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J A Winkelstein

Showing results (101-110 of 151) with videos related to

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Veterinary Immunology and Immunopathology|December 1, 1988
Complement levels in dogs with familial canine dermatomyositisA M Hargis, J A Winkelstein, M P Moore, et al.
Clinical Immunology and Immunopathology|March 1, 1985
The clinical manifestations of a genetically determined deficiency of the third component of complement in the dogJ R Blum, L C Cork, J M Morris, et al.
American Journal of Hematology|January 1, 1978
Abnormalities of the peripheral blood as a presenting feature of immunodeficiencyV S Blanchette, J J Hallett, J M Hemphill, et al.
The Johns Hopkins Medical Journal|June 1, 1979
Non-candidal infections in children with chronic mucocutaneous candidiasisB E Chipps, F T Saulsbury, S H Hsu, et al.
The Pediatric Infectious Disease Journal|June 5, 1998
Recurrent Francisella philomiragia sepsis in chronic granulomatous diseaseF P Polack, S M Harrington, J A Winkelstein, et al.
The Journal of Rheumatology|June 1, 1994
Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosusK E Sullivan, M A Petri, B J Schmeckpeper, et al.
The Journal of Infectious Diseases|January 1, 1988
Chronic group A coxsackievirus infection in agammaglobulinemia: demonstration of genomic variation of serotypically identical isolates persistently excreted by the same patientK M O'Neil, M A Pallansch, J A Winkelstein, et al.
Infection and Immunity|November 1, 1986
The ability to sensitize host cells for destruction by autologous complement is a general property of lipoteichoic acidB D Weinreb, G D Shockman, E H Beachey, et al.
The Journal of Pediatrics|June 1, 1986
Pseudomonas cepacia: an emerging pathogen in chronic granulomatous diseaseK M O'Neil, J H Herman, J F Modlin, et al.
Lancet (London, England)|January 1, 1999
Immune constitution of complete DiGeorge anomaly by transplantation of unmobilised blood mononuclear cellsD C Bowers, H M Lederman, S H Sicherer, et al.
Pageof 16

Showing results (101-110 of 151) with videos related to

Sort By:
Pageof 16
Veterinary Immunology and Immunopathology|December 1, 1988
Complement levels in dogs with familial canine dermatomyositisA M Hargis, J A Winkelstein, M P Moore, et al.
Clinical Immunology and Immunopathology|March 1, 1985
The clinical manifestations of a genetically determined deficiency of the third component of complement in the dogJ R Blum, L C Cork, J M Morris, et al.
American Journal of Hematology|January 1, 1978
Abnormalities of the peripheral blood as a presenting feature of immunodeficiencyV S Blanchette, J J Hallett, J M Hemphill, et al.
The Johns Hopkins Medical Journal|June 1, 1979
Non-candidal infections in children with chronic mucocutaneous candidiasisB E Chipps, F T Saulsbury, S H Hsu, et al.
The Pediatric Infectious Disease Journal|June 5, 1998
Recurrent Francisella philomiragia sepsis in chronic granulomatous diseaseF P Polack, S M Harrington, J A Winkelstein, et al.
The Journal of Rheumatology|June 1, 1994
Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosusK E Sullivan, M A Petri, B J Schmeckpeper, et al.
The Journal of Infectious Diseases|January 1, 1988
Chronic group A coxsackievirus infection in agammaglobulinemia: demonstration of genomic variation of serotypically identical isolates persistently excreted by the same patientK M O'Neil, M A Pallansch, J A Winkelstein, et al.
Infection and Immunity|November 1, 1986
The ability to sensitize host cells for destruction by autologous complement is a general property of lipoteichoic acidB D Weinreb, G D Shockman, E H Beachey, et al.
The Journal of Pediatrics|June 1, 1986
Pseudomonas cepacia: an emerging pathogen in chronic granulomatous diseaseK M O'Neil, J H Herman, J F Modlin, et al.
Lancet (London, England)|January 1, 1999
Immune constitution of complete DiGeorge anomaly by transplantation of unmobilised blood mononuclear cellsD C Bowers, H M Lederman, S H Sicherer, et al.
Pageof 16