Frederick S. Rosen

Frederick S. Rosen's AcademicInfluence.com Rankings

Frederick S. Rosen

Biology

#4472

World Rank

#6662

Historical Rank

Immunology

#192

World Rank

#201

Historical Rank

biology Degrees

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Biology

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Frederick S. Rosen's Published Works

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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

Regulation of the B cell response to T-dependent antigens by classical pathway complement. (1996) (411)
Hereditary Angioneurotic Edema: Two Genetic Variants (1965) (398)
Wiskott–Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses (2002) (306)
Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. (1996) (302)
Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3). (1970) (287)
Aberrations of suppressor T cells in human graft-versus-host disease. (1979) (270)
Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema. (1971) (252)
Primary immunodeficiencies. Report of a World Health Organization Committee. (1971) (251)
Persistent and fatal central-nervous-system ECHOvirus infections in patients with agammaglobulinemia. (1977) (246)
Complete correction of the Wiskott-Aldrich syndrome by allogeneic bone-marrow transplantation. (1978) (244)
AIDS--an immunologic reevaluation. (1984) (239)
Homozygous deficiency of C3 in a patient with repeated infections. (1972) (234)
Tranexamic acid therapy in hereditary angioneurotic edema. (1972) (227)
Severe combined immunodeficiency and adenosine deaminase deficiency. (1973) (225)
Selective gamma-g globulin deficiencies in patients with recurrent pyogenic infections. (1970) (224)
THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUM THE ROLE OF COMPLEMENT COMPONENTS AND TWO COFACTORS (1969) (209)
Abnormalities of immunoregulatory T cells in disorders of immune function. (1979) (205)
Primary immunodeficiency diseases: an update. (2004) (202)
Alper CA, Rosen FS: Studies of the in vivo behavior of human C'3 in normal subjects and patients. (1967) (198)
Heterogeneity of "acquired" or common variable agammaglobulinemia. (1974) (191)
Endotoxin shock in antibody-deficient mice: unraveling the role of natural antibody and complement in the clearance of lipopolysaccharide. (1997) (191)
Graft-versus-host disease after intrauterine and exchange transfusions for hemolytic disease of the newborn. (1974) (187)
The primary immunodeficiencies: first of two parts (1984) (182)
THE INTERACTION BETWEEN HUMAN MONOCYTES AND RED CELLS SPECIFICITY FOR IGG SUBCLASSES AND IGG FRAGMENTS (1970) (179)
Deficiency of a granulocyte-membrane glycoprotein (gp150) in a boy with recurrent bacterial infections. (1982) (178)
ACTION OF COMPLEMENT IN HEREDITARY ANGIONEUROTIC EDEMA: THE ROLE OF C'1-ESTERASE. (1964) (177)
Reconstitution after transplantation with T-lymphocyte-depleted HLA haplotype-mismatched bone marrow for severe combined immunodeficiency. (1982) (176)
Recurrent bacterial infections and dysgamma-globulinemia: deficiency of 7S gamma-globulins in the presence of elevated 19S gamma-globulins. Report of two cases. (1961) (164)
WIP is a chaperone for Wiskott–Aldrich syndrome protein (WASP) (2007) (163)
Congenital aplasia of the thymus gland (DiGeorge's syndrome). (1968) (156)
Acquired C1-inhibitor deficiency associated with antiidiotypic antibody to monoclonal immunoglobulins. (1985) (156)
A randomized, controlled trial to study the efficacy and safety of C1 inhibitor concentrate in treating hereditary angioedema (1998) (146)
IMPLANTATION OF A FŒTAL THYMUS, RESTORING IMMUNOLOGICAL COMPETENCE IN A PATIENT WITH THYMIC APLASIA (DiGEORGE'S SYNDROME) (1968) (145)
Immunoglobulin Subclasses in Normal Children (1979) (138)
Deficiency of C3 inactivator in man. (1971) (137)
Deficiency of suppressor T cells in the hyperimmunoglobulin E syndrome. (1981) (136)
Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome. (1995) (135)
Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. (1970) (134)
Hereditary angioneurotic edema: a clinical survey. (1966) (134)
Abnormalities of T cell maturation and regulation in human beings with immunodeficiency disorders. (1981) (132)
Primary immunodeficiency diseases: an update (2003) (130)
Hereditary deficiency of the second component of complement (C'2) in man. (1966) (128)
Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema. (1983) (124)
Permeability-increasing activity in hereditary angioneurotic edema plasma. II. Mechanism of formation and partial characterization. (1969) (123)
The primary immunodeficiencies: (second of two parts) (1984) (123)
Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infection. (1970) (121)
Identification and characterization of subpopulations of lymphocytes in human peripheral blood after fractionation on discontinuous gradients of albumin. The cellular defect in X-linked agammaglobulinemia. (1973) (118)
Increased susceptibility to endotoxin shock in complement C3- and C4-deficient mice is corrected by C1 inhibitor replacement. (1997) (110)
Immunology of human immunodeficiency virus infection and the acquired immunodeficiency syndrome. An update. (1987) (109)
Immunodeficiency associated with loss of T4+ inducer T-cell function. (1981) (108)
The Beta1c Globulin in Childhood Nephrotic Syndrome (1965) (106)
Classification of primary immunodeficiencies. (1973) (106)
Biosynthesis of the third component of complement (C3) in vitro by monocytes from both normal and homozygous C3-deficient humans. (1977) (105)
