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British Journal of Haematology|May 7, 2015
Progress in understanding the diagnosis and molecular genetics of macrothrombocytopeniasRemi Favier, Hana Raslova
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 19, 2015
Jacobsen syndrome: Advances in our knowledge of phenotype and genotypeRemi Favier, Natacha Akshoomoff, Sarah Mattson, et al.
Haematologica|November 5, 2020
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategyPaquita Nurden, Simon Stritt, Remi Favier, et al.
Pediatrics|August 14, 2013
First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopeniaRemi Favier, Joffrey Feriel, Marie Favier, et al.
A&A Practice|August 11, 2017
Eltrombopag to Treat Thrombocytopenia During Last Month of Pregnancy in a Woman With MYH9-Related Disease: A Case ReportRemi Favier, Celine De Carne, Elisabeth Elefant, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
The 11q terminal deletion disorder: a prospective study of 110 casesPaul D Grossfeld, Teresa Mattina, Zona Lai, et al.
Acta Haematologica|September 28, 2020
Eltrombopag for the Treatment of Severe Inherited ThrombocytopeniaKarim Abdelmoumen, Marc Fabre, Sophie Ducastelle-Lepretre, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 15, 2005
Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor XIkuko Isshiki, Remi Favier, Takanori Moriki, et al.
Thrombosis and Haemostasis|November 5, 2003
Paris-Trousseau syndrome : clinical, hematological, molecular data of ten new casesRemi Favier, Katayoun Jondeau, Patrice Boutard, et al.
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