Results 101 to 110 of about 647 (169)

Importancia del diagnóstico de portadoras en familias con antecedentes de hemofilia

open access: yesRevista Cubana de Hematología, Inmunología y Hemoterapia
La hemofilia es una enfermedad hemorrágica hereditaria ligada al cromosoma X que se presenta debido a mutaciones en los genes del factor VIII (hemofilia A) y el factor IX (hemofilia B), que ocasiona una disminución o deficiencia funcional de estas ...
Kalia Lavaut Sánchez
doaj  

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

open access: yesTH Open, 2021
Sholzberg M   +11 more
europepmc   +1 more source

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

open access: yesRes Pract Thromb Haemost
Chand H   +5 more
europepmc   +1 more source

The impact of improving haemophilia A management within the Spanish National Healthcare System: a social return on investment analysis. [PDF]

open access: yesBMC Health Serv Res, 2022
Soto I   +9 more
europepmc   +1 more source

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

open access: yesJornal 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   +4 more
doaj  

Hemofilia A adquirida Acquired hemophilia A

open access: yesRevista 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

Hemofilias: uma abordagem atualizada

open access: yes, 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]

open access: yesDent J (Basel)
Quiroz-Gomez JR   +5 more
europepmc   +1 more source

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

open access: yesNeurol Genet
Vigliano AP   +10 more
europepmc   +1 more source

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