Publications by authors named "Dominique Steschenko"

Claim this Profile
P
Previously misdiagnosed red cell membrane disorder and familial consequences.
Delphine Gérard, Sophie Bourin, Aurélie Phulpin, Véronique Picard, Dominique Steschenko

Br J Haematol· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience.
Ilhem Rahal, Claire Galambrun, Yves Bertrand, Nathalie Garnier, Catherine Paillard, Dominique Steschenko

Haematologica· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Oxidative stress-related infantile pyknocytosis with Heinz bodies.
Charlotte Stephan, Aurélie Phulpin, Dominique Steschenko, Jean-François Lesesve, Julien Perrin

Transfusion· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients.
Imane Agouti, Sylvie Cointe, Stéphane Robert, Coralie Judicone, Anderson Loundou, Dominique Steschenko

Br J Haematol· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
Aurélie Méneret, David Grabli, Christel Depienne, Cécile Gaudebout, Fabienne Picard, Dominique Steschenko

Neurology· July 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism.
Philippe Couarch, Santiago Vernia, Isabelle Gourfinkel-An, Gaëtan Lesca, Svetlana Gataullina, Dominique Steschenko

J Mol Med (Berl)· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females.
Christel Depienne, Oriane Trouillard, Delphine Bouteiller, Isabelle Gourfinkel-An, Karine Poirier, Dominique Steschenko

Hum Mutat· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
Lionel Arnaud, Carole Saison, Virginie Helias, Nicole Lucien, Dominique Steschenko

Am J Hum Genet· November 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease.
Gaetan Lesca, Nadia Boutry-Kryza, Bertrand de Toffol, Mathieu Milh, Dominique Steschenko

Epilepsia· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Complications and treatment of patients with β-thalassemia in France: results of the National Registry.
Isabelle Thuret, Corinne Pondarré, Anderson Loundou, Dominique Steschenko, Robert Girot

Haematologica· May 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis