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The Journal of Allergy and Clinical Immunology
|
November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features
Nigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.
Eye (London, England)
|
May 24, 2023
Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome
Brian G Ballios, Amarilla Mandola, Alaa Tayyib, et al.
Pediatric Research
|
January 9, 2004
Purine nucleoside phosphorylase deficiency associated with a dysplastic marrow morphology
Yigal Dror, Eyal Grunebaum, Johann Hitzler, et al.
The Journal of Pediatrics
|
February 1, 1992
Prognostic indicators of joint destruction in systemic-onset juvenile rheumatoid arthritis
R Schneider, B A Lang, B J Reilly, et al.
Molecular Immunology
|
June 1, 1991
Expression of the human T cell receptor V beta repertoire
P J Doherty, C M Roifman, S H Pan, et al.
Human Molecular Genetics
|
April 1, 1995
Mutation analysis in Bruton's tyrosine kinase, the X-linked agammaglobulinaemia gene, including identification of an insertional hotspot
H B Gaspar, L A Bradley, F Katz, et al.
The Journal of Clinical Investigation
|
May 1, 1990
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings
M E Conley, R H Buckley, R Hong, et al.
International Immunopharmacology
|
August 2, 2003
Comparison of the efficacy of IGIV-C, 10% (caprylate/chromatography) and IGIV-SD, 10% as replacement therapy in primary immune deficiency. A randomized double-blind trial
Chaim M Roifman, Harry Schroeder, Melvin Berger, et al.
The Journal of Allergy and Clinical Immunology
|
May 3, 2011
Purine metabolism, immune reconstitution, and abdominal adipose tumor after gene therapy for adenosine deaminase deficiency
Eyal Grunebaum, Catherine T-S Chung, Harjit Dadi, et al.
NPJ Genomic Medicine
|
December 22, 2017
A homozygous mutation in the stem II domain of <i>RNU4ATAC</i> causes typical Roifman syndrome
Yael Dinur Schejter, Adi Ovadia, Roumiana Alexandrova, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 225) with videos related to
Sort By:
Page
of 23
The Journal of Allergy and Clinical Immunology
|
November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features
Nigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.
Eye (London, England)
|
May 24, 2023
Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome
Brian G Ballios, Amarilla Mandola, Alaa Tayyib, et al.
Pediatric Research
|
January 9, 2004
Purine nucleoside phosphorylase deficiency associated with a dysplastic marrow morphology
Yigal Dror, Eyal Grunebaum, Johann Hitzler, et al.
The Journal of Pediatrics
|
February 1, 1992
Prognostic indicators of joint destruction in systemic-onset juvenile rheumatoid arthritis
R Schneider, B A Lang, B J Reilly, et al.
Molecular Immunology
|
June 1, 1991
Expression of the human T cell receptor V beta repertoire
P J Doherty, C M Roifman, S H Pan, et al.
Human Molecular Genetics
|
April 1, 1995
Mutation analysis in Bruton's tyrosine kinase, the X-linked agammaglobulinaemia gene, including identification of an insertional hotspot
H B Gaspar, L A Bradley, F Katz, et al.
The Journal of Clinical Investigation
|
May 1, 1990
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings
M E Conley, R H Buckley, R Hong, et al.
International Immunopharmacology
|
August 2, 2003
Comparison of the efficacy of IGIV-C, 10% (caprylate/chromatography) and IGIV-SD, 10% as replacement therapy in primary immune deficiency. A randomized double-blind trial
Chaim M Roifman, Harry Schroeder, Melvin Berger, et al.
The Journal of Allergy and Clinical Immunology
|
May 3, 2011
Purine metabolism, immune reconstitution, and abdominal adipose tumor after gene therapy for adenosine deaminase deficiency
Eyal Grunebaum, Catherine T-S Chung, Harjit Dadi, et al.
NPJ Genomic Medicine
|
December 22, 2017
A homozygous mutation in the stem II domain of <i>RNU4ATAC</i> causes typical Roifman syndrome
Yael Dinur Schejter, Adi Ovadia, Roumiana Alexandrova, et al.
Page
of 23