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Pediatrics
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February 1, 1994
Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course
E 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 syndrome
G 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 genes
C 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 phenotype
G 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 lymphocytes
A Fischer, A Durandy, J L Virelizier, et al.
European Cytokine Network
|
June 5, 1998
Inflammation: "a natural experiment" for the systemic pathogenicity of cytokines
C 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 prodrome
W 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 lymphocytes
M 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.
Page
of 36
Search research articles
Search
Showing results (291-300 of 358) with videos related to
Sort By:
Page
of 36
Pediatrics
|
February 1, 1994
Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course
E 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 syndrome
G 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 genes
C 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 phenotype
G 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 lymphocytes
A Fischer, A Durandy, J L Virelizier, et al.
European Cytokine Network
|
June 5, 1998
Inflammation: "a natural experiment" for the systemic pathogenicity of cytokines
C 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 prodrome
W 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 lymphocytes
M 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.
Page
of 36