Observations on a Pro-esterase Associated with Partially Purified First Component of Human Complement (C'1).∗ (1956) (104)
Congenital Cardiovascular Disease and Anomalies of the Third and Fourth Pharyngeal Pouch (1972) (104)
INTERACTION OF HUMAN THYMUS-DERIVED AND NON-THYMUS-DERIVED LYMPHOCYTES IN VITRO (1973) (103)
Complement deficiencies. (1992) (103)
Increased susceptibility to infection in a patient with type II essential hypercatabolism of C3. (1973) (102)
Gross and ultrastructural observations on lesions produced by intradermal injection of human C3a in man. (1970) (101)
ASSOCIATION OF "NATURAL" ANTIBODIES TO GRAM-NEGATIVE BACTERIA WITH THE γ1-MACROGLOBULINS (1963) (101)
The primary immunodeficiencies. (1971) (96)
Deficiency of T helper cells in transient hypogammaglobulinemia of infancy. (1981) (94)
Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11. (1986) (94)
The gamma globulins. IV. Therapeutic uses of gamma globulin. (1966) (91)
Prolonged infusion of dexmedetomidine for sedation following tracheal resection (2005) (89)
Obstructive Supraglottic Schwannoma: A Case Report and Review of the Literature (2002) (88)
The opsonic fragment of the third component of human complement (C3) (1975) (87)
Polymerase activity in lymphocyte culture supernatants from patients with Kawasaki disease (1986) (87)
Cellular reactivity to Candida albicans antigen. (1966) (86)
Bone marrow transplantation only partially restores purine metabolites to normal in adenosine deaminase-deficient patients. (1981) (86)
Primary immunodeficiency diseases. Report prepared for the WHO by a scientific group on immunodeficiency. (1983) (86)
Heterogeneity of nephritic factor and its identification as an immunoglobulin. (1977) (85)
Hyper immunoglobulin M immunodeficiency. (Dysgammaglobulinemia). Presence of immunoglobulin M-secreting plasmacytoid cells in peripheral blood and failure of immunoglobulin M-immunoglobulin G switch in B-cell differentiation. (1979) (84)
SERUM-DEPENDENT PHAGOCYTOSIS OF PARAFFIN OIL EMULSIFIED WITH BACTERIAL LIPOPOLYSACCHARIDE (1973) (83)
A specific circulating antigen in hamsters infected with Schistosoma mansoni. Detection of antigen in serum and urine, and correlation between antigenic concentration and worm burden. (1969) (82)
Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysis. (1976) (80)
DERMATOMYOSITIS AND FOCAL SCLERODERMA. (1963) (80)
Inactivator of the third component of complement as an inhibitor in the properdin pathway. (1972) (79)
Inherited deficiency of the third component of human complement (C'3). (1969) (76)
Effect of C'1 esterase on vascular permeability in man: studies in normal and complement-deficient individuals and in patients with hereditary angioneurotic edema. (1968) (75)
Mechanism of mononuclear cell activation by an anti-CD43 (sialophorin) agonistic antibody. (1989) (74)
Purine nucleoside metabolism in the erythrocytes of patients with adenosine deaminase deficiency and severe combined immunodeficiency. (1976) (74)
Binding of C3b proceeds by a transesterification reaction at the thiolester site (1982) (73)
Genetic aspects of the complement system. (1971) (73)
A natural model of immunologic tolerance. Tolerance to murine C5 is mediated by T cells, and antigen is required to maintain unresponsiveness (1982) (72)
Adenosine deaminase deficiency: frequency and comparative pathology in autosomally recessive severe combined immunodeficiency. (1979) (72)
Immune complexes (1983) (70)
Inactivation of endotoxin by a humoral component. II. Interaction of endotoxin with serum and plasma. (1958) (70)
Deletions in the ligand for CD40 in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1). (1993) (69)
Establishment of immunological competence in a child with congenital thymic aplasia by a graft of fetal thymus. (1970) (69)
Metabolism of gamma globulin fragments in normal and agammaglobulinemic persons. (1968) (67)
Further observations on the Swiss type of agammaglobulinemia (alymphocytosis). The effect of syngeneic bone-marrow cells. (1966) (67)
Hereditary deficiency of the second component of complement (C2) in man: correlation of C2 haemolytic activity with immunochemical measurements of C2 protein. (1970) (66)
ALYMPHOCYTOSIS, AGAMMAGLOBULINÆMIA, HOMOGRAFTS, AND DELAYED HYPERSENSITIVITY: STUDY OF A CASE (1962) (65)
ALYMPHOCYTOSIS, AGAMMAGLOBULINÆMIA, HOMOGRAFTS, AND DELAYED HYPERSENSITIVITY: STUDY OF A CASE (1962) (65)
Primary immunodeficiency diseases. Report of a World Health Organization scientific group. (1986) (65)
Disease mechanism: Unravelling Wiskott–Aldrich syndrome (1996) (65)
Molecular defects in hereditary angioneurotic edema. (1997) (65)
C1 inhibitor hinge region mutations produce dysfunction by different mechanisms (1992) (65)
Signal transduction via leukocyte antigen CD43 (sialophorin). Feedback regulation by protein kinase C. (1990) (64)
Opsonic activity in the newborn: role of properdin. (1973) (64)
Inactivation of Biologically Active (“Endotoxic”) Polysaccharides by Fresh Human Serum (1957) (64)
Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema. (1987) (63)
Increased serum immunoglobulin E levels following allogeneic bone marrow transplantation. (1980) (63)
Angioedema induced by a peptide derived from complement component C2 (1988) (63)
Transient 19S gammaglobulin deficiency in the newborn infant, and its significance. (1963) (63)
Hereditary deficiency of the second component of complement (C'2) in man: further observations on a second kindred. (1967) (62)
Hereditary splenic hypoplasia. (1968) (61)
