William Krivit

Q: What Schools Are Affiliated With William Krivit

William Krivit is affiliated with the following schools: Tokai University, University of Minnesota

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Philosophy
Biology

William Krivit's Degrees

Doctorate Medicine Harvard University
PhD Immunology Stanford University

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William Krivit'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

Virus‐associated hemophagocytic syndrome A benign histiocytic proliferation distinct from malignant histiocytosis (1979) (1015)
Transplantation of unrelated donor umbilical cord blood in 102 patients with malignant and nonmalignant diseases: influence of CD34 cell dose and HLA disparity on treatment-related mortality and survival. (2002) (1009)
Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder. (1969) (683)
Allogeneic mesenchymal stem cell infusion for treatment of metachromatic leukodystrophy (MLD) and Hurler syndrome (MPS-IH) (2002) (673)
Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease. (2005) (532)
Cord-blood transplants from unrelated donors in patients with Hurler's syndrome. (2004) (465)
Successful bone-marrow transplantation for infantile malignant osteopetrosis. (1980) (446)
Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity. (1968) (403)
Overwhelming postsplenectomy infection (1979) (330)
Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group. (1998) (329)
Cerebral X-linked adrenoleukodystrophy: the international hematopoietic cell transplantation experience from 1982 to 1999. (2004) (327)
Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndrome. (1996) (321)
Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy (2000) (277)
Adrenoleukodystrophy: a scoring method for brain MR observations. (1994) (277)
Simultaneous occurrence of mongolism and leukemia; report of a nationwide survey. (1957) (259)
Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III. (1999) (254)
A randomized study of the prevention of acute graft-versus-host disease. (1982) (238)
Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases. (1999) (234)
The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979). (1980) (225)
Neuropsychological outcomes of several storage diseases with and without bone marrow transplantation (1995) (194)
Hematopoietic stem-cell transplantation in globoid-cell leukodystrophy. (1998) (190)
Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Biochemical and clinical status 24 months after transplantation. (1984) (183)
Male Donor‐derived Cells in the Brains of Female Sex‐mismatched Bone Marrow Transplant Recipients: A Y‐Chromosome Specific In situ Hybridization Study (1993) (179)
Acute and chronic effects of methotrexate on hepatic, pulmonary, and skeletal systems (1976) (175)
Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases (2004) (169)
Overwhelming sepsis following splenectomy for trauma. (1976) (167)
Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases. (1995) (142)
Unrelated donor bone marrow transplantation: influence of HLA A and B incompatibility on outcome. (1995) (137)
Busulfan disposition in children. (1990) (135)
Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantation. (1990) (132)
Bone marrow transplantation for globoid cell leukodystrophy, adrenoleukodystrophy, metachromatic leukodystrophy, and Hurler syndrome. (1999) (127)
Thrombotic and hemorrhagic strokes complicating early therapy for childhood acute lymphoblastic leukemia (1980) (116)
TRANSIENT CONGENITAL LEUKEMIA IN 7 INFANTS WITH MONGOLISM. (1964) (112)
Impaired Cellular Resistance to Herpes-Simplex Virus in Wiskott-Aldrich Syndrome (1965) (111)
Late-onset Krabbe disease (globoid cell leukodystrophy): clinical and biochemical features of 15 cases. (1991) (110)
The effect of L-asparaginase on antithrombin, plasminogen, and plasma coagulation during therapy for acute lymphoblastic leukemia. (1982) (105)
The occurrence of leukemia in patients with the Shwachman syndrome. (1981) (104)
Children with mucopolysaccharidosis: perioperative care, morbidity, mortality, and new findings. (1993) (101)
Globoid cell leukodystrophy: distinguishing early-onset from late-onset disease using a brain MR imaging scoring method. (1999) (99)
Intensive therapy followed by bone marrow transplantation for patients with acute lymphocytic leukemia in second or subsequent remission: determination of prognostic factors (a report from the University of Minnesota Bone Marrow Transplantation Team). (1983) (98)
Adrenoleukodystrophy: Phenotypic variability and implications for therapy (1992) (94)
Usefulness of bone marrow transplantation in the Hurler syndrome. (2003) (94)
Single versus multiple dose dactinomycin therapy of Wilms's tumor. A controlled co-operative study conducted by the Children's Cancer Study Group A (formerly Acute Leukemia Co-operative Chemotherapy Group A). (1968) (91)
Hematopoietic cell therapy for metabolic disease. (2007) (89)
The future for treatment by bone marrow transplantation for adrenoleukodystrophy, metachromatic leukodystrophy, globoid cell leukodystrophy and Hurler syndrome (1995) (86)
Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy. (1996) (85)
Aldrich's syndrome (thrombocytopenia, eczema, and infection infants); studies of the defense mechanisms. (1959) (85)
The development of malignancy in the course of the Aldrich syndrome. (1966) (84)
Relief of pain of Fabry's disease by diphenylhydantoin (1973) (82)
Phase II study of VP-16-213 in childhood malignant disease: a Children's Cancer Study Group Report. (1979) (81)
Wolman disease successfully treated by bone marrow transplantation (2000) (80)
Intraocular retinoblastoma group V: an analysis of prognostic factors. (1985) (77)
Ocular abnormalities in the mucopolysaccharidoses after bone marrow transplantation. Longer follow-up. (1998) (76)
Eosinophilic leukemia: Report of a case, with review and classification (1961) (76)
Allogeneic bone marrow transplantation in acute nonlymphocytic leukemia: a pilot study. (1982) (74)
The effect of L‐asparaginase on plasma coagulation factors in acute lymphoblastic leukemia (1977) (73)
Late-onset metachromatic leukodystrophy (2006) (73)
Plasma concentrations of 4-hydroxycyclophosphamide and phosphoramide mustard in patients repeatedly given high doses of cyclophosphamide in preparation for bone marrow transplantation. (1984) (72)
Microglia: The Effector Cell for Reconstitution of the Central Nervous System following Bone Marrow Transplantation for Lysosomal and Peroxisomal Storage Diseases (1995) (68)
Fatal veno-occlusive disease of the liver following high dose chemotherapy, irradiation and bone marrow transplantation. (1980) (66)
Characteristics of the dementia in late‐onset metachromatic leukodystrophy (1994) (66)
Total lymphoid irradiation and cyclophosphamide as preparation for bone marrow transplantation in severe aplastic anemia (1980) (66)
The simultaneous occurrence of leukemia and mongolism; report of four cases. (1956) (65)
Primary and Secondary Bile Acids in Meconium (1971) (64)
The overwhelming postsplenectomy sepsis problem (1980) (64)
Natural history of primary autoimmune neutropenia in infancy. (1987) (63)
A penicillin-resistant pneumococcus. (1978) (63)
Long-term Outcomes of Adaptive Functions for Children with Mucopolysaccharidosis I (Hurler Syndrome) Treated with Hematopoietic Stem Cell Transplantation (2006) (63)
Bone marrow transplantation for Hurler syndrome: assessment of metabolic correction. (1986) (62)
Phase II trail cisplatin in refractory childhood cancer: Children's Cancer Study Group Report. (1981) (62)
Childhood cerebral form of adrenoleukodystrophy: short-term effect of bone marrow transplantation on brain MR observations. (1994) (62)
Correction of odontoid dysplasia following bone-marrow transplantation and engraftment (in Hurler syndrome MPS 1H) (2000) (61)
Platelet Storage Pool Deficiency and Prostaglandin Synthesis in Chronic Granulocytic Leukaemia (1978) (60)
Comparison of two total body irradiation regimens in allogeneic bone marrow transplantation for acute non-lymphoblastic leukemia in first remission. (1990) (58)
Prognostic significance of surface marker analysis in childhood non‐hodgkin's lymphoproliferative malignancies (1976) (58)
Ocular changes in the mucopolysaccharidoses after bone marrow transplantation. A preliminary report. (1989) (58)
