in Patients with Severe Combined Immunodeficiency (2013) (0)
Successful Staged Combined Lung-Stem Cell Transplant (2011) (0)
Presidential address. Reflections on the 1970s and a look to the future. (1980) (0)
The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901 (2013) (0)
On Assessing Immunocompetence (2009) (0)
and improved survival immunodeficiency in the neonatal period leads to superior thymic output Hematopoietic stem cell transplantation for severe combined (2013) (0)
Interleukin-7 receptor a chain mutations in 13 patients with severe combined immunodeficiency* (2003) (0)
788 Haploidentical T cell-depleted bone marrow transplantation into a premature infant with X-linked severe combined immunodeficiency (X-SCID) (2000) (0)
PD-1 IS ESSENTIAL TO INDUCE PERIPHERAL CD8 T CELL TOLERANCE IN ALLOGENEIC BONE MARROW TRANSPLANTATION (2006) (0)
A Sensitive Microtiter Test for Detecting Rheumatoid Factor in Children (1970) (0)
Midnight in Moscow (2011) (0)
787 Successful and rapid immune reconstitution using a pregnant donor for T-cell depleted haploidentical bone marrow transplantation for a patient with severe combined immunodificiency (2000) (0)
News Items / Obituary (1966) (0)
HSCT using carrier donors for CD40L deficiency results in excellent immune function and higher CD40L expression in cTfh (2022) (0)
2 CD 4 + Invariant Natural Killer T Cells Protect from Acute Graft-Versus-Host Disease Lethality through a Dramatic Expansion of Donor-Derived CD 4 + FoxP 3 + Regulatory T Cells (2014) (0)
SCID (2019) (0)
Responses to recipient and donor B cells by genetically donor T cells from human haploidentical chimeras (1986) (0)
Long-term Clinical Outcome of Patients with Severe Combined Immunodeficiency (SCID) after Non-Ablative Related Donor Bone Marrow Transplantation (2008) (0)
Emergence of CD45RA+ and CD62L+ Blood T Cells in Infants with Severe Combined Immunodeficiency (SCID) Given HLA-Identical or Haploidentical T Cell-Depleted Bone Marrow Stem Cells (1999) (0)
Specific Antibody Synthesis in Patients with Immunoglobulin Deficits (2009) (0)
Interferon-γ receptor-2 deficiency presenting with cytomegalovirus infection (2003) (0)
50 Years Ago in TheJournal ofPediatrics: Nutritional and Antigenic Effects of 2 Bovine Milk Preparations in Infants. (2016) (0)
784 Thymic output after non-ablative allogeneic hematopoietic stem cell transplantation in infants with severe combined immunodeficiency (SCID) (2000) (0)
Human cord blood (CB) lymphocyte T helper and suppressor phenotypes, immunoglobulin (IG) production, and effects on normal adult IG production (1982) (0)
Advances in CRT (2012) (0)
836 Development of normal T-cell function and TCR repertoire after post-natal thymic transplantation for DiGeorge syndrome (1996) (0)
analyses of 10 patients and outcomes of stem cell transplantation Janus kinase 3 (JAK3) deficiency: clinical, immunologic, and molecular (2013) (0)
HEMOLYTIC ANEMIA (HA) IN A CHILD WITH ADENOSINE DEAMINASE (ADA) DEFICIENCY (1984) (0)
Atopic Dermatitis—A New Therapeutic Regimen-Reply (1983) (0)
Comparison of outcomes of hematopoietic stem cell transplant without chemotherapy conditioning using matched sibling and unrelated donors for treatment of SCID (2014) (0)
34-OR: Impact of alloreactivity of killer Ig-like receptors in the outcome of bone marrow stem cell transplantation for severe combined immunodeficiency (2006) (0)
Plasma therapy in immunodeficiency diseases. (1972) (0)
Characterization of pediatric onset common variable immunodeficiency (CVID) in a large cohort (2018) (0)