Adenosine deaminase activity in normal tissues and tissues from a child with severe combined immunodeficiency and adenosine deaminase deficiency. (1978) (61)
Somatic mutation of human immunoglobulin V genes in the X-linked HyperIgM syndrome. (1995) (60)
Early pre-B cells from normal and X-linked agammaglobulinaemia produce Cμ without an attached VH region (1983) (59)
The gamma globulins. 3. The antibody deficiency syndromes. (1966) (59)
Transinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema. (1993) (59)
Identification of a subpopulation of lymphocytes in human peripheral blood cytotoxic to autologous fibroblasts (1976) (59)
Characterization of human antibody to polyribophosphate, the capsular antigen of Hemophilus influenzae, type B. (1973) (58)
Ontogeny of human T and B lymphocytes during stressed and normal gestation: phenotypic analysis of umbilical cord lymphocytes from term and preterm infants. (1985) (58)
Acquired deficiency of the inhibitor of the first component of complement: report of five additional cases with commentary on the syndrome. (1985) (58)
Classification of the primary immune deficiencies: WHO recommendation. (1970) (58)
Implantation of a foetal thymus, restoring immunological competence in a patient with thymic aplasia (Digeorge's syndrome). (1969) (56)
Anatomy and Physiology of the Salivary Glands (2014) (55)
Tranexamic acid: preoperative prophylactic therapy for patients with hereditary angioneurotic edema. (1977) (55)
The metabolism of C1 inhibitor and C1q in patients with acquired C1-inhibitor deficiency. (1986) (55)
Inactivation of endotoxin by a humoral component. III. Role of divalent cation and a dialyzable component. (1958) (55)
Characterization of residual enzyme activity in fibroblasts from patients with adenosine deaminase deficiency and combined immunodeficiency: evidence for a mutant enzyme. (1976) (53)
Dysfunctional C1-inhibitor(At), isolated from a type II hereditary-angio-oedema plasma, contains a P1 'reactive centre' (Arg444----His) mutation. (1988) (53)
Genotype-Proteotype Linkage in the Wiskott-Aldrich Syndrome1 (2005) (53)
Immunodeficiency to the Epstein-Barr virus in the X-linked recessive lymphoproliferative syndrome. (1978) (53)
ESTIMATION OF THE SERUM BETA-1C GLOBULIN CONCENTRATION: ITS RELATION TO THE SERUM HEMOLYTIC COMPLEMENT TITER. (1965) (50)
Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site. (1990) (49)
Biosynthetic defect in monocytes from human beings with genetic deficiency of the second component of complement. (1975) (49)
Acquired C1 inhibitor deficiency as a result of an autoantibody to the reactive center region of C1 inhibitor. (1994) (48)
Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies. (1985) (48)
In vitro lymphocyte response of patients with immunologic deficiency diseases. (1970) (47)
Structural differences between the two human complement C4 isotypes affect the humoral immune response (1992) (47)
The Role of Bruton's Tyrosine Kinase in B‐Cell Development and Function in Mice and Man a (1995) (45)
The "neurotic edema" (hereditary angioedema). (1969) (44)
Safety and efficacy of a monomeric, functionally intact intravenous IgG preparation in patients with primary immunodeficiency syndromes. (1984) (42)
THE INTERACTION BETWEEN HUMAN MONOCYTES AND RED CELLS (1970) (41)
Synthesis of an M component by circulating B lymphocytes in severe combined immunodeficiency. (1974) (41)
Role of the second component of complement (C2) and plasmin in kinin release in hereditary angioneurotic edema (H.A.N.E.) plasma. (1977) (39)
Homozygous C3 deficiency: detection of C3 by radioimmunoassay. (1977) (38)
ACQUIRED DYSGAMMAGLOBULINEMIA: ELEVATION OF THE 19S GAMMA GLOBULIN AND DEFICIENCY OF THE 7S GAMMA GLOBULIN IN A WOMAN WITH CHRONIC PROGRESSIVE BRONCHIECTASIS. (1963) (37)
Identification and Characterization of Subpopulations of Lymphocytes in Human Peripheral Blood after Fractionation on Discontinuous Gradients of Albumin (1973) (37)
THE THYMUS AND OTHER LYMPHOID TISSUES IN CONGENITAL AGAMMAGLOBULINEMIA. II. DELAYED HYPERSENSITIVITY AND HOMOGRAFT SURVIVAL IN A CHILD WITH THYMIC ALYMPHOPLASIA. (1964) (37)
Enzyme defects and immune dysfunction (1978) (36)
RECURRENT BACTERIAL INFECTIONS AND DYSGAMMAGLOBULINEMIA: DEFICIENCY OF 7S GAMMA-GLOBULINS IN THE PRESENCE OF ELEVATED 19S GAMMA-GLOBULINS (1961) (35)
Recurrent infections, episodic lymphopenia and impaired cellular immunity. (1969) (35)
Meeting report of the Second International Workshop on Primary Immunodeficiency Disease in Man held in St. Petersburg, Florida, February, 1973. (1974) (35)
THE SITE OF SYNTHESIS OF THE 19S γ-GLOBULINS IN DYSGAMMAGLOBULINEMIA (1962) (35)
DETECTION OF GENETICALLY DETERMINED HISTOCOMPATIBILITY ANTIGEN DIFFERENCES BETWEEN HL‐A IDENTICAL AND MLC NONREACTIVE SIBLINGS (1976) (34)
The gamma globulins. I. The structure and synthesis of the immunoglobulins. (1966) (34)
Genetics and biosynthesis of complement proteins. (1981) (32)
Beta-1C-Globulin: Metabolism in Glomerulonephritis (1966) (31)
Synthesis of C1 inhibitor in fibroblasts from patients with type I and type II hereditary angioneurotic edema. (1991) (30)
Severe combined immunodeficiency: a pediatric emergency. (1997) (30)
Immunoregulatory T-cell defects. (1983) (30)
Hereditary Thymic Dysplasia: A Graft-Versus-Host Reaction Induced by Bone Marrow Cells with a Partial 4a Series Histoincompatibility (1969) (30)
Bone-marrow transplantation in severe combined immunodeficiency syndrome. (1971) (29)
Capping and adenosine metabolism. Genetic and pharmacologic studies (1980) (29)
