D.R. BELAIR - RTMKB

HAEMOPHILIA AND COAGULOPATHIES

HÉMOPHILIE ET COAGULOPATHIES


A - Z

 

ADAMTS13 A Disintegrin and Metalloprotease with Metallopeptidase with ThromboSpondin type 1, motif 13 (von Willebrand factor cleaving protease)

AFH Association Française des Hémophiles

AHF AntiHemophilic Factor A

AHG AntiHemophilic Globulin

AHVH Association de l'hémophilie (BE)

ARAH Azerbaijan Republic Association of Hemophilia

ARAS Autosomal Recessive Alport Syndrome

AS Alport Syndrome

CHS Canadian Hemophilia Society

EHC European Hemophilia Consortium / Consortium européen de l'hémophilie

Haemophilia A Hémophilie A, maladie de Christmas Steven (maladie génétique rare, déficit en facteur VIII) - See PubMed Hemophilia A

Haemophilia B Hémophilie B (maladie génétique rare, chromosome X, déficit en facteur IX) - See PubMed Hemophilia B, See also Haemagglutination

HFA Haemophilia Foundation Australia

Inhibitors Inhibiteurs - See PubMed Factor VIII inhibitor, Factor IX inhibitor

MHA May-Hegglin Anomaly (hereditary macrothrombocytopenia) / Syndrome de May-Hegglin

MvW Maladie de von Willebrand (Idem vWD, coagulopathie héréditaire, chromosome 12)

NHF National Hemophilia Foundation (USA)

RHS Russian Hemophilia Society

SA Syndrome d'Alport

SHG-ASH Schweizerische Hämophilie-Gesellschaft - Association Suisse des Hémophiles

vWD von Willebrand Disease (Same as MvW)

vWF von Willebrand Factor - See PubMed vWF

WAS Wiskott-Aldrich Syndrome (hemorraghic familial nephritis) / Thrombopénie héréditaire d'Aldrich (néphrite hématurique familiale avec surdité)

WASp Wiskott-Aldrich Syndrome protein

WFH World Federation of Haemophilia

XLAS X linked Alport Syndrome


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D.R. BELAIR

Scientific & Technical writer

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