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Blood
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February 1, 1997
Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: a molecular and immunological analysis
A Bettinardi, D Brugnoni, E Quiròs-Roldan, et al.
The American Journal of Surgical Pathology
|
June 1, 1996
The pathology of Omenn's syndrome
M Chilosi, F Facchetti, L D Notarangelo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 6, 2006
Common polymorphisms of the growth hormone (GH) receptor do not correlate with the growth response to exogenous recombinant human GH in GH-deficient children
A Pilotta, P Mella, M Filisetti, et al.
Clinical and Experimental Immunology
|
September 26, 2002
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation
A Tommasini, S Ferrari, D Moratto, et al.
Pediatric Hematology and Oncology
|
September 1, 1995
Effect of interferon-alpha therapy in a patient with common variable immunodeficiency and chronic Epstein-Barr virus infection
R Toraldo, M D'Avanzo, C Tolone, et al.
The American Journal of Pathology
|
January 23, 1999
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions
F Facchetti, W Vermi, S Fiorentini, et al.
Life Sciences
|
January 1, 1997
A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies
G S Wengler, O Parolini, M Fiorini, et al.
The Journal of Experimental Medicine
|
June 1, 1996
In vitro correction of JAK3-deficient severe combined immunodeficiency by retroviral-mediated gene transduction
F Candotti, S A Oakes, J A Johnston, et al.
The Journal of Clinical Investigation
|
June 1, 1996
Studies of the expression of the Wiskott-Aldrich syndrome protein
D M Stewart, S Treiber-Held, C C Kurman, et al.
Allergy
|
August 5, 2004
Toll-like receptor-4 genotype in children with respiratory infections
R Badolato, S Fontana, L Barcella, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 165) with videos related to
Sort By:
Page
of 17
Blood
|
February 1, 1997
Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: a molecular and immunological analysis
A Bettinardi, D Brugnoni, E Quiròs-Roldan, et al.
The American Journal of Surgical Pathology
|
June 1, 1996
The pathology of Omenn's syndrome
M Chilosi, F Facchetti, L D Notarangelo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 6, 2006
Common polymorphisms of the growth hormone (GH) receptor do not correlate with the growth response to exogenous recombinant human GH in GH-deficient children
A Pilotta, P Mella, M Filisetti, et al.
Clinical and Experimental Immunology
|
September 26, 2002
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation
A Tommasini, S Ferrari, D Moratto, et al.
Pediatric Hematology and Oncology
|
September 1, 1995
Effect of interferon-alpha therapy in a patient with common variable immunodeficiency and chronic Epstein-Barr virus infection
R Toraldo, M D'Avanzo, C Tolone, et al.
The American Journal of Pathology
|
January 23, 1999
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions
F Facchetti, W Vermi, S Fiorentini, et al.
Life Sciences
|
January 1, 1997
A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies
G S Wengler, O Parolini, M Fiorini, et al.
The Journal of Experimental Medicine
|
June 1, 1996
In vitro correction of JAK3-deficient severe combined immunodeficiency by retroviral-mediated gene transduction
F Candotti, S A Oakes, J A Johnston, et al.
The Journal of Clinical Investigation
|
June 1, 1996
Studies of the expression of the Wiskott-Aldrich syndrome protein
D M Stewart, S Treiber-Held, C C Kurman, et al.
Allergy
|
August 5, 2004
Toll-like receptor-4 genotype in children with respiratory infections
R Badolato, S Fontana, L Barcella, et al.
Page
of 17