A Primary Immune Deficiency Treatment Consortium (PIDTC) Study of Chronic and Late Onset Medical Complications after Initial Hematopoietic Cell Transplantation (HCT) for Severe Combined Immunodeficiency Disease (SCID) (2022) (0)
64 Lymphocyte responses to pollen allergens: Effect of polymerized allergen immunotherapy (1985) (0)
Occurrence and Significance of Lymphopenia in the NICU, PICU and Well Baby Nursery (2010) (0)
Outcomes after Hematopoietic Cell Transplant and Gene Therapy for Adenosine Deaminase (ADA) Severe Combined Immune Deficiency: A Combined Analysis from the Primary Immune Deficiency Treatment Consortium (PIDTC) 6901 and 6902 Studies (2022) (0)
Retroviral Gene Transfer of Human Adenosine Deaminase into Hematopoietic Cells (1990) (0)
Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers (2020) (0)
Identification of dysregulated cytokine networks in human severe combined immunodeficiency using antibody-based microarrays for protein profiling (2003) (0)
CD45 Deficiency Caused by Uniparental Disomy, a Novel Cause of Severe Combined Immunodeficiency (2012) (0)
Letters to the Editor (1968) (0)
Phenytoin induced IgA suppression in children with seizure disorders (1982) (0)
Whole-Exome Sequencing Reveals IKBKB As a Cause of Combined Immunodeficiency (2014) (0)
960 DEVELOPMENT OF IMMUNITY IN SEVERE PRIMARY T CELL DEFICIENCY FOLLOWING HAPLOIDENTICAL STEM CELL TRANSPLANTATION (1985) (0)
BONE MARROW TRANSPLANTATION FOR SEVERE COMBINED IMMUNODEFICIENCY: ANALYSIS AT 15 YEARS ♦ 40 (1997) (0)
adenosine deaminase deficiency Antibody responses to bacteriophage phi X174 in patients with (2011) (0)
Ex vivo gene therapy of two children with X-linked severe combined immunodeficiency (2005) (0)
Next Generation Sequencing May Be More Efficient and Economical Than Targeted Gene Testing in Patients with Primary Immune Deficiency (PID) (2013) (0)
828 Deficiency of janus kinase 3 (Jak3) protein in severe combined immunodeficiency (SCID) (1996) (0)
Natural killer (NK) cells and bone marrow transplant (BMT) in severe combine combined immunodeficiency (SCID) (2004) (0)
CD4+CD25high T regulatory cells in SCID patients post-bone marrow transplantation (BMT) (2005) (0)
1003 SUCCESSFUL TREATMENT OF AUTOIMMUNE HEMOLYTIC ANEMIA (AIHA) IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) WITH HIGH-DOSE INTRAVENOUS IMMUNE SLOBULIN (IVIS) (1985) (0)
Michael M. Frank: February 28, 1937–August 1, 2019 (2019) (0)
Successful HLA-identical bone marrow transplantation in a patient with interferon-γ receptor 2 deficiency and disseminated Mycobacterium avium complex infection☆ (2004) (0)
500 Genetically-determined T cell deficiency: Clinical and laboratory profiles of 76 infants (1991) (0)
Demonstration of abnormalities in expression of thymic epithelial surface antigens in severe cellular immunodeficiency diseases. (1983) (0)
72 – Primary Immunodeficiency Diseases (2014) (0)
967 EFFECTS HYDROCORTISONE AND THEOPHYLLINE CN MONONUCLEAR CELL SUPERNATANT IgE CONCENTRATIONS (1981) (0)
Letters to the Editor (2014) (0)
280 IgE synthesis by newborn B cells stimulated with recombinant IL-4 (rhIL-4) with and without hydrocortisone (HC) (1991) (0)
333 Anaphylactic reactions in common variable agammaglobulinemia (CVA): Detection of IgE and IgG antibodies in an ELISA assay (1985) (0)
Severe Combined Immunodeficiency Caused by Complete Deficiency of the CD 3 ζ Subunit of the T Cell Antigen Receptor Complex Running Title : Human SCID Due to Complete CD 3 ζ Deficiency (2006) (0)
Event Free Survival in Severe Combined Immune Deficiency (SCID) Infants after Conditioned Umbilical Cord Blood Transplantation (UCBT) Benefits from Omitting Serotherapy (2023) (0)

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