Remi Favier

Remi Favier

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Remi Favier

Remi Favier

Publications by authors named "Remi Favier"

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Assessment of Coagulation by Thromboelastography During Ongoing Postpartum Hemorrhage: A Retrospective Cohort Analysis.

Anesth Analg 2019 Sep 24. Epub 2019 Sep 24.

From the Anesthesiology Department, Hôpital Armand Trousseau, Assistance Publique Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1213/ANE.0000000000004422DOI Listing
September 2019

Progressive pigmented purpuric dermatosis and platelet delta storage pool deficiency in a child.

Pediatr Blood Cancer 2019 Jul 12;66(7):e27748. Epub 2019 Apr 12.

Service de Dermatologie, Hôpital René Dubos, Pontoise, France.

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http://dx.doi.org/10.1002/pbc.27748DOI Listing
July 2019

Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.

Haematologica 2019 Jun 13;104(6):1244-1255. Epub 2018 Dec 13.

Hematología Investigación, Instituto de Investigaciones Médicas "Dr. Alfredo Lanari", Facultad de Medicina, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Argentina

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http://dx.doi.org/10.3324/haematol.2018.188904DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545826PMC
June 2019

Disrupted filamin A/αβ interaction induces macrothrombocytopenia by increasing RhoA activity.

Blood 2019 Apr 2;133(16):1778-1788. Epub 2019 Jan 2.

Unité Mixte de Recherche (UMR) 1170, INSERM, Equipe Labelllisée Ligue Nationale Contre le Cancer, Gustave Roussy Cancer Campus, Université Paris-Sud, Université Paris-Saclay, Villejuif, France.

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http://dx.doi.org/10.1182/blood-2018-07-861427DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484462PMC
April 2019

Management of pregnancy for a patient with the new syndromic macrothrombocytopenia, DIAPH1-related disease.

Platelets 2018 Nov 9;29(7):737-738. Epub 2018 Jul 9.

c Service de Gynécologie-Obstétrique , Hôpital Pellegrin , Bordeaux , France.

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http://dx.doi.org/10.1080/09537104.2018.1492710DOI Listing
November 2018

Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α-granules.

Am J Hematol 2018 02 17;93(2):195-204. Epub 2017 Nov 17.

Institut Hospitalo-Universitaire de Rythmologie et de Modélisation Cardiaque, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1002/ajh.24958DOI Listing
February 2018

ACTN1-related Macrothrombocytopenia: A Novel Entity in the Progressing Field of Pediatric Thrombocytopenia.

J Pediatr Hematol Oncol 2017 11;39(8):e515-e518

*Department of pediatric Hematology and Oncology #Haematological Laboratory **French Reference Center for Inherited Platelet Disorders, Trousseau Hospital (AP-HP) ∥Department of Immunology and Hematology, Necker Hospital (AP-HP) ¶Haematological Laboratory, Robert Debré Hospital (AP-HP) †UPMC Univ Paris 06, UMR_S938, Sorbonne University, Paris ‡Department of General Pediatrics, Kremlin-Bicêtre Hospital (AP-HP), Kremlin-Bicêtre §Molecular Genetic Laboratory, INSERM, U1078, CHRU de Brest, Brest, France.

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http://Insights.ovid.com/crossref?an=00043426-201711000-0004
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http://dx.doi.org/10.1097/MPH.0000000000000885DOI Listing
November 2017

Identification of R102P Mutation in Hereditary Thrombocytosis.

Front Endocrinol (Lausanne) 2017 20;8:235. Epub 2017 Sep 20.

INSERM UMR1170, Gustave Roussy, Villejuif, France.

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http://dx.doi.org/10.3389/fendo.2017.00235DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611484PMC
September 2017

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

Blood 2016 06 15;127(23):2791-803. Epub 2016 Apr 15.

Department of Haematology, University of Cambridge, National Institute for Health Research BioResource-Rare Diseases, Cambridge University Hospitals, and National Health Service Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, United Kingdom;

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http://dx.doi.org/10.1182/blood-2015-12-688267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016734PMC
June 2016

A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.

Sci Transl Med 2016 Mar 2;8(328):328ra30. Epub 2016 Mar 2.

Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. National Health Service (NHS) Blood and Transplant, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. National Institute for Health Research (NIHR) BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

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http://dx.doi.org/10.1126/scitranslmed.aad7666DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903547PMC
March 2016

Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients.

Blood 2016 Jan 8;127(3):333-42. Epub 2015 Oct 8.

INSERM, Unité Mixte de Recherche (UMR) 1170, Gustave Roussy, Villejuif, France; Université Paris-Saclay, UMR1170, Gustave Roussy, Villejuif, France; UMR1170, Gustave Roussy, Villejuif, France; Consultation d'Hématologie-Immunologie, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1182/blood-2015-07-661983DOI Listing
January 2016

Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.

Br J Haematol 2015 Sep 5;170(5):626-39. Epub 2015 May 5.

Institut National de la Santé et de la Recherche Médicale, U1170, Equipe Labellisée Ligue Contre le Cancer, Villejuif, France.

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http://dx.doi.org/10.1111/bjh.13478DOI Listing
September 2015

Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.

Am J Med Genet C Semin Med Genet 2015 Sep 18;169(3):239-50. Epub 2015 Aug 18.

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http://dx.doi.org/10.1002/ajmg.c.31448DOI Listing
September 2015

Platelet glycoprotein VI binds to polymerized fibrin and promotes thrombin generation.