THE ETIOLOGY OF HYPOPROTEINEMIA IN A PATIENT WITH CONGENITAL CHYLOUS ASCITES (1962) (29)
Transfer of C3 nephritic factor from mother to fetus. Is C3 nephritic factor IgG? (1977) (29)
The endotoxins of gram-negative bacteria and host resistance. (1961) (28)
Human factor D of the alternative complement pathway. Physicochemical characteristics and N-terminal amino acid sequence. (1979) (28)
Androgen therapy in hereditary angioneurotic edema. (1976) (27)
Immunopathology (1977) (27)
Putative Mechanisms of the Effect of Intravenous γ-Globulin (1993) (27)
Bone marrow-derived lymphoid cell lines from patients with agammaglobulinemia. (1978) (27)
Studies of a hypomorphic variant of human C3. (1971) (26)
Immunodeficiency with defective T-cell response to interleukin 1. (1984) (26)
Canine Pain Syndrome Is a Model for the Study of Kawasaki Disease (2015) (26)
Pernicous anaemia, hypogammaglobulinaemia, and altered lymphocyte reactivity. A family study. (1972) (26)
Deficiencies of C1 inhibitor. (2005) (25)
A bloody business (1999) (25)
Immunologic Amnesia: Study of an 11-Year-Old Girl with Recurrent Severe Infections Associated with Dysgammaglobulinemia, Lymphopenia and Lymphocytotoxic Antibody, Resulting in Loss of Immunologic Memory (1968) (24)
A cluster of mutations within a short triplet repeat in the C1 inhibitor gene. (1994) (24)
Induction of human immunoglobulin synthesis and secretion in somatic cell hybrids of mouse myeloma and human B lymphocytes from patients with agammaglobulinemia (1978) (24)
MITOGENIC FRACTIONS IN HUMAN PERIPHERAL LYMPHOCYTE EXTRACTS. (1964) (23)
Application of bone marrow transplantation in genetic diseases. (1983) (23)
Deficiency of Epstein-Barr virus (EBV) receptors on B lymphocytes from certain patients with common varied agammaglobulinemia. (1980) (22)
The genetic basis of immunoglobulin-class switching. (1994) (21)
The third component of complement: covalent attachment of a radioactive sugar to the labile binding site of C3 via the alternative pathway. (1981) (21)
Histopathological and ultrastructural observations on tissues from patients with hereditary angioneurotic edema. (1971) (21)
IgM-restricted production of immunoglobulin by lymphoid cell lines from patients with immunodeficiency with hyper IgM (dysgammaglobulinemia). (1981) (21)
C1s-induced vascular permeability in C2-deficient guinea pigs. (1986) (21)
Meeting report of the Second International Workshop on Primary Immunodeficiency Diseases in Man. (1974) (21)
Metabolism of properdin in normal subjects and patients with renal disease. (1975) (21)
The lymphocyte and the thymus gland--congenital and hereditary abnormalities. (1968) (20)
Antihelper T cell autoantibody in acquired agammaglobulinemia. (1981) (20)
Undue susceptibility to infection. (1962) (19)
Clinical applications of complement assays. (1975) (19)
ACQUIRED AGAMMAGLOBULINAEMIA IN SIBLINGS. (1965) (19)
The evolution of MHC restrictions in antigen recognition by T cells in a haploidentical bone marrow transplant recipient. (1989) (17)
Major histocompatibility restriction of antigen recognition by T cells in a recipient of haplotype mismatched human bone marrow transplantation. (1983) (17)
Discontinuous density gradient analysis of human bone marrow: presence of alloantigen--responsive, PHA--unresponsive cells in norman bone marrow; absence of B lymphocytes in the bone marrow of patients with X--linked agammaglobulinemia. (1974) (17)
THE BETA-1C GLOBULIN IN CHILDHOOD NEPHROTIC SYNDROME: LABORATORY DIAGNOSIS OF PROGRESSIVE GLOMERULONEPHRITIS. (1965) (17)
Transient hypogammaglobulinemia, elevated immunoglobulin E levels, and food allergy. (1979) (16)
Urticaria, angioedema, and anaphylaxis. (1992) (16)
Macmillan dictionary of immunology. (1989) (16)
Primary immunodeficiency diseases. (1972) (16)
The primary immunodeficiencies (1). (1984) (15)
THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUM (1969) (15)
Reticuloendothelial clearance in cystic fibrosis and other inflammatory lung diseases. (1988) (15)
DANGERS OF VACCINATION IN LYMPHOPENIC INFANTS. (1964) (15)
Tracheal Resection with Primary Anastomosis in Cadavers: The Effects of Releasing Maneuvers and Length of Tracheal Resection on Tension (2003) (15)
Gastrointestinal complications of immunodeficiency syndromes. (2008) (15)
The endotoxins of gram-negative bacteria and host resistance. (1961) (15)
Dysgammaglobulinaemia and recurrent bacterial infection. (1961) (15)
Defects in cell-mediated immunity. (1986) (15)
New concepts of immunodeficiency. (1981) (14)
The primary immunodeficiencies: dermatologic manifestations. (1976) (14)
Auto-immunosuppression: Recurrent infections associated with immunologic unresponsiveness in the presence of an auto-antibody to IgG (1972) (14)
Autoimmunity and immunodeficiency disease. (2007) (14)
The immunology series comes to an end. (2001) (13)
Dictionary of Immunology (1990) (13)
Zoonotic filariasis with lymphedema in an immunodeficient infant. (1984) (13)
Case Studies in Immunology (1996) (13)
Observations on the ultrastructure of lesions induced in human and guinea pig skin by C 1 esterase and polypeptide from hereditary angioneurotic edema (HANE) plasma. (1975) (13)
The Xg Blood Groups and Congenital Hypogammaglobulinemia (1965) (12)
Successful gene therapy for severe combined immunodeficiency. (2002) (12)
Immunological Deficiency Disease (1972) (12)
Restricted classes of immunoglobulin produced by a lymphoid cell line from a patient with agammaglobulinemia. (1978) (12)
The macroglobulins. (1962) (12)
Elsewhere in This Issue... (1979) (11)
