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Arteriosclerosis, Thrombosis, and Vascular Biology
|
April 22, 2017
Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin α<sub>IIb</sub>β<sub>3</sub> Activation
Eliane Berrou, Frédéric Adam, Marilyne Lebret, et al.
Plos One
|
December 10, 2015
Apoptotic Platelet Events Are Not Observed in Severe von Willebrand Disease-Type 2B Mutation p.V1316M
Eliane Berrou, Alexandre Kauskot, Frédéric Adam, et al.
Blood
|
July 26, 2014
A new form of macrothrombocytopenia induced by a germ-line mutation in the PRKACG gene
Vladimir T Manchev, Morgane Hilpert, Eliane Berrou, et al.
JCI Insight
|
October 14, 2016
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B
Alexandre Kauskot, Sonia Poirault-Chassac, Frédéric Adam, et al.
Blood
|
October 1, 2011
Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome
Paquita Nurden, Najet Debili, Isabelle Coupry, et al.
Blood
|
September 15, 2018
A mutation of the human
Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
American Journal of Human Genetics
|
March 4, 2014
Loss of α1β1 soluble guanylate cyclase, the major nitric oxide receptor, leads to moyamoya and achalasia
Dominique Hervé, Anne Philippi, Reda Belbouab, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
April 22, 2017
Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin α<sub>IIb</sub>β<sub>3</sub> Activation
Eliane Berrou, Frédéric Adam, Marilyne Lebret, et al.
Plos One
|
December 10, 2015
Apoptotic Platelet Events Are Not Observed in Severe von Willebrand Disease-Type 2B Mutation p.V1316M
Eliane Berrou, Alexandre Kauskot, Frédéric Adam, et al.
Blood
|
July 26, 2014
A new form of macrothrombocytopenia induced by a germ-line mutation in the PRKACG gene
Vladimir T Manchev, Morgane Hilpert, Eliane Berrou, et al.
JCI Insight
|
October 14, 2016
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B
Alexandre Kauskot, Sonia Poirault-Chassac, Frédéric Adam, et al.
Blood
|
October 1, 2011
Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome
Paquita Nurden, Najet Debili, Isabelle Coupry, et al.
Blood
|
September 15, 2018
A mutation of the human
Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
American Journal of Human Genetics
|
March 4, 2014
Loss of α1β1 soluble guanylate cyclase, the major nitric oxide receptor, leads to moyamoya and achalasia
Dominique Hervé, Anne Philippi, Reda Belbouab, et al.
Page
of 2