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C Griscelli

Showing results (291-300 of 358) with videos related to

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Pediatrics|February 1, 1994
Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural courseE J Gerritsen, J M Vossen, I H van Loo, et al.
Blood|May 1, 1985
Enhanced plasminogen-activator production by leukocytes in the human and murine Chediak-Higashi syndromeG de Saint Basile, A Fischer, M D Dautzenberg, et al.
Clinical Immunology and Immunopathology|January 1, 1989
Combined immunodeficiency with abnormal expression of MHC class II genesC Griscelli, B Lisowska-Grospierre, F Le Deist, et al.
Human Genetics|September 1, 1988
Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotypeG de Saint-Basile, M C Bohler, A Fischer, et al.
The Journal of Pediatrics|August 1, 1981
Severe combined immunodeficiency with quantitatively normal but abnormally differentiated T lymphocytesA Fischer, A Durandy, J L Virelizier, et al.
European Cytokine Network|June 5, 1998
Inflammation: "a natural experiment" for the systemic pathogenicity of cytokinesC Herbelin, P Roux-Lombard, A Herbelin, et al.
Lancet (London, England)|February 23, 1985
Antimoniotungstate (HPA 23) treatment of three patients with AIDS and one with prodromeW Rozenbaum, D Dormont, B Spire, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1990
Human severe combined immunodeficiency disease: phenotypic and functional characteristics of peripheral B lymphocytesM L Gougeon, G Drean, F Le Deist, et al.
Archives Francaises De Pediatrie|November 1, 1984
[Treatment of the Wiskott-Aldrich syndrome by a graft of allogeneic bone marrow]A Fischer, A Durandy, P Bordigoni, et al.
Archives Francaises De Pediatrie|April 1, 1992
[Treatment of adenosine deaminase deficiency with adenosine deaminase combined with polyethylene glycol]D Girault, F Le Deist, M Debré, et al.
Pageof 36

Showing results (291-300 of 358) with videos related to

Sort By:
Pageof 36
Pediatrics|February 1, 1994
Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural courseE J Gerritsen, J M Vossen, I H van Loo, et al.
Blood|May 1, 1985
Enhanced plasminogen-activator production by leukocytes in the human and murine Chediak-Higashi syndromeG de Saint Basile, A Fischer, M D Dautzenberg, et al.
Clinical Immunology and Immunopathology|January 1, 1989
Combined immunodeficiency with abnormal expression of MHC class II genesC Griscelli, B Lisowska-Grospierre, F Le Deist, et al.
Human Genetics|September 1, 1988
Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotypeG de Saint-Basile, M C Bohler, A Fischer, et al.
The Journal of Pediatrics|August 1, 1981
Severe combined immunodeficiency with quantitatively normal but abnormally differentiated T lymphocytesA Fischer, A Durandy, J L Virelizier, et al.
European Cytokine Network|June 5, 1998
Inflammation: "a natural experiment" for the systemic pathogenicity of cytokinesC Herbelin, P Roux-Lombard, A Herbelin, et al.
Lancet (London, England)|February 23, 1985
Antimoniotungstate (HPA 23) treatment of three patients with AIDS and one with prodromeW Rozenbaum, D Dormont, B Spire, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1990
Human severe combined immunodeficiency disease: phenotypic and functional characteristics of peripheral B lymphocytesM L Gougeon, G Drean, F Le Deist, et al.
Archives Francaises De Pediatrie|November 1, 1984
[Treatment of the Wiskott-Aldrich syndrome by a graft of allogeneic bone marrow]A Fischer, A Durandy, P Bordigoni, et al.
Archives Francaises De Pediatrie|April 1, 1992
[Treatment of adenosine deaminase deficiency with adenosine deaminase combined with polyethylene glycol]D Girault, F Le Deist, M Debré, et al.
Pageof 36