Stem cell bone marrow transplantation in patients with metabolic storage diseases. (2002) (58)
Total lymphoid irradiation and cyclophosphamide conditioning prior to bone marrow transplantation for patients with severe aplastic anemia. (1983) (57)
A comparison of methods for detecting leukocyte antibodies in autoimmune neutropenia (1981) (56)
Bone marrow transplantation for acute nonlymphocytic leukemia in first remission: analysis of prognostic factors. (1985) (56)
Phase II trial of a complex polyriboinosinic-polyribocytidylic acid with poly-L-lysine and carboxymethyl cellulose in the treatment of children with acute leukemia and neuroblastoma: a report from the Children's Cancer Study Group. (1985) (56)
'Pseudolymphoma'. A case associated with primary immunodeficiency disease and polyglandular failure syndrome. (1981) (55)
Effective treatment of α-mannosidosis by allogeneic hematopoietic stem cell transplantation (2004) (54)
Proton MR spectroscopy of childhood adrenoleukodystrophy. (1996) (51)
Relapse rates following cessation of chemotherapy during complete remission of acute lymphocytic leukemia. (1979) (51)
PLasma half-life and urinary excretion of cyclophosphamide in children. (1980) (50)
Neuropsychological development in children with Hurler syndrome following hematopoietic stem cell transplantation. (1998) (49)
Overwhelming infection in children following splenectomy. (1960) (48)
Ceroid accumulation in a patient with progressive neurological disease. (1968) (48)
Vaccine-type pneumococcal pneumonia. Occurrence after vaccination in an asplenic patient. (1979) (46)
Generalized accumulation of neutral glycosphingolipids with GM2 ganglioside accumulation in the brain. Sandhoff's disease (variant of Tay-Sachs disease). (1972) (45)
State of the art review. Bone marrow transplantation treatment for storage diseases. Keystone. January 23, 1992. (1992) (45)
SCLERODERMATOUS GRAFT-VERSUS-HOST DISEASE LIMITED TO AN AREA OF MEASLES EXANTHEM (1978) (45)
PRETRANSPLANT CONDITIONING WITH BUSULFAN (MYLERAN) AND CYCLOPHOSPHAMIDE FOR NONMALIGNANT DISEASES: ASSESSMENT OF ENGRAFTMENT FOLLOWING HISTOCOMPATIBLE ALLOGENEIC BONE MARROW TRANSPLANTATION (1985) (45)
Wolman's disease: a review of treatment with bone marrow transplantation and considerations for the future. (1992) (45)
Analysis of factors affecting development of carpal tunnel syndrome in patients with Hurler syndrome after hematopoietic cell transplantation (2007) (44)
Long-term evaluation of single versus multiple courses of actinomycin D therapy of Wilms's tumor. (1974) (44)
Bone marrow transplantation for non-Hodgkin's lymphoma in children and young adults. A pilot study. (1983) (43)
Hurler syndrome: past, present, and future. (1998) (43)
Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome); an ethical commentary (2000) (43)
Clinical and laboratory evaluation of infants and children with Epstein-Barr virus-induced infectious mononucleosis: report of 32 patients (aged 10-48 months). (1981) (42)
Bone marrow transplantation for genetic diseases. (1987) (42)
Ganciclovir‐resistant cytomegalovirus encephalitis in a bone marrow transplant recipient (2002) (42)
Alpha1-antitrypsin in the respiratory-distress syndrome. (1973) (41)
Continued neurocognitive development and prevention of cardiopulmonary complications after successful BMT for I-cell disease: a long-term follow-up report (2003) (41)
Outcome of second hematopoietic cell transplantation in Hurler syndrome (2002) (41)
Immune thrombocytopenia in severe neonatal infections. (1981) (41)
A phase II study of cisplatin therapy in recurrent childhood brain tumors (1989) (40)
Prevention of deterioration in metachromatic leukodystrophy by bone marrow transplantation. (1987) (40)
Nonspherocytic Haemolytic Anaemia with Increased Red Cell Adenine Nucleotides, Glutathione and Basophilic Stippling and Ribosephosphate Pyrophosphokinase (RPK) Deficiency: Studies on Two New Kindreds (1973) (40)
Total-body irradiation with a high-dose-rate linear accelerator for bone-marrow transplantation in aplastic anemia and neoplastic disease. (1977) (39)
Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the Hurler syndrome. (2001) (39)
Hereditary lymphedema and obstructive jaundice. (1971) (38)
White matter dysfunction and its neuropsychological correlates: a longitudinal study of a case of metachromatic leukodystrophy treated with bone marrow transplant. (1992) (38)
Genu valgum deformity in Hurler syndrome after hematopoietic stem cell transplantation: correction by surgical intervention. (1999) (36)
Defibrination syndrome in an infantborn after abruptio placentae (1968) (36)
Phase II study of cis-dichlorodiammineplatinum(II) in childhood osteosarcoma: Children's Cancer Study Group Report. (1979) (36)
Pathology of the liver in mucopolysaccharidosis: light and electron microscopic assessment before and after bone marrow transplantation. (1992) (36)
Aplastic anemia associated with the Shwachman syndrome. In vivo and in vitro observations. (1981) (35)
Sandhoff’s Disease: Ultrastructural and Biochemical Studies (1972) (35)
Light and electron microscopic features of the liver in mucopolysaccharidosis. (1994) (35)
The need for chemotherapy after prolonged complete remission in acute leukemia of childhood. (1970) (35)
Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome). (2000) (35)
Hematopoietic cell transplantation in fetal lambs with ceroid-lipofuscinosis. (1995) (35)
Hematopoietic dysplasia and marrow hypocellularity in children: a preleukemic condition. (1982) (34)
Resolution of obstructive sleep apnea in Hurler syndrome after bone marrow transplantation. (1988) (34)
Intravascular coagulation in acute stem cell leukemia successfully treated with heparin. (1967) (34)
Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita. (1953) (33)
Proton MR spectroscopy and neuropsychological testing in adrenoleukodystrophy. (1997) (33)
Successful reinduction of patients with acute lymphoblastic leukemia who relapse following bone marrow transplantation. (1987) (33)
Spontaneously acquired factor IX inhibitor in a nonhemophiliac child (1978) (31)
Evaluation of coronary artery disease in the Hurler syndrome by angiography. (1992) (30)
Phase II study of VM-26 in acute leukemia, neuroblastoma, and other refractory childhood malignancies: a report from the Children's Cancer Study Group. (1979) (30)
Induction of remission in acute leukemia of childhood by combination of prednisone and either 6-mercaptopurine or methotrexate. (1966) (30)
WISKOTT-ALDRICH SYNDROME: DETECTION OF CARRIER STATE BY METABOLIC STRESS OF PLATELETS (1978) (30)
Pediatric phase I trial of carboplatin: a Childrens Cancer Study Group report. (1987) (29)
Poor cognitive outcome of eleven children with Sanfilippo syndrome after bone marrow transplantation and successful engraftment (1995) (28)
Cure of three patients who had skeletal metastases in disseminated neuroblastoma. (1968) (27)
Needle biopsy of the liver in infancy and childhood. A safe diagnostic aid in liver disease. (1967) (27)
Longitudinal neurophysiologic studies in a patient with metachromatic leukodystrophy following bone marrow transplantation. (1992) (27)
Identification of nine novel arylsulfatase a (ARSA) gene mutations in patients with metachromatic leukodystrophy (MLD) (2003) (26)
Autonomous production of parathyroid hormone by lymphoblastic leukemia cells in culture. (1979) (26)
Studies of a patient with selective deficiency in absorption of vitamin B12. (1961) (26)
Maintenance therapy in acute leukemia of childhood: Comparison of cyclic vs. sequential methods (1968) (25)
Effective treatment of alpha-mannosidosis by allogeneic hematopoietic stem cell transplantation. (2004) (24)
Fatal arteritis as a complication of Wiskott-Aldrich syndrome. (1979) (24)
Late‐onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G→a mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family (2001) (23)
Impaired lymphocyte transformation in leukemic patients after intensive therapy (1972) (23)
A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome. (1987) (23)
Bone marrow transplantation in metachromatic leukodystrophy. (1986) (23)
Bone marrow transplantation for storage diseases. (1991) (22)
Factor V deficiency in Philadelphia-positive chronic myelogenous leukemia. (1980) (22)
Resection of metastases in Wilms' tumor: a report of three cases cured of pulmonary and hepatic metastases. (1968) (21)