Polymerase activity in lymphocyte culture supernatants from patients with Kawasaki disease. (1986) (11)
Lymphoma, immunodeficiency and the Epstein-Barr virus. (1977) (11)
X chromosome linked immunodeficiency. (1990) (11)
Role of complement components in the susceptibility to Plasmodium berghei infection among inbred strains of mice. (1975) (10)
INACTIVATION OF ENDOTOXIN BY A HUMORAL COMPONENT (1958) (10)
Inactivation of endotoxin by a humoral component. VI. Two separate systems required for viable and killed Salmonella typhosa. (1960) (10)
Inherited deficiencies of complement proteins in man (2005) (10)
Complement in the serum and venom of Brazilian snakes (Crotalidae). (1984) (10)
Pathways to the complement system. (1972) (10)
Genetics of complement. (1980) (9)
An outbreak of Ritter's disease. (1961) (9)
Putative mechanisms of the effect of intravenous gamma-globulin. (1993) (9)
The Prevalence of Colonization with Drug-Resistant Pneumococci among Adult Workers in Children's Daycare (2007) (9)
A CHANGE IN HL-A PHENOTYPE ASSOCIATED WITH A SPECIFIC BLOCKING FACTOR IN THE SERUM OF AN INFANT WITH SEVERE COMBINED IMMUNODEFICIENCY DISEASE (1972) (8)
Isolation of poliovirus--John Enders and the Nobel Prize. (2004) (8)
The catabolism of C1(-)-inhibitor and the pathogenesis of hereditary angio-edema. (1984) (8)
Somatic cell hybrids of mouse myeloma cells and B lymphocytes from a patient with agammaglobulinemia: failure to secrete human immunoglobulin. (1979) (8)
Structural characterization of C1-esterase inhibitor (C1̄-INH) and comparison with dysfunctional proteins from individuals with hane (1982) (8)
Genetic defects of complement in man (1978) (8)
Is Factor D of the Alternative Pathway a Fragment of Thrombin? (1978) (7)
INACTIVATION OF ENDOTOXIN BY A HUMORAL COMPONENT (1958) (7)
Hereditary angioneurotic edema and its correction with androgen therapy. (1980) (7)
Kinin generation in hereditary angioneurotic edema (H.A.N.E.) plasma. (1983) (7)
Sickle-cell disease and the properdin system. (1973) (7)
Interactions of plasma kallikrein and C1-s with normal and dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema: analytic gel studies. (1987) (7)
The use of cell separation techniques and isantibody to host antigens in the treatent of severe combined immunodeficiency disease with HL-A incompatible maternal marrow. (1974) (7)
Intravenous Gamma Globulin (2010) (7)
IgG subclass studies of C3 nephritic factor. (1978) (7)
Component of Human Complement (C'3) (1969) (7)
Intravenous dissociated gamma globulin in control of hypogammaglobulinemia. (1969) (6)
Metabolism of radiolabelled complement proteins in health and disease (1984) (6)
Viral Inhibitors of Biological Origin. II. A Viral Inhibitory Factor Obtained from E. coli 0111 and Inhibition of Viral Replication by Nucleic Acid Derivatives.∗ (1964) (6)
Localization of the genetic defect in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1) to the CD40 ligand gene. (1993) (6)
916 IMMUNOREGULATORY ABNORMALITIES IN KAWASAKI DISEASE (1981) (6)
The Primary Immunodeficiencies and Serum Complement Defects (1980) (6)
A point mutation in exon 2 of the CD40 ligand gene causes the simultaneous expression of two defective mRNA species in X-linked hyperimmunoglobulinemia M. (1995) (5)
Programmed for defence (2000) (5)
TRANSIENT 19S GAMMA1-GLOBULIN DEFICIENCY IN THE NEWBORN INFANT, AND ITS SIGNIFICANCE (1963) (5)
Alterations in Membrane Fatty Acid (FA) Turnover in Vitamin E Deficient Erythrocytes (E-RBC) During Exposure to Hydrogen Peroxide (1970) (5)
Diagnosis and treatment of antibody deficiency syndromes. (1968) (5)
Studies with intravenous gamma globulin. (1967) (5)
Inhibition of C1s-induced vascular leakage in guinea pigs by substituted benzamidine and pyridinium compounds. (1977) (5)
IMMUNOLOGICAL COMPETENCE OF THE NEWBORN INFANT. (1964) (5)
Hereditary Deficiency oftheSecond Component of Complement (C2)inMan:Correlation ofC2 Haemolytic Activity withImmunochemical Measurements ofC2Protein (1970) (5)
Attempted immunologic reconstitution of patients with combined immune deficiency syndrome with bone marrow transplantation from histoincompatible donors. (1975) (5)
Alymphocytosis, agammaglobulinaemia, homografts, and delayed hypersen sitivity: study of a case. (1962) (5)
Macrophage migration inhibition test. (1970) (5)
Genetic defects of the complement system. (1991) (5)
Interactions of plasma kallikrein and C1-s with normal and dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema: analytic gel studies (1987) (5)
Recent Advances in Primary and Acquired Immunodeficiencies (1986) (5)
Abstracts of Papers Presented at the Third International Complement Workshop, Harvard Medical School, Boston, Massachusetts, June 3–5, 1968 Genetic Aspects of Human C′3 (1968) (5)
Human inhibitor of the first component of complement , Cl : Characterization of cDNA clones and localization of the gene to chromosome 11 ( protease inhibitors / serpins ) (4)
TITLE: Surgery for Exophthalmos SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2004) (4)
The primary immunodeficiencies. (2). (1984) (4)
Toxic hazards: parathion. (1960) (4)
The gamma globulins. I. The structure and synthesis of the immunoglobulins. (1966) (4)
CASE 1 Congenital Asplenia : The role of the spleen in immunity. (2010) (4)
John F. Enders (1897–1985) (1985) (4)
Transplantation in severe combined immunodeficiency disease with hl-a identical bone marrow. (1975) (4)
Pernicious treatment (1993) (4)
The complement system and increased susceptibility to infection. (1971) (4)
