Results 31 to 40 of about 8,881 (242)

Atención dental en pacientes diagnosticados con hemofilia grave a con presencia de inhibidores

open access: yesRevista Científica Especialidades Odontológicas UG, 2020
Enfermedad genética recesiva, cuyo gen está asociado con el cromosoma sexual X, caracterizada por la deficiencia de algunos factores de coagulación. La hemofilia A se clasifica como deficiencia de factor FVIII, hemofilia B (FIX), hemofilia C (FXI), que ...
Andrea Caiza Rennella   +3 more
doaj   +1 more source

Faktor Risiko Non-genetik Inhibitor Faktor VIII pada Pasien Hemofilia A

open access: yesSari Pediatri, 2016
Latar belakang. Terbentuknya inhibitor atau antibodi terhadap FVIII pada pasien hemofilia A menyebabkan FVIII eksogen yang diberikan tidak dapat berfungsi. Penyebab bersifat multifaktorial terdiri atas faktor genetik dan lingkungan.
Ahmad Saifudin   +2 more
doaj   +1 more source

Hemofilia: ejercicio y deporte [PDF]

open access: yes, 2011
El ejercicio físico y el deporte constituyen uno de los pilares básicos en el tratamiento de la hemofilia. Este trabajo describe un resumen de las características de la hemofilia y, a través de una exhaustiva revisión bibliográfica, se analiza la ...
Devís-Devís, José   +5 more
core   +1 more source

Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines

open access: yesHuman Mutation, Volume 41, Issue 12, Page 2058-2072, December 2020., 2020
Abstract In hemophilia A and B, analysis of the F8 and F9 gene variants enables carrier and prenatal diagnosis and prediction of risk for the development of inhibitors. The PedNet Registry collects clinical, genetic, and phenotypic data prospectively on more than 2000 children with hemophilia.
Nadine G. Andersson   +10 more
wiley   +1 more source

Hemofilia adquirida asociada a la infección por SARS-CoV2

open access: yesGalicia Clínica, 2022
SARS-CoV2 infection has been found to be associated with coagulopathy. Although thrombotic complications have been more frequently reported, hematologic autoimmune disorders have also been described.
Catarina Medeiros   +3 more
doaj   +1 more source

Determining meaningful health‐related quality‐of‐life improvement in persons with haemophilia A using the Haemophilia Quality of Life Questionnaire for Adults (Haem‐A‐QoL)

open access: yesHaemophilia, Volume 26, Issue 6, Page 1019-1030, November 2020., 2020
Abstract Introduction The Haem‐A‐QoL is frequently utilized in haemophilia clinical trials and captures relevant aspects of disease impact. Thresholds for some domains ‘Physical Health’ (PH), ‘Sports & Leisure’ (S&L) and ‘Total Score’ (TS) have previously been identified to benchmark the amount of change that is meaningful to patients, but not been ...
Sylvia von Mackensen   +5 more
wiley   +1 more source

Causas de Morte em Doentes com Hemofilia: Estudo Retrospectivo de 1979 a 2007, no Serviço de Imunohemoterapia do HSJ [PDF]

open access: yes, 1999
Neurokinin A (NKA) induces bronchoconstriction mediated by tachykinin NK2 receptors in animals and humans, and may be increased in asthma. Because beta(2)-adrenoceptor agonists are the most widely used bronchodilators in asthma, we investigated the ...
Ad F. Roffel   +13 more
core   +3 more sources

Hemofilia A adquirida: un diagnóstico de infarto

open access: yesRevista Colombiana de Cardiología, 2022
La hemofilia A adquirida es una entidad poco reportada y potencialmente fatal, que se asocia con la aparición de autoanticuerpos contra el factor VIII de la coagulación. Si bien puede estar subestimada, se calcula una incidencia aproximada de 1 a 1.5 casos por millón de habitantes con una mortalidad reportada entre el 9 y el 33%.
Sandra B. Amado-Garzón   +1 more
openaire   +2 more sources

Molecular characterization of hemophilia B patients in Colombia

open access: yesMolecular Genetics &Genomic Medicine, Volume 8, Issue 5, May 2020., 2020
This is the first molecular characterization of patients with Hemophilia B in Colombia. Using Sanger sequencing we found the patogenic variant in all patients. One large deletion of exon 3 and 4 hasn't been reported previously in international databases.
Yolima A. Parrado Jara   +3 more
wiley   +1 more source

ESTUDO DA ADESÃO AO TRATAMENTO PROFILÁTICO DOS PACIENTES COM HEMOFILIA, SEM INIBIDOR, ATENDIDOS EM CENTRO DE REFERÊNCIA DO CEARÁ

open access: yesHematology, Transfusion and Cell Therapy, 2023
A hemofilia hereditária, considerada uma doença rara, é uma coagulopatia ligada ao cromossomo X que se caracteriza pela ausência ou deficiência do Fator VIII na Hemofilia A e do Fator IX na Hemofilia B.
NM Beserra   +6 more
doaj   +1 more source

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