Acute parkinsonian syndrome with demyelinating leukoencephalopathy in bone marrow transplant recipients. (1991) (21)
The effect of L-asparaginase of plasma coagulation factors in acute lymphoblastic leukemia. (1977) (20)
Selective deficiency in collagen-induced platelet aggregation during L-asparaginase therapy. (1980) (20)
Survival in Hurler's disease following bone marrow transplantation in 84 patients (1995) (19)
Total lymphoid irradiation and cyclophosphamide as preparation for bone marrow transplantation in severe aplastic anemia. (1980) (18)
Phase II trial of poly(I,C)-LC, an interferon inducer, in the treatment of children with acute leukemia and neuroblastoma: a report from the Children's Cancer Study Group. (1985) (18)
Oncornavirus-like particles from cultured bone marrow cells preceding leukemia and malignant histiocytosis. (1975) (18)
Oral busulfan pharmacokinetics and engraftment in children with Hurler syndrome and other inherited metabolic storage diseases undergoing hematopoietic cell transplantation (2001) (18)
Benign intracranial hypertension associated with a delayed penicillin reaction. (1969) (17)
CSF findings in adrenoleukodystrophy: correlation between measures of cytokines, IgG production, and disease severity. (1994) (17)
Serial MR after bone marrow transplantation in two patients with metachromatic leukodystrophy. (1994) (17)
Single dose total lymphoid irradiation combined with cyclophosphamide as immunosuppression for human marrow transplantation in aplastic anemia. (1979) (17)
Addition of local radiation after bone marrow remission in acute leukemia in children (1967) (17)
Possible use of CSF glycosphingolipids for the diagnosis and therapeutic monitoring of lysosomal storage diseases (1992) (16)
Comparison of the therapeutic response of patients with childhood acute lymphoblastic leukemia in relapse to vindesine versus vincristine in combination with prednisone and L-asparaginase: a phase III trial. (1981) (16)
Serial study of bone marrow in hemolytic disease of the newborn (erythroblastosis fetalis). (1959) (15)
Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: α-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy) (2000) (15)
Fatal neonatal heptic steatosis: a new familial disorder. (1969) (15)
Renal and hepatic pathology following initial remission of acute leukemia induced by prednisone (1967) (15)
Thrombotic thrombocytopenic purpura. Report of an unusual clinical case and chromium-51 red cell survival studies. (1962) (15)
Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): imaging findings following bone marrow transplantation (1997) (14)
Dense peripheral corneal clouding in Scheie syndrome. (1994) (13)
RETRANSPLANTATION OF HUMAN BONE MARROW: Two IMMUNOSUPPRESSIVE DRUG REGIMENS (1975) (13)
Interferon-alpha n1 in children with recurrent acute lymphocytic leukemia: a phase I study of pharmacokinetics and tolerance. (1988) (13)
A study of the cross-resistance of vincristine and vindesine in reinduction therapy for acute lymphocytic leukemia in relapse. A report for Children's Cancer Study Group. (1980) (13)
A phase II study of diaziquone in children with recurrent or progressive primary brain tumors: A report from the Childrens Cancer Study Group (1990) (13)
Familial leukemia and inherited chromosomal aberration (1977) (13)
Clear cells in the atrioventricular valves of infants with severe human mucopolysaccharidosis (Hurler syndrome) are activated valvular interstitial cells. (2011) (13)
Cerebral X-Linked Adrenoleukodystrophy: The University of Minnesota Hematopoietic Cell Transplantation Experience from 1991 to 2004. (2004) (12)
Methotrexate liver toxicity. (1969) (12)
Defibrination syndrome in an infant born after abruptio placentae. (1968) (12)
Globoid cell leukodystrophy (Krabbe disease): Normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations (2005) (12)
Combination therapy with 6-mercaptopurine (NSC-755) and allopurinol (NSC-1390) during induction and maintenance of remission of acute leukemia in children. (1969) (11)
Paucity of splenic germinal centers: a new and unique splenomegaly syndrome including dysfunctional immune system. (1982) (11)
