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Hematology/Oncology and Stem Cell Therapy
|
December 17, 2013
Severe combined immunodeficiency caused by a new homozygous RAG1 mutation with progressive encephalopathy
Nivedita Dhingra, Satya Prakash Yadav, Jean-Pierre de Villartay, et al.
Human Molecular Genetics
|
April 17, 2018
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state
Guillaume Velasco, Giacomo Grillo, Nizar Touleimat, et al.
Blood Cells, Molecules & Diseases
|
April 3, 2007
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR
Alexis Proust, Benoît Guillet, Capucine Picard, et al.
Biochimie
|
June 15, 2007
Human primary immunodeficiencies of type I interferons
Emmanuelle Jouanguy, Shen-Ying Zhang, Ariane Chapgier, et al.
Case Reports in Immunology
|
November 7, 2014
Variant of X-Linked Chronic Granulomatous Disease Revealed by a Severe Burkholderia cepacia Invasive Infection in an Infant
Saul Oswaldo Lugo Reyes, Nizar Mahlaoui, Carolina Prando, et al.
British Journal of Haematology
|
July 20, 2006
Human leucocyte antigen-identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft-versus-host disease and pre-existing viral infections
Raffaele Renella, Capucine Picard, Bénédicte Neven, et al.
Immunological Reviews
|
November 6, 2007
Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses
Shen-Ying Zhang, Emmanuelle Jouanguy, Vanessa Sancho-Shimizu, et al.
Frontiers in Pediatrics
|
March 14, 2018
Corrigendum: IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Karina S Gobin, Mary Hintermeyer, Bertrand Boisson, et al.
The American Journal of Tropical Medicine and Hygiene
|
September 24, 2014
Imported African histoplasmosis in an immunocompetent patient 40 years after staying in a disease-endemic area
Clémence Richaud, Marie-Olivia Chandesris, Fanny Lanternier, et al.
Journal of Human Genetics
|
June 7, 2013
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients
Hirohisa Nitta, Motoko Unoki, Kenji Ichiyanagi, et al.
Page
of 40
Search research articles
Search
Showing results (71-80 of 400) with videos related to
Sort By:
Page
of 40
Hematology/Oncology and Stem Cell Therapy
|
December 17, 2013
Severe combined immunodeficiency caused by a new homozygous RAG1 mutation with progressive encephalopathy
Nivedita Dhingra, Satya Prakash Yadav, Jean-Pierre de Villartay, et al.
Human Molecular Genetics
|
April 17, 2018
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state
Guillaume Velasco, Giacomo Grillo, Nizar Touleimat, et al.
Blood Cells, Molecules & Diseases
|
April 3, 2007
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR
Alexis Proust, Benoît Guillet, Capucine Picard, et al.
Biochimie
|
June 15, 2007
Human primary immunodeficiencies of type I interferons
Emmanuelle Jouanguy, Shen-Ying Zhang, Ariane Chapgier, et al.
Case Reports in Immunology
|
November 7, 2014
Variant of X-Linked Chronic Granulomatous Disease Revealed by a Severe Burkholderia cepacia Invasive Infection in an Infant
Saul Oswaldo Lugo Reyes, Nizar Mahlaoui, Carolina Prando, et al.
British Journal of Haematology
|
July 20, 2006
Human leucocyte antigen-identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft-versus-host disease and pre-existing viral infections
Raffaele Renella, Capucine Picard, Bénédicte Neven, et al.
Immunological Reviews
|
November 6, 2007
Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses
Shen-Ying Zhang, Emmanuelle Jouanguy, Vanessa Sancho-Shimizu, et al.
Frontiers in Pediatrics
|
March 14, 2018
Corrigendum: IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Karina S Gobin, Mary Hintermeyer, Bertrand Boisson, et al.
The American Journal of Tropical Medicine and Hygiene
|
September 24, 2014
Imported African histoplasmosis in an immunocompetent patient 40 years after staying in a disease-endemic area
Clémence Richaud, Marie-Olivia Chandesris, Fanny Lanternier, et al.
Journal of Human Genetics
|
June 7, 2013
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients
Hirohisa Nitta, Motoko Unoki, Kenji Ichiyanagi, et al.
Page
of 40