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Alain Fischer

Showing results (391-400 of 493) with videos related to

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Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 25, 2012
RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutationsAlessandra Pangrazio, Barbara Cassani, Matteo M Guerrini, et al.
Blood|January 28, 2015
Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter studyMieke Aldenhoven, Robert F Wynn, Paul J Orchard, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Nature Immunology|November 17, 2016
Corrigendum: Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
Blood|April 9, 2010
Clinical and immunologic outcome of patients with cartilage hair hypoplasia after hematopoietic stem cell transplantationVictoria Bordon, Andrew R Gennery, Mary A Slatter, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) studyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
Blood|June 28, 2014
Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patientsBénédicte Neven, Julie Bruneau, Marie-Claude Stolzenberg, et al.
Gastroenterology|June 12, 2010
Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathyNicolette Moes, Frédéric Rieux-Laucat, Bernadette Begue, et al.
The Journal of Clinical Investigation|December 3, 2013
TTC7A mutations disrupt intestinal epithelial apicobasal polarityAmélie E Bigorgne, Henner F Farin, Roxane Lemoine, et al.
Pageof 50

Showing results (391-400 of 493) with videos related to

Sort By:
Pageof 50
Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 25, 2012
RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutationsAlessandra Pangrazio, Barbara Cassani, Matteo M Guerrini, et al.
Blood|January 28, 2015
Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter studyMieke Aldenhoven, Robert F Wynn, Paul J Orchard, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Nature Immunology|November 17, 2016
Corrigendum: Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
Blood|April 9, 2010
Clinical and immunologic outcome of patients with cartilage hair hypoplasia after hematopoietic stem cell transplantationVictoria Bordon, Andrew R Gennery, Mary A Slatter, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) studyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
Blood|June 28, 2014
Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patientsBénédicte Neven, Julie Bruneau, Marie-Claude Stolzenberg, et al.
Gastroenterology|June 12, 2010
Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathyNicolette Moes, Frédéric Rieux-Laucat, Bernadette Begue, et al.
The Journal of Clinical Investigation|December 3, 2013
TTC7A mutations disrupt intestinal epithelial apicobasal polarityAmélie E Bigorgne, Henner F Farin, Roxane Lemoine, et al.
Pageof 50