Aid on AIDS (1988) (4)
Restoration by Purified C 3 b Inactivator of Complement-Mediated Function In Vivo in a Patient with C 3 b Inactivator Deficiency (4)
Ultrastructure of Circulating Lymphocytes in Thymus Disorders (1971) (4)
Immunoelectrophoretic Examination of Agammaglobulinæmia (1961) (3)
Beta-1C-Globulin in Glomerular Nephritis (1966) (3)
Further Studies of Homozygous C3 Deficiency (1976) (3)
726 CONTROL OF HUMAN MONOCYTE FUNCTION BY Fc FRAGMENTS OF IgG (1978) (3)
Immunology of leishmaniasis. (1993) (3)
Rapid Publication Transinhibition of C 1 Inhibitor Synthesis in Type I Hereditary Angioneurotic Edema (2013) (3)
Immune abnormalities in patients lacking a lymphocyte surface glycoprotein. (1984) (3)
Prognostic value of antibody-dependent assays for presensitization in bone marrow transplant recipients. (1978) (3)
Genetic deficiencies in specific immune responses. (1990) (3)
[Classification of primary immune deficiencies]. (1971) (2)
Gell and Coombs for the nineteen eighties (1982) (2)
PHYSICOCHEMICAL CHARACTERIZATION OF NATURALLY OCCURRING ANTIBODIES TO GRAM- NEGATIVE BACTERIA. (1967) (2)
679 KINETIC ANALYSIS OF SOLID PHASE C3 FRAGMENTS DEPOSITED ON CROSS-LINKED DEXTRAN GEL BEADS (1978) (2)
Genetic Deficiencies of the Complement System (1985) (2)
IMMOBILIZATION HYPERCALCEMIA AFTER SINGLE LIMB FRACTURES IN CHILDREN & ADOLESCENTS (1977) (2)
Lymphoid cell lines from patients with "non-secretory" agammaglobulinemia produce glycosylated heavy chains which are reduced in molecular weight. (1984) (2)
Solubilization of C3 fragments deposited on cross-linked dextran gel beads. (1979) (2)
Lymphocytotoxins and immunologic unresponsiveness. (1975) (2)
GPL-115 deficiency: a new class of immunodeficiencies. (1983) (2)
Successful bone marrow transplantation in sensitized recipients. (1979) (2)
41. The B cell defect in hyper IgM immunodeficiency (dysgammaglobulinemia) (1978) (2)
Complement: ontogeny and phylogeny. (1974) (2)
Assessment of the B-lymphocyte population in agammaglobulinemia. (1975) (2)
The end of history (1996) (2)
Genetic Defects Affecting C3 Associated with Increased Susceptibility to Infections (1973) (2)
Complement and immunologic disease. (1977) (2)
Defective expression of the CD 40 ligand in X chromosome-linked immunoglobulin deficiency with normal or elevated IgM ( isotype switching / immunodeflciency / switch recombination ) (2005) (2)
Clinical aspects of immunology. Volume 3. (1993) (1)
Primary immunodeficiency diseases : proceedings of the Workshop on Primary Immunodeficiency Diseases, held in Gmunden, Austria, on 19-21 August 1985 (1986) (1)
Complement and Disease States (1971) (1)
Research with clinical detachment (1985) (1)
Brazilian Snake Serum and Venom: Studies of the Alternative Pathway and C3 in Man and Serpent (1978) (1)
3-HYDROXY-3 METHYL GLUTARYL COENZYME A (HMG COA) REDUCTASE ACTIVITY IN FIBROBLASTS FROM PHENOTYPIC HOMOZYGOUS TYPE II HY-PERLIPOPROTEINEMIA (HHLPII) (1974) (1)
Defects in Immunological Development in Man (2008) (1)
Complex defences (1988) (1)
linked Severe Combined Immunodeficiency (2010) (1)
Structural Differences between the Two Human Complement C 4 Isotypes Affect the Humoral Lmmune Response (2003) (1)
IgG Subclass Studies of C3 Nephritic Factor (C3NeF) (1978) (1)
B-cell diseases (1993) (1)
Attachment of [35S]cysteine to the labile site of the third component of complement via the alternative pathway. (1983) (1)
Deficiencies of Cl inhibitor (2005) (1)
62 Hereditary Splenic Hypoplasia (1967) (1)
Case Studies in Immunology: Toxic Shock Syndrome : A Clinical Companion (2010) (1)
The acquired immunodeficiency syndrome (AIDS). (1985) (1)
The immunology of helminth infections. (1993) (1)
Synthesis of C 1 Inhibitor in Fibroblasts from Patients with Type I and Type 11 Hereditary Angioneurotic Edema (1)
Disorders of the complement and properdin systems. (1972) (1)
Charles A. Janeway. (1994) (1)
915 DEFICIENCY OF HELPER T CELLS IN TRANSIENT HYPOGAMMA-GLOBULINEMIA (1981) (1)
Introduction: Immunomodulation: Role of Intravenous Immunoglobulins (1989) (1)
Overview: parasitism and immunity. (1993) (1)
REVERSE TRANSCRIPTASE ACTIVITY (RTA) IN PERIPHERAL BLOOD MONONUCLEAR CELL (PBMC) CULTURES (CXS) FROM PATIENTS (PTS) WITH KAWASAKI DISEASE (KD) (1987) (1)
CASE 26 Toxic Shock Syndrome : Superantigens cause excessive stimulation of T cells and macrophages. (2010) (1)
First description of an acquired immunodeficiency. (1988) (1)
T cell : B cell collaboration--the response to polysaccharide antigens. (1989) (1)
Place for overall immunity (1987) (1)
Posttransplantation lymphoproliferative disorder of the paranasal sinuses in a child (2006) (1)
Brazen anatomy (1992) (1)
Keeping Abreast of Immunology (1981) (1)
Case Studies in Immunology: Lepromatous Leprosy : A Clinical Companion (2010) (1)
Case Studies in Immunology: X-linked Lymphoproliferative Syndrome : A Clinical Companion (2010) (0)
CASE 20 T-Cell Lymphoma : A malignancy of functional T lymphocytes. (2010) (0)
Case Studies in Immunology: Multiple Myeloma : A Clinical Companion (2011) (0)
Defects in complement C3 receptor-coupled functions with normal C3b receptor density and affinity in human neutrophils that lack a surface membrane glycoprotein (GP15o) (1982) (0)
Case Studies in Immunology: Factor I Deficiency : A Clinical Companion (2010) (0)
Case Studies in Immunology: X-linked Agammaglobulinemia : A Clinical Companion (2010) (0)
Acquired agammaglobulinemia with circulating b cells detection of discrete defects using il 4 dependent ige isotype switching (1992) (0)
