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The Journal of Experimental Medicine
|
June 4, 2008
Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infants
Sandra Weller, Maria Mamani-Matsuda, Capucine Picard, et al.
Frontiers in Immunology
|
April 25, 2018
Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation
Fabienne Mazerolles, Marie-Claude Stolzenberg, Olivier Pelle, et al.
Journal of the American Academy of Dermatology
|
June 28, 2011
Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: a retrospective, single-center study of 21 patients diagnosed using molecular analysis
Amani Olaiwan, Marie-Olivia Chandesris, Sylvie Fraitag, et al.
The Journal of Allergy and Clinical Immunology
|
May 7, 2011
Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency
Vincent Barlogis, Claire Galambrun, Hervé Chambost, et al.
EMBO Molecular Medicine
|
December 29, 2017
Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility
Sarah Winter, Emmanuel Martin, David Boutboul, et al.
Lancet (London, England)
|
May 7, 2013
Pachymeningitis after meningococcal infection
Julie Toubiana, Claire Heilbronner, Cyril Gitiaux, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
October 21, 2005
Septicemia without sepsis: inherited disorders of nuclear factor-kappa B-mediated inflammation
Horst von Bernuth, Anne Puel, Cheng-Lung Ku, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2018
Next generation phenotyping using narrative reports in a rare disease clinical data warehouse
Nicolas Garcelon, Antoine Neuraz, Rémi Salomon, et al.
Pediatric Dermatology
|
September 7, 2018
Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome
Sarah Law-Ping-Man, Fabienne Toutain, Frédéric Rieux-Laucat, et al.
Frontiers in Pediatrics
|
May 16, 2017
IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Karina Gobin, Mary Hintermeyer, Bertrand Boisson, et al.
Page
of 40
Search research articles
Search
Showing results (61-70 of 400) with videos related to
Sort By:
Page
of 40
The Journal of Experimental Medicine
|
June 4, 2008
Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infants
Sandra Weller, Maria Mamani-Matsuda, Capucine Picard, et al.
Frontiers in Immunology
|
April 25, 2018
Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation
Fabienne Mazerolles, Marie-Claude Stolzenberg, Olivier Pelle, et al.
Journal of the American Academy of Dermatology
|
June 28, 2011
Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: a retrospective, single-center study of 21 patients diagnosed using molecular analysis
Amani Olaiwan, Marie-Olivia Chandesris, Sylvie Fraitag, et al.
The Journal of Allergy and Clinical Immunology
|
May 7, 2011
Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency
Vincent Barlogis, Claire Galambrun, Hervé Chambost, et al.
EMBO Molecular Medicine
|
December 29, 2017
Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility
Sarah Winter, Emmanuel Martin, David Boutboul, et al.
Lancet (London, England)
|
May 7, 2013
Pachymeningitis after meningococcal infection
Julie Toubiana, Claire Heilbronner, Cyril Gitiaux, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
October 21, 2005
Septicemia without sepsis: inherited disorders of nuclear factor-kappa B-mediated inflammation
Horst von Bernuth, Anne Puel, Cheng-Lung Ku, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2018
Next generation phenotyping using narrative reports in a rare disease clinical data warehouse
Nicolas Garcelon, Antoine Neuraz, Rémi Salomon, et al.
Pediatric Dermatology
|
September 7, 2018
Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome
Sarah Law-Ping-Man, Fabienne Toutain, Frédéric Rieux-Laucat, et al.
Frontiers in Pediatrics
|
May 16, 2017
IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Karina Gobin, Mary Hintermeyer, Bertrand Boisson, et al.
Page
of 40