Congenital nonspherocytic hemolytic anemia; two nonfamilial cases with red cell survival studies. (1956) (11)
Rejection after bone marrow transplantation for aplastic anemia using an identical twin, followed by permanent success utilizing immunosuppression. (1979) (11)
Allogeneic bone marrow transplantation for Niemann-Pick disease (type IA). (1992) (11)
Resting TI‐201 Scintigraphy in the Evaluation of Coronary Artery Disease in Children With Hurler Syndrome (1994) (11)
Combined immunosuppression using cyclophosphamide plus total lymphoid irradiation in preparation for allogeneic marrow transplantation in humans. (1980) (10)
L-asparaginase-induced hypocomplementemia in acute lymphocytic leukemia (ALL) of childhood. (1979) (10)
Type II Hyperlipoproteinemia in Mother and Twins (1969) (10)
Inheritance of a recombinant HL-A haplotype and genetics of the HL-1 region in man (1974) (10)
Improvement of Clinical Expression of Central Nervous System Manifestation in Lysosomal Storage Diseases Treated by Bone Marrow Transplantation (1988) (9)
Anthracycline cardiomyopathy (2005) (9)
Histoplasmosis simulating lymphoma in children. (1979) (9)
Phase II Trial of Indicine N‐Oxide in Relapsed Acute Leukemia of Childhood: A Report from the Childrens Cancer Study Group (1992) (9)
Bis-(N-maleimidomethyl) ether: an antisickling reagent. (1975) (9)
Phase II trial of indicine N-oxide in relapsed pediatric solid tumors (1991) (9)
Bone marrow transplantation for treatment of lysosomal storage diseases : proceedings of a colloquium held May 7, 1985, Washington, D.C. (1986) (9)
Patterns of anti-diuretic function in diabetes insipidus caused by histiocytosis X. (1971) (9)
Evaluation of cyclocytidine in children with advanced acute leukemia and solid tumors. (1979) (8)
Results of a phase i clinical trial of allogeneic mesenchymal stem cell (msc) transplantation in patients with hurlerdisease and metachromaticleukodystrophy (mld) (2000) (8)
A clinical study of an exanthem due to ECHO virus type 9. (1959) (8)
Radiological case of the month. Coarctation of the aorta in Hurler syndrome. (2000) (8)
Localized bone marrow relapse in acute lymphoblastic leukemia. (1979) (7)
Lymphocyte transformation in leukemic serum (1975) (7)
Eosinophilic peritonitis. Report of two cases. (1967) (7)
Cisplatin, vinblastine, and bleomycin (CVB) therapy for relapsed disseminated neuroblastoma. (1984) (7)
Virus-induced histiocytosis with erythrophagocytosis (1980) (6)
Hyperbaric oxygen, whole-body X irradiation, and cyclophosphamide combination therapy in mouse leukemia L1210. (1966) (6)
Detection of platelet associated IgG in immune thrombocytopenia: A new assay employing protein a and peroxidase anti‐peroxidase (PROA‐PAP) (1980) (6)
Combined Cyclophosphamide-Total Lymphoid Irradiation Compared to Other Forms of Immunosuppression for Human Marrow Transplantation (1979) (6)
Chemistry and Metabolism of Glycosphingolipids in Fabry’s Disease (1972) (6)
Transient autoimmune neutropenia due to anti-NA1 antibody. (1980) (5)
Lymphocyte transformation in leukemic serum. (1975) (5)
A follow-up report of long-term survivors of childhood acute lymphoblastic or undifferentiated leukemia. A report for Childrens Cancer Study Group. (1979) (5)
SPONTANEOUSLY ACQUIRED FACTOR IX INHIBITOR IN A NON-HEMOPHILIAC CHILD (1977) (5)
Hereditary adenocarcinoma of the colon in childhood: Association with the cancer family syndrome (1978) (4)
Bone marrow curettage in childhood myelofibrosis. (1975) (4)
Transient myeloid metaplasia associated with an unusual hemoglobin in a newborn infant. (1979) (4)
An initial report of a phase-III trial comparing vindesine and vincristine for acute lymphocytic leukemia of childhood (2004) (4)
A phase II study of diaziquone in children with recurrent or progressive solid tumors. Report from the Childrens Cancer Study Group. (1990) (4)
Low molecular weight glycogen as a cause of generalized glycogen storage disease. (1973) (4)
Bone marrow transplantation in pediatrics. (1983) (4)
Value of Random Urinary Homovanillic Acid and Vanillylmandelic Acid Levels in the Diagnosis and Management of Patients with Neuroblastoma: Comparison with 24-Hour Urine Collections (1985) (3)