Book ReviewA History of Immunology (1990) (0)
, MD DATE : Wednesday , January 24 , 2001 (2014) (0)
, MD ARCHIVIST : (2014) (0)
Case Studies in Immunology: A Kidney Graft for Complications of Autoimmune Insulin-Dependent Diabetes Mellitus : A Clinical Companion (2010) (0)
Case Studies in Immunology: Myasthenia Gravis : A Clinical Companion (2010) (0)
Case Studies in Immunology: Hemolytic Disease of the Newborn : A Clinical Companion (2010) (0)
Human graft versus host disease. (1980) (0)
Case Studies in Immunology: Interferon-γ Receptor Deficiency : A Clinical Companion (2010) (0)
Case Studies in Immunology: Congenital Asplenia : A Clinical Companion (2010) (0)
The specific notion (1996) (0)
Microdebrider excision of a lipoma of the esophageal inlet. (2003) (0)
CASE 4 Hereditary Angioneurotic Edema : Regulation of complement activation. (2010) (0)
CASE 46 A Kidney Graft for Complications of Autoimmune Insulin-Dependent Diabetes Mellitus : Mechanisms of graft rejection and HLA associations (2010) (0)
Case Studies in Immunology: Acute Systemic Anaphylaxis : A Clinical Companion (2010) (0)
Case Studies in Immunology: Leukocyte Adhesion Deficiency : A Clinical Companion (2010) (0)
The immunology of African trypanosomiasis. (1993) (0)
Book ReviewClinical Immunology (1981) (0)
Case Studies in Immunology: Pemphigus Vulgaris : A Clinical Companion (2010) (0)
CASE 9 X-linked Hypohydrotic Ectodermal Dysplasia and Immunodeficiency : Immunodeficiency due to a defective component in an intracellular signaling pathway required for both innate and adaptive immunity. (2010) (0)
Canine pain syndrome: A model for Kawasaki disease (1992) (0)
Journey of a discovery (2001) (0)
Allergy, immunology, and related disorders (1990) (0)
Case Studies in Immunology: Rheumatoid Arthritis : A Clinical Companion (2010) (0)
Case Studies in Immunology: Chronic Granulomatous Disease : A Clinical Companion (2010) (0)
CASE 45 Hemolytic Disease of the Newborn : The adaptive immune response distinguishes different individuals within a species. (2010) (0)
Pernicious anemia, concordant twins, and immune dysfunction (1971) (0)
107 The metabolism of C1 inhibitor and C1q in acquired C1 inhibitor deficiency (1985) (0)
Case Studies in Immunology: Drug-Induced Serum Sickness : A Clinical Companion (2010) (0)
From fantasy to fact (1983) (0)
TITLE: Rhinosinusitis: Current Concepts SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2002) (0)
Book ReviewImmunological Diseases. (1966) (0)
Isotypes of surface immunoglobulin on B lymphocytes from patients with immune deficiency (2004) (0)
CASE 37 Contact Sensitivity to Poison Ivy : A delayed hypersensitivity reaction to a hapten. (2010) (0)
Case Studies in Immunology: Common Variable Immunodeficiency : A Clinical Companion (2010) (0)
The gamma globulins. 3. The antibody deficiency syndromes. (1966) (0)
CASE 23 X-linked Lymphoproliferative Syndrome : A defect in the immune response to a virus. (2010) (0)
MONOCYTES FROM PATIENTS WITH GENETIC DEFICIENCY OF THE THIRD COMPONENT OF COMPLEMENT (C3) PRODUCE C3 IN VITRO (1977) (0)
CASE 16 Omenn Syndrome : A defect in V(D)J recombination results in severe immunodeficiency. (2010) (0)
Primary immunodeficiency. (1974) (0)
Defence work (1989) (0)
CASE 2 Chronic Granulomatous Disease : A specific failure of phagocytes to produce H and superoxide. (2010) (0)
Case Studies in Immunology: X-linked Severe Combined Immunodeficiency : A Clinical Companion (2010) (0)
Lupus Erythematosus. A Review of the Current Status of Discoid and Systemic Lupus Erythematosus and their Variants (1966) (0)
Case Studies in Immunology: Autoimmune Lymphoproliferative Syndrome (ALPS) : A Clinical Companion (2010) (0)
CASE 40 Myasthenia Gravis : The immune response turns against the host. (2010) (0)
Case Studies in Immunology: Deficiency of the C8 Complement Component : A Clinical Companion (2010) (0)
TITLE: Stridor, Aspiration, and Cough in Children SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2003) (0)
CASE 43 Systemic Lupus Erythematosus : A disease caused by immune complexes. (2010) (0)
TITLE: Recurrent Respiratory Papillomatosis SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2003) (0)
"Elsewhere in this issue..." [ediotiral]. (1979) (0)
Successful bone marrow transplantation in sensitized recipients. [Effect of in vitro irradiation on cytotoxicity of bone marrow cells] (1979) (0)
Case Studies in Immunology: Multiple Sclerosis : A Clinical Companion (2012) (0)
INACTIVATION OF E N D O T O X I N BY A HUMORAL COMPONENT II I . ROLE OF DIVALENT CATION AND A DIALYZ~LV. Com'ONV~vr BY FRED (2003) (0)
Genetic deficiencies of the complement system: an overview (1993) (0)
Case Studies in Immunology: : X-linked Hyper IgM Syndrome : A Clinical Companion (2010) (0)
CASE 31 Acquired Immune Deficiency Syndrome (AIDS) : Infection can suppress adaptive immunity. (2010) (0)
The role of serum factors in the enhancement of phagocytosis. (1969) (0)
Case Studies in Immunology: Autoimmune Hemolytic Anemia : A Clinical Companion (2010) (0)
Molecular and cellular mechanisms in disease. vols. 1 and 2: by Julien L. Van Lancker, published by Springer-Verlag, Berlin, 1976. DM362.− ($148.50) (xx + 1168 pages) (1977) (0)
Immunodeficieny with Normal or Increased Immunoglobulin M (1994) (0)
Case Studies in Immunology: Interleukin 1 Receptor-associated Kinase 4 Deficiency : A Clinical Companion (2010) (0)
THE NATURE OF AUTOIMMUNE-DISEASE - GENERAL DISCUSSION (1987) (0)
CASE 22 Wiskott–Aldrich Syndrome : Role of the actin cytoskeleton in T-cell function. (2010) (0)
