Results 161 to 170 of about 21,507,917 (245)

TRANSPLANTE HEPÁTICO NA HEMOFILIA A GRAVE: MANEJO PERIOPERATÓRIO E RESULTADO PÓS-TRANSPLANTE

Hematology, Transfusion and Cell Therapy
Tcpm Pedro, Chs Almeida, T. Fancicani, R. Pedro, Lms Malbouisson, A. Mendrone-Junior, C. Almeida-Neto   +6 more
semanticscholar   +1 more source

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

DOIS RELATOS DE CASO DE HEMOFILIA A ADQUIRIDA ATENDIDOS NO HC-FAMEMA EM 2023

Hematology, Transfusion and Cell Therapy
A. Melo, Alm Possetti, Gkm Grigoleto, Rns Antunes   +3 more
semanticscholar   +1 more source

PE-54 Educação física escolar e hemofilia: um relato de experiência sobre conscientização e inclusão

Jornal de Assistência Farmacêutica e Farmacoeconomia
Relato de experiência: A hemofilia é uma doença genética e hemorrágica caracterizada pela deficiência dos fatores de coagulação VIII (hemofilia A) ou IX (hemofilia B), provocando sangramentos frequentes, especialmente nas articulações.
Cassiane Araujo Elias, Clara Avelino Alves Henrique, Victoria Regina Antonina Lisboa, Thays Teller Vasconcelos Lima, Francisco Paula Careta   +4 more
doaj  

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