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Blood Cells
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January 1, 1978
Beta thalassemia with reticulocytopenia: clinical, biochemical, and ultrastructural studies
Y Beuzard, M Tulliez, J Breton-Gorius, et al.
Blood
|
October 15, 1993
Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A
J L Stéphan, J Donadieu, F Ledeist, et al.
American Journal of Human Genetics
|
May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome
B Arveiler, G de Saint-Basile, A Fischer, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1977
A second case of inosine phosphorylase deficiency with severe T-cell abnormalities
M Hamet, C Griscelli, P Cartier, et al.
Archives Francaises De Pediatrie
|
May 1, 1982
[Familial sarcoid arthritis ]
A M Prieur, C J Menkes, J L Bessis, et al.
Gastroenterologie Clinique Et Biologique
|
December 1, 1982
[Intestinal cryptosporidiosis : a new cause of diarrhea in man?]
F Arnaud-Battandier, M Naceri, A Fischer, et al.
Journal of Clinical Immunology
|
March 1, 1989
Activation of genetically major histocompatibility complex (MHC) class II-deficient B lymphocytes
A Durandy, M Mangeney, C Griscelli, et al.
Human Molecular Genetics
|
June 1, 1994
Two complementation groups account for most cases of inherited MHC class II deficiency
B Lisowska-Grospierre, M C Fondaneche, M P Rols, et al.
The American Journal of Pathology
|
May 1, 1980
Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections. Detection by immunoperoxidase staining for lactoferrin and cytochemical electron microscopy
J Breton-Gorius, D Y Mason, D Buriot, et al.
Acta Paediatrica Scandinavica
|
November 1, 1987
Megaloblastic anemia and immune abnormalities in a patient with methionine synthase deficiency
J Zittoun, A Fischer, J Marquet, et al.
Page
of 36
Search research articles
Search
Showing results (201-210 of 358) with videos related to
Sort By:
Page
of 36
Blood Cells
|
January 1, 1978
Beta thalassemia with reticulocytopenia: clinical, biochemical, and ultrastructural studies
Y Beuzard, M Tulliez, J Breton-Gorius, et al.
Blood
|
October 15, 1993
Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A
J L Stéphan, J Donadieu, F Ledeist, et al.
American Journal of Human Genetics
|
May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome
B Arveiler, G de Saint-Basile, A Fischer, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1977
A second case of inosine phosphorylase deficiency with severe T-cell abnormalities
M Hamet, C Griscelli, P Cartier, et al.
Archives Francaises De Pediatrie
|
May 1, 1982
[Familial sarcoid arthritis ]
A M Prieur, C J Menkes, J L Bessis, et al.
Gastroenterologie Clinique Et Biologique
|
December 1, 1982
[Intestinal cryptosporidiosis : a new cause of diarrhea in man?]
F Arnaud-Battandier, M Naceri, A Fischer, et al.
Journal of Clinical Immunology
|
March 1, 1989
Activation of genetically major histocompatibility complex (MHC) class II-deficient B lymphocytes
A Durandy, M Mangeney, C Griscelli, et al.
Human Molecular Genetics
|
June 1, 1994
Two complementation groups account for most cases of inherited MHC class II deficiency
B Lisowska-Grospierre, M C Fondaneche, M P Rols, et al.
The American Journal of Pathology
|
May 1, 1980
Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections. Detection by immunoperoxidase staining for lactoferrin and cytochemical electron microscopy
J Breton-Gorius, D Y Mason, D Buriot, et al.
Acta Paediatrica Scandinavica
|
November 1, 1987
Megaloblastic anemia and immune abnormalities in a patient with methionine synthase deficiency
J Zittoun, A Fischer, J Marquet, et al.
Page
of 36