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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.
The New England Journal of Medicine
|
August 28, 1986
Expression of the gene defect in X-linked agammaglobulinemia
M E Conley, P Brown, A R Pickard, et al.
Genomics
|
February 1, 1993
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22
O Parolini, J F Hejtmancik, R C Allen, et al.
Bone Marrow Transplantation
|
May 1, 1996
Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry
T G Gross, A H Filipovich, M E Conley, et al.
The New England Journal of Medicine
|
November 14, 1996
Mutations in the mu heavy-chain gene in patients with agammaglobulinemia
L Yel, Y Minegishi, E Coustan-Smith, et al.
The Journal of Clinical Investigation
|
October 1, 1994
Hyper IgM syndrome associated with defective CD40-mediated B cell activation
M E Conley, M Larché, V R Bonagura, et al.
Journal of Investigational Allergology & Clinical Immunology
|
September 13, 2011
Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulin
L M Endo, J V Giannobile, A K Dobbs, et al.
The Journal of Clinical Investigation
|
January 1, 1996
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome
Q Lin, J Rohrer, R C Allen, et al.
Clinical Immunology (Orlando, Fla.)
|
December 9, 2000
Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome
Y Minegishi, A Lavoie, C Cunningham-Rundles, et al.
Genomics
|
November 1, 1987
Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man
R F Holcombe, W Strauss, F L Owen, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 116) with videos related to
Sort By:
Page
of 12
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.
The New England Journal of Medicine
|
August 28, 1986
Expression of the gene defect in X-linked agammaglobulinemia
M E Conley, P Brown, A R Pickard, et al.
Genomics
|
February 1, 1993
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22
O Parolini, J F Hejtmancik, R C Allen, et al.
Bone Marrow Transplantation
|
May 1, 1996
Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry
T G Gross, A H Filipovich, M E Conley, et al.
The New England Journal of Medicine
|
November 14, 1996
Mutations in the mu heavy-chain gene in patients with agammaglobulinemia
L Yel, Y Minegishi, E Coustan-Smith, et al.
The Journal of Clinical Investigation
|
October 1, 1994
Hyper IgM syndrome associated with defective CD40-mediated B cell activation
M E Conley, M Larché, V R Bonagura, et al.
Journal of Investigational Allergology & Clinical Immunology
|
September 13, 2011
Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulin
L M Endo, J V Giannobile, A K Dobbs, et al.
The Journal of Clinical Investigation
|
January 1, 1996
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome
Q Lin, J Rohrer, R C Allen, et al.
Clinical Immunology (Orlando, Fla.)
|
December 9, 2000
Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome
Y Minegishi, A Lavoie, C Cunningham-Rundles, et al.
Genomics
|
November 1, 1987
Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man
R F Holcombe, W Strauss, F L Owen, et al.
Page
of 12