Reply To Matzdorff, Kemkes‐Matthes And Pralle (2000) (0)
672 Pharmacokinetic evaluation of a vapor-heated C1-inhibitor concentrate (2000) (0)
The gamma globulin content of meconium and amniotic fluid and the intestinal immunity of the newborn to poliovirus (2005) (0)
Genetic and Pharmacologic Studies (1980) (0)
Congenital Asplenia : The role of the spleen in immunity. (2010) (0)
Case Studies in Immunology: Omenn Syndrome : A Clinical Companion (2010) (0)
747 A NATURALLY OCCURRING INHIBITOR OF LYMPHOCYTE FUNCTION FROM A CUTANEOUS LYMPHOMA (1978) (0)
Book reviewBasic immunogenetics: By H. H. Fudenberg, J. R. L. Pink, D. P. Stites, and A. -C. Wang. Oxford University Press, New York, 1972. 212 pp. $7.95 clothbound, $5.50 paperback (1973) (0)
1 TITLE : Nonneoplastic Diseases of the Salivary Glands SOURCE : Grand Rounds Presentation (2014) (0)
Case Studies in Immunology: Systemic Lupus Erythematosus : A Clinical Companion (2010) (0)
Mouse thymocyte-fibroblast hybrid cells, retention of thymic function and loss of theta antigen. Abstr. (1973) (0)
Case Studies in Immunology: Wiskott-Aldrich Syndrome : A Clinical Companion (2010) (0)
γ-Globulin replacement therapy in immunodeficiency (1987) (0)
Case Studies in Immunology: T-Cell Lymphoma : A Clinical Companion (2010) (0)
Case Studies in Immunology: X-linked Hypohydrotic Ectodermal Dysplasia and Immunodeficiency : A Clinical Companion (2010) (0)
The macroglobulins. (1962) (0)
Ontogeny of Immunity, edited by R. T. Smith, M.D., R. A. Good, M.D., and P. A. Miescher, M.D. Gainesville, Florida: University of Florida Press, 1967, 208 pp. $15.00 (1968) (0)
Case Studies in Immunology: Adenosine Deaminase Deficiency : A Clinical Companion (2010) (0)
TITLE: Conservation Laryngeal Surgery SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2003) (0)
Undiplomatic immunity (1998) (0)
Talk of Kyoto (1985) (0)
Ataxia telangiectasia associated with the hyper-IgM syndrome (1994) (0)
1522 A SUBPOPULATION OF LYMPHOCYTES IN HUMAN PERIPHERAL BLOOD quadruplicate with two fibroblast l ines as targets (2003) (0)
Case Studies in Immunology: Hereditary Periodic Fever Syndromes: A Clinical Companion (2010) (0)
Hereditary C′2 deficiency in man (1966) (0)
Case Studies in Immunology: Acute Infectious Mononucleosis : A Clinical Companion (2010) (0)
CASE 42 Rheumatoid Arthritis : A common, severe inflammatory disease of unknown cause. (2010) (0)
The iC globulin in childhood nephrotic syndrome: The laboratory diagnosis of subacute glomerulonephritis (1965) (0)
Amino acid sequence of human plasma galactoglycoprotein : Identity with the extracellular region of CD 43 ( sialophorin ) ( glycans ) (0)
Case Studies in Immunology: Graft-Versus-Host Disease: A Clinical Companion (2010) (0)
Gamma-globulin replacement therapy in immunodeficiency. (1987) (0)
Immunology of amoebiasis and giardiasis. (1993) (0)
Book Review Edwin J. Cohn and the Development of Protein Chemisty By Douglas M. Surgenor. 434 pp., illustrated. Boston, Center for Blood Research, 2002. (Distributed by Harvard University Press, Cambridge, Mass.) $34.95. 0-674-00962-2 (2003) (0)
Case Studies in Immunology: Activation-induced Cytidine Deaminase (AID) Deficiency : A Clinical Companion (2010) (0)
Case Studies in Immunology: MHC Class II Deficiency : A Clinical Companion (2010) (0)
TITLE: Flaps in Facial Reconstruction SOURCE: Grand Rounds Presentation, UTMB, Dept. of Otolaryngology (2003) (0)
Case Studies in Immunology: Mixed Essential Cryoglobulinemia : A Clinical Companion (2010) (0)
INACTIVATION OF E N D O T O X I N BY A HUMORAL COMPONENT* II . INTERACTION OF ENDOTOXIN WITH SERUM (2003) (0)
Immunology for the Practicing Physician, Jon R. Schmidtke, Ronald M. Ferguson (Eds.). Plenum Press, New York and London (1977) (1978) (0)
Primary immunodeficiency diseases : international workshop held September 12-15, 1982, at Rosario Resort, Orcas Island, Washington, U.S.A. (1983) (0)
CASE 27 Acute Infectious Mononucleosis : Cytotoxic T cells terminate viral infection. (2010) (0)
ISOLATION OF HUMAN LYMPHOCYTE MITOGENIC FACTOR (1977) (0)
CASE 13 Common Variable Immunodeficiency : A failure to produce antibodies against particular antigens. (2010) (0)
CASE 5 Factor I Deficiency : The alternative pathway of complement activation is important in innate immunity. (2010) (0)
May teach you more of man (1984) (0)
725 SUCCESSFUL CORRECTION OF A BONE MARROW STEM CELL DEFECT (WISKOTT-ALDRICH SYNDROME) BY ALLOGENEIC MARROW TRANSPLANTATION (1978) (0)
Immunoelectrophoretic examination of agammaglobulinaemia. (1961) (0)
Transforming the theatre of surgery (1997) (0)
Case Studies in Immunology: Immune Dysregulation, Polyendocrinopathy, Enteropathy X-linked Disease : A Clinical Companion (2010) (0)
CASE 47 Graft-Versus-Host Disease : Alien T cells react against their new host. (2010) (0)
CASE 28 Mixed Essential Cryoglobulinemia : Chronic infection can lead to immune-complex disease. (2010) (0)
X-linked immunodeficiency: B-cell diseases. (1993) (0)
Phylogeny of Immunity, edited by R. T. Smith, M.D., P. A. Miescher, M.D., and R. A. Good, M.D. Gainesville, Florida: University of Florida Press, 1966, 276 pp. $15.00 (1968) (0)
Thorny controversies (1992) (0)
CASE 14 X-linked Severe Combined Immunodeficiency : The maturation of T lymphocytes. (2010) (0)
CASE 34 Atopic Dermatitis : Skin as a target organ for allergy. (2010) (0)
Immunity Deficiency in Children (1972) (0)
Fc RECEPTOR MEDIATED CLEARANCE, IN VIVO, IN PATIENTS WITH RECURRENT PULMONARY INFECTIONS (1987) (0)

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