Results 121 to 130 of about 9,249 (245)

Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica

open access: yesRevista de Biología Tropical, 2004
Hemophilia Aand B are X-chromosome linked bleeding disorders caused by deficiency of the respective coagulation factor VIII and IX. Affected individuals develop a variable phenotype of hemorrhage caused by a broad range of mutations within the Factor ...
Lizbeth Salazar-Sánchez   +8 more
doaj  

Gene Therapy in Hemophilia: A Transformational Patient Experience. [PDF]

open access: yesJ Patient Exp, 2023
Rasul E   +7 more
europepmc   +1 more source

Factor XI Deficiency [PDF]

open access: yes, 2007
A deficiência de factor XI é uma doença hematológica rara na população em geral. Pode manifestar-se apenas como complicação hemorrágica no doente submetido a cirurgia electiva. Os autores descrevem o caso clínico de uma mulher de 59 anos, que apresenta
Alegria, A, Conde, P, Moniz, A
core  

Equidad en situaciones límite: acceso al tratamiento para personas con hemofilia [PDF]

open access: diamond, 2022
Andréa Carolina Lins de Góis   +3 more
openalex   +1 more source

Quality of life, self-reported outcomes and impact of education among people with moderate and severe hemophilia A: An integrated perspective from a Latin American country. [PDF]

open access: yesPLoS One, 2023
Torres L   +9 more
europepmc   +1 more source

Augusto Luiz Gonzaga [PDF]

open access: yes, 2009
RUIZ, Milton A.
core   +2 more sources

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