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Peyrard

Showing results (271-280 of 289) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 20, 2012
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA InvestigatorsAnne-Paule Gimenez-Roqueplo, Aurore Caumont-Prim, Claire Houzard, et al.
EMBO Molecular Medicine|January 25, 2023
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotypeBérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar, et al.
Circulation|September 15, 2010
Composite cell sheets: a further step toward safe and effective myocardial regeneration by cardiac progenitors derived from embryonic stem cellsAlain Bel, Valérie Planat-Bernard, Atsuhiro Saito, et al.
Blood|March 16, 2025
The neutrophil antigen 3a/b polymorphism in SLC44A2 unexpectedly encodes Csa/Csb red cell antigensRomain Duval, Alissa Soudry, Jonathan De Oliveira Rios, et al.
Blood|March 25, 2021
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disordersRomain Duval, Gaël Nicolas, Alexandra Willemetz, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.
ISBT Science Series|November 3, 2017
International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetingsJ R Storry, L Castilho, Q Chen, et al.
Blood|December 12, 2019
Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregationSlim Azouzi, Mahmoud Mikdar, Patricia Hermand, et al.
Vox Sanguinis|November 14, 2018
International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetingsJill R Storry, Frederik Banch Clausen, Lilian Castilho, et al.
Pageof 29

Showing results (271-280 of 289) with videos related to

Sort By:
Pageof 29
The Journal of Clinical Endocrinology and Metabolism|November 20, 2012
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA InvestigatorsAnne-Paule Gimenez-Roqueplo, Aurore Caumont-Prim, Claire Houzard, et al.
EMBO Molecular Medicine|January 25, 2023
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotypeBérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar, et al.
Circulation|September 15, 2010
Composite cell sheets: a further step toward safe and effective myocardial regeneration by cardiac progenitors derived from embryonic stem cellsAlain Bel, Valérie Planat-Bernard, Atsuhiro Saito, et al.
Blood|March 16, 2025
The neutrophil antigen 3a/b polymorphism in SLC44A2 unexpectedly encodes Csa/Csb red cell antigensRomain Duval, Alissa Soudry, Jonathan De Oliveira Rios, et al.
Blood|March 25, 2021
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disordersRomain Duval, Gaël Nicolas, Alexandra Willemetz, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.
ISBT Science Series|November 3, 2017
International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetingsJ R Storry, L Castilho, Q Chen, et al.
Blood|December 12, 2019
Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregationSlim Azouzi, Mahmoud Mikdar, Patricia Hermand, et al.
Vox Sanguinis|November 14, 2018
International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetingsJill R Storry, Frederik Banch Clausen, Lilian Castilho, et al.
Pageof 29