Results 111 to 120 of about 646 (169)

Effect of DNA methylation on inhibitor development in people with hemophilia A treated with FVIII concentrates. [PDF]

Res Pract Thromb Haemost
Chand H, Hassan S, Cairo A, Palla R, Peyvandi F, Survey of Inhibitors in Plasma-Product Exposed Toddlers Study Group.   +5 more
europepmc   +1 more source

Hemofilia A adquirida Acquired hemophilia A

Revista Cubana de Hematología, Inmunología y Hemoterapia, 2010
La hemofilia A adquirida (HAA) es un trastorno hemorrágico poco frecuente caracterizado por la presencia de autoanticuerpos contra el factor VIII (FVIII) circulante. Aproximadamente en la mitad de los casos se ha observado un grupo heterogéneo de procesos patológicos que incluyen, entre otros, enfermedades autoinmunes y malignas y durante el embarazo ...
openaire   +1 more source

Real-World Data on the Effectiveness and Safety of wilate for the Treatment of von Willebrand Disease. [PDF]

TH Open, 2021
Sholzberg M, Khair K, Yaish H, Rodgers G, Cruz MS, Mejía CM, Čermáková Z, Matino D, Teitel J, Barrie A, Werner S, Prondzinski MVD.   +11 more
europepmc   +1 more source

Hemofilias: uma abordagem atualizada

, 2015
Hemophilia A and B are the most common deficiencies of coagulation factors and are defined by the absence or decreased levels of FVIII and FIX, respectively. They are a result of the gene mutations of FVIII and FIX and are characterized by their sex-linked inheritance.
openaire   +1 more source

Hemophilic Pseudotumor of the Maxilla Secondary to Endodontic Treatment: Case Report and Systematic Review. [PDF]

Dent J (Basel)
Quiroz-Gomez JR, Roa-Encarnación CM, Puebla-Mora AG, Hernández-Morales A, Padilla-Rosas M, Nava-Villalba M.   +5 more
europepmc   +1 more source

Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy Carriers. [PDF]

Neurol Genet
Vigliano AP, Luce L, Pastor Rueda JM, Chaves H, Mesa L, Carcione M, Mazzanti C, Llames Massini C, Radic CP, Cejas C, Giliberto F.   +10 more
europepmc   +1 more source

Gene therapy as an innovative approach to the treatment of hemophilia B-a review. [PDF]

J Appl Genet
Wróblewska K, Bieszczad D, Popławska M, Ziętara KJ, Zajączkowska M, Filip A.   +5 more
europepmc   +1 more source

Hepatite C e hemofilia

, 2016
Virtually all hemophiliacs who underwent blood transfusions before 1992 were infected with HCV. In Portugal, 10-15% of these patients have hepatitis C. This viral infection is the leading cause of chronic liver disease in hemophiliacs, and the risk of death is 16.7 times higher than in the general population.
openaire   +1 more source