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Results: 1-7 |
Results: 7
RENAL-TRANSPLANTATION IN C3 DEFICIENCY
Authors: FIVUSH B STRAUCH E AMERATUNGA R WINKELSTEIN J NEU A COLOMBANI P
Citation: B. Fivush et al., RENAL-TRANSPLANTATION IN C3 DEFICIENCY, Journal of allergy and clinical immunology, 99(1), 1997, pp. 2038-2038
RENAL-TRANSPLANTATION IN C3 DEFICIENCY
Authors: FIVUSH B STRAUCH E AMERATUNGA R WINKELSTEIN J NEU A COLOMBANI P
Citation: B. Fivush et al., RENAL-TRANSPLANTATION IN C3 DEFICIENCY, Journal of allergy and clinical immunology, 99(1), 1997, pp. 2040-2040
SPLICE-SITE MUTATIONS IN THE WISKOTT-ALDRICH SYNDROME
Authors: LIU T ZHU OL BLAESE RM JUNKER SK WINKELSTEIN J OCHS HD
Citation: T. Liu et al., SPLICE-SITE MUTATIONS IN THE WISKOTT-ALDRICH SYNDROME, Pediatric research, 39(4), 1996, pp. 59-59
UNIQUE MUTATIONS OF BRUTON TYROSINE KINASE IN 14 UNRELATED X-LINKED AGAMMAGLOBULINEMIA FAMILIES
Authors: ZHU QL ZHANG M WINKELSTEIN J CHEN SH OCHS HD
Citation: Ql. Zhu et al., UNIQUE MUTATIONS OF BRUTON TYROSINE KINASE IN 14 UNRELATED X-LINKED AGAMMAGLOBULINEMIA FAMILIES, Human molecular genetics, 3(10), 1994, pp. 1899-1900
QUANTITATIVE DISCRIMINATION OF HEPATIC RETICULOENDOTHELIAL CLEARANCE AND PHAGOCYTIC KILLING
Authors: KLEIN A ZHADKEWICH M MARGOLICK J WINKELSTEIN J BULKLEY G
Citation: A. Klein et al., QUANTITATIVE DISCRIMINATION OF HEPATIC RETICULOENDOTHELIAL CLEARANCE AND PHAGOCYTIC KILLING, Journal of leukocyte biology, 55(2), 1994, pp. 248-252
DEVELOPMENT OF POSTSPLENECTOMY SEPSIS AND COMMON VARIABLE IMMUNODEFICIENCY IN A PATIENT WITH IMMUNE THROMBOCYTOPENIC PURPURA
Authors: FARUQI S GUHA B WINKELSTEIN J KRISHNASWAMY G
Citation: S. Faruqi et al., DEVELOPMENT OF POSTSPLENECTOMY SEPSIS AND COMMON VARIABLE IMMUNODEFICIENCY IN A PATIENT WITH IMMUNE THROMBOCYTOPENIC PURPURA, Journal of allergy and clinical immunology, 93(1), 1994, pp. 170-170
HEMOLYTICALLY INACTIVE C4B COMPLEMENT ALLOTYPE CAUSED BY A PROLINE TOLEUCINE MUTATION IN THE C5-BINDING SITE
Authors: MCLEAN RH NIBLACK G JULIAN B WANG T WYATT R PHILLIPS JA COLLINS TS WINKELSTEIN J VALLE D
Citation: Rh. Mclean et al., HEMOLYTICALLY INACTIVE C4B COMPLEMENT ALLOTYPE CAUSED BY A PROLINE TOLEUCINE MUTATION IN THE C5-BINDING SITE, The Journal of biological chemistry, 269(44), 1994, pp. 27727-27731
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