Studies of persistent herpes virus infection in children with the Aldrich syndrome. (1962) (3)
Elevated levels of sphingolipids in type II (a+b) hyperlipoproteinemia (1974) (3)
The results of allogeneic bone marrow transplantation (BMT) in patients with acute non-lymphocytic leukemia (ANLL) in first remission: Comparison of two sequential studies utilizing different total body irradiation regimens (1987) (3)
Immunosuppressive therapy for severe aplastic anemia (1980) (3)
Potential toxicity of iron overload in successive generations of rats. (1975) (3)
Correction of inborn errors of metabolism by bone marrow transplant. (1983) (3)
Phase II trial of prednimustine in children with recurrent cancer: a Children's Cancer Study Group report. (1982) (3)
CHYLOTHORAX IN ACUTE LEUKEMIA (1970) (3)
CATALASE ACTIVITY IN MOUSE LEUKEMIA L1210. (1965) (3)
Three Years of Experience With Random Urinary Homovanillic and Vanillylmandelic Acid Levels in the Diagnosis of Neuroblastoma (1987) (2)
Pulmonary Risk Factors in Allogeneic Transplantation for Hurler Syndrome. (2004) (2)
Cord Blood Transplantation for Lysosomal Storage Diseases Demonstrates the Potential of Cord Blood Cells for Future Cellular Therapies. (2004) (2)
A phase II study of diaziquone in childhood leukemia: a report from the Children's Cancer Study Group. (1988) (2)
The liver in noncirrhotic -1-antitrypsin deficiency. (1971) (2)
The worldwide hematopoietic cell transplantation experience for cerebral x-adrenoleukodystrophy (2000) (2)
Familial autoimmune disorders: emphasis on the polyglandular failure syndrome. (1985) (2)
Phase I/II study of bisantrene in childhood cancer: a report from the Childrens Cancer Study Group. (1988) (2)
Vinblastine, procarbazine, and cytosine arabinoside in combination for reinduction of childhood acute myelocytic leukemia. (1976) (2)
Cranial irradiation of young rats impairs later learning and growth (1979) (2)
Complex alpha-thalassemia-like syndrome: a cause of neonatal normoblastemia. (1976) (1)
4'-DEMETHYL-EPIPODOPHYLLOTOXIN-β-THENYLIDENE GLUCOSIDE (VM-26)(NSC-122819): A NEW DRUG FOR NEUROBLASTOMA (1977) (1)
Evaluation of azapicyl in soft tissue sarcomas in children: a report from the Children's Cancer Study Group. (1982) (1)
Pharmacokinetics of vincristine and cis-platinum in an anephric patient with metastatic Wilm's tumor (1979) (1)
A new kindred with hemoglobin Malmö (β97→Gln) (1976) (1)
855 HEMOSTATIC ABNORMALITIES AND THROMBOSIS DURING L-ASPARAGINASE (L-asp) THERAPY FOR ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) (1981) (1)
Complex α-thalassemia-like syndrome: A cause of neonatal normoblastemia (1976) (1)
Letter: A new kindred with hemoglobin Malmö (beta97 leads to Gln). (1976) (1)
1671 PULMONARY ENDOCRINE-LIKE CELLS IN HYALINE MEMBRANE DISEASE AND BRONCHOPULMONARY DYSPLASIA (1981) (1)
Single dose total body irradiation with high dose rate X-ray in combination with cyclophosphamide for bone marrow transplantation in acute nonlymphocytic leukemia initial remission (1981) (1)
Neutrophil surface antigen phenotyping: A new way to characterize autoimmune neutropenia (1980) (1)
Mechanism of action of vincristine sulfate. Abstr. (1968) (1)
GRISEOFULVIN THERAPY AS A CAUSE OF LYMPH NODE PROLIFERATION RESEMBLING MALIGNANT HISTIOCYTOSIS (1977) (1)
Treatment of High Risk Childhood Onset Cerebral Adrenoleukodystrophy (COCALD) with Modified Hematopoietic Stem Cell Transplantation (HSCT) • 1893 (1998) (1)
URINARY COPROPORPHYRIN EXCRETION IN CHILDHOOD ACUTE LEUKEMIA. (1965) (1)
AUTONOMOUS PRODUCTION OF PARATHORMONE BY LYMPHOBLASTIC LEUKEMIA CELLS IN CULTURE (1977) (1)
Brain catalase activity following syngeneic bone marrow transplantation in acatalasemic mice. (1986) (1)
GENETICS IN ACUTE LYMPHATIC LEUKEMIA IN CHILDHOOD * (1968) (1)
NEEDLE BIOPSY OF THE LIVER IN INFANCY AND CHILDHOOD (1967) (1)
Prognosis of fetuses at 33 weeks' gestation in Rh-sensitized women who have had preceding stillbirths. (1959) (1)
Comparison of vincristine utilized simultaneously or 24 hours before cyclophosphamide in maintenance regimen of acute lymphoblastic leukemia of children: a report of Childrens Cancer Study Group. (1981) (1)
GENETICS IN ACUTE LYMPHATIC LEUKEMIA IN CHILDHOOD * (1969) (0)
HYPERLIPIDÆMIA AFTER RENAL TRANSPLANTATION: SECONDARY TO VIRUS INFECTION? (1974) (0)
days attd prednisone for one month. A brief re view of the literature regarding the occurrence and nature of acquired coagulation factor inhibitors and the role of flnmunosuppressive therapy is also presented. (1978) (0)
Bone marrow transplantation for non-Hodgkin's lymphoma in children and young adults. A pilot study (1983) (0)
659 HERIDITARY ELLIPTOCYTOSIS, RED CELL FRAGMENTATION, AND DECREASED GLUTATHIONE (GSH) (1978) (0)
Letter: Hyperlipidaemia after renal transplantation: secondary to virus infection? (1974) (0)
672 SUCCESSFUL BONE MARROW TRANSPLANTATION (BMT) FOR APLASTIC ANEMIA WITH AN HLA-MLC NON-IDENTICAL PARENT DONOR (1978) (0)
Variations of diabetes insipidus associated with histiocytosis X. (1969) (0)
1334 THE EFFECT OF ANTENATAL ADMINISTRATION OF BETAMETHASONE ON THE HOSPITAL COSTS AND SURVIVAL OF PREMATURE INFANTS (1981) (0)
Phase II study of vindesine in the treatment of pediatric patients with solid tumors: a report from the Childrens Cancer Study Group. (1986) (0)
Phase II trial of dianhydrogalactitol in the treatment of children with refractory childhood malignancies: a report from the Children's Cancer Study Group. (1985) (0)
Hematopoietic Stem Cell Transplantation, Stem Cells, and Gene Therapy (2006) (0)
#640 Modified hematopoietic stem cell transplant (HSCT) preparative theraphy for high risk childhood onset cerebral adrenoleukodystrophy (COCALD) (1998) (0)
58 Factors affecting development of carpal tunnel syndrome in patients with Hurler syndrome after hematopoietic cell transplantation (2007) (0)
428 THE ONTOOENY OF THE RESPONSE TO GROWTH HORMONE (1985) (0)
remission: analysis of prognostic factors Bone marrow transplantation for acute nonlymphocytic leukemia in first (2011) (0)
Hereditary lymphedema jaundice and obstructive (1971) (0)
Malignant bone tumors in children. Recent advances in the treatment. (1974) (0)
Adrenoleukodystrophy: A Scoring .Method for Brain (2013) (0)
913 PREVENTION OF CYCLOPHOSPHAMIDE (CY) INDUCED HEMORRHAGIC CYSTITIS: UPDATE ON THE USE OF ASCORBIC ACID (AA) TO REDUCE URINARY (1985) (0)
Total body irradiation with a high dose rate linear accelerator for bone-marrow transplantation in children (1978) (0)
Bone marrow transplantation in hurler syndrome: Factors predictive of favorable outcome (1997) (0)
The development of malignant reticuloendotheliosis in the course of Wiskott-Aldrich syndrome (1965) (0)
640 VIRAL INDUCED HISTIOCYTIC MEDULLARY RETICULOSIS (1978) (0)
An experimental model of hemolytic thrombocytopenia uremic syndrome utilizing massive dosage of intravenous neuraminidase in rats (1979) (0)
A review of outcomes in 180 patients treated by hematopoietic cell transplantation (HCT) for lysosomal and peroxisomal diseases in the past 18 years at the University of Minnesota (2000) (0)
5Unrelated umbilical cord blood transplantation for hurler syndrome (2003) (0)
DONOR BONE MARROW-DERIVED CELLS TRANSFORM INTO RAMIFIED MICROGLIA IN THE ADULT CNS (1996) (0)
571 CONSERVATIVE MANAGEMENT OF ESOPHAGEAL AND PHARYNGEAL PERFORATIONS IN THE NEWBORN (1981) (0)
HLA IN A PEDIGREE WITH IMMUNOLOGIC AND ENDOCRINE DISEASE (1977) (0)
622 ERYTHROGENESIS IMPERFECTA IN SEVEN INDIVIDUALS IN THREE GENERATIONS (1978) (0)
Bone marrow transplantation for severe aplastic anemia following preparation with cyclophosphamide and total lymphoid irradiation. (1984) (0)
SUPPRESSION OF MYELOPOIESIS IN THE SOFT AGAR CULTURE SYSTEM IN A PATIENT WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH) AND APLASTIC ANEMIA (AA) (1977) (0)
Report of 100 hurler syndrome patients receiving 115 bone marrow transplants (1996) (0)
Phase II evaluation of diglycoaldehyde (Inox) in children with acute leukemia: a children's cancer study group report. (1980) (0)
1275 NEW ROLE OF COMPUTERIZED TOMOGRAPHY IN THE ASSESSMENT OF INBORN ERRORS OF METABOLISM (1985) (0)
RED BLOOD CELL (RBC) ABNORMALITIES IN CHRONIC GRANULOMATOUS DISEASE (CGD) WITH MCLEOD PHENOTYPE (1977) (0)
The influence of maternal iron overload on mature rat offspring (1977) (0)

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