Blood 2015 Jul 14;126(5):683-91. Epub 2015 May 14.

Unité Mixte de Recherche S1148, INSERM, Paris, France; Université Paris Diderot, Paris, France; Centre Hospitalier Universitaire Bichat, Paris, France;

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http://dx.doi.org/10.1182/blood-2015-02-629717DOI Listing
July 2015

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.

Haematologica 2014 Aug 24;99(8):1387-94. Epub 2014 Apr 24.

Department of Medicine and Haematology, University Hospital of Verona, Verona, Italy.

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http://dx.doi.org/10.3324/haematol.2014.105924DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116839PMC
August 2014

Beware of hidden trains: simultaneous discovery of a MYH9-related disease and chronic lymphocytic leukaemia.

Br J Haematol 2014 Jan 10;164(2):162. Epub 2013 Oct 10.

Haematological Laboratory, Saint Antoine Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1111/bjh.12583DOI Listing
January 2014

Concomitant germ-line RUNX1 and acquired ASXL1 mutations in a T-cell acute lymphoblastic leukemia.

Eur J Haematol 2013 Sep 28;91(3):277-9. Epub 2013 Jun 28.

Faculté de Médecine, Aix-Marseille Université, Marseille, France; Département d'Hématologie, Institut Paoli-Calmettes, Marseille, France.

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http://dx.doi.org/10.1111/ejh.12147DOI Listing
September 2013

First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopenia.

Pediatrics 2013 Sep 12;132(3):e793-5. Epub 2013 Aug 12.

Assistance Publique-Hôpitaux de Paris, Armand Trousseau Children’s Hospital, French Reference Centre for Inherited Platelet Disorders, Paris, France.

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http://dx.doi.org/10.1542/peds.2012-3807DOI Listing
September 2013

MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.

Blood 2012 Sep 7;120(13):2719-22. Epub 2012 Jun 7.

Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche (UMR) 1009, Villejuif, France.

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http://dx.doi.org/10.1182/blood-2012-04-422352DOI Listing
September 2012

[Lupus anticoagulant-hypoprothrombinemia syndrome revealing systemic lupus in an 11-year old girl in a context of clinical and biological emergency].

Ann Biol Clin (Paris) 2012 Mar-Apr;70(2):226-30

Hôpitaux de Paris, Service d'hématologie biologique, Hôpital d'enfants Armand Trousseau, Paris.

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http://dx.doi.org/10.1684/abc.2012.0690DOI Listing
May 2012

The c.273+11dup genetic change in the WAS gene is a functionally neutral polymorphism.

Eur J Haematol 2011 Oct 11;87(4):366-71. Epub 2011 Aug 11.

Molecular Immunology and Innovative Biotherapies, INSERM U951, Généthon, Evry, France.

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http://dx.doi.org/10.1111/j.1600-0609.2011.01674.xDOI Listing
October 2011

Elevated circulating soluble thrombomodulin activity, tissue factor activity and circulating procoagulant phospholipids: new and useful markers for pre-eclampsia?

Eur J Obstet Gynecol Reprod Biol 2009 Sep 28;146(1):46-9. Epub 2009 Jun 28.

Diagnostica Stago, PAE Parispace 3, 125 Avenue Louis Roche, 92635 Gennevilliers Cedex, France.

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http://dx.doi.org/10.1016/j.ejogrb.2009.06.001DOI Listing
September 2009

P19INK4D links endomitotic arrest and megakaryocyte maturation and is regulated by AML-1.

Blood 2008 Apr 14;111(8):4081-91. Epub 2008 Feb 14.

Institut National de la Santé et de la Recherche Médicale U790, Villejuif, France.

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http://dx.doi.org/10.1182/blood-2007-09-113266DOI Listing
April 2008

Hb Calais [beta76(E20)Ala --> Pro]: a family study of a variant with decreased oxygen affinity.

Hemoglobin 2006 ;30(1):35-8

Service d'Hématologie Biologique, Hôpital Cochin, Paris, France.

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http://dx.doi.org/10.1080/03630260500454014DOI Listing
July 2006

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 X.

Blood Coagul Fibrinolysis 2005 Jan;16(1):9-16

Department of Internal Medicine, Division of Hematology, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

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http://dx.doi.org/10.1097/00001721-200501000-00002DOI Listing
January 2005

The 11q terminal deletion disorder: a prospective study of 110 cases.

Am J Med Genet A 2004 Aug;129A(1):51-61

Division of Pediatric Cardiology, Department of Pediatrics University of California, San Diego, CA 92123, USA.

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http://dx.doi.org/10.1002/ajmg.a.30090DOI Listing
August 2004

Paris-Trousseau syndrome : clinical, hematological, molecular data of ten new cases.

Thromb Haemost 2003 Nov;90(5):893-7

Service d'Hématologie Biologique, Hôpital d'enfants A. Trousseau, Paris, France.

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http://dx.doi.org/10.1160/TH03-02-0120DOI Listing
November 2003

Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity.

Br J Haematol 2003 Feb;120(4):627-32

Laboratoire Français du Fractionnement et des Biotechnologies, Centre Hospitalier de Bicêtre, Le Kremlin-Bicêtre, Hôpital A Trousseau, Paris, France.

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http://dx.doi.org/10.1046/j.1365-2141.2003.04163.xDOI Listing
February 2003