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Autoimmune thyroid disease as a risk factor for angioedema in patients with chronic idiopathic urticaria: a case-control study
(Associação Paulista de Medicina (APM), 2012-01-01)
CONTEXTO E OBJETIVO: A associação de urticária crônica idiopática (UCI) com doença autoimune da tireoide (DAT) é relatada. Porém, não foram encontrados relatos se a DAT eleva o risco de angioedema, uma apresentação clínica ...
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
(Faculdade de Medicina / USP, 2011)
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the ...
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
(WILEY-BLACKWELL, 2011)
Background: Hereditary angioedema is an autosomal dominant disease characterized by episodes of subcutaneous and submucosal edema. It is caused by deficiency of the C1 inhibitor protein, leading to elevated levels of ...
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
(Brasil, 2011)
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the ...
The Diagnosis of Hereditary Angioedema: Family Caregivers’ Experiences
(SAGE Publications Inc., 2020)
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
(Wiley-Blackwell, 2011-10-01)
Background: Hereditary angioedema is an autosomal dominant disease characterized by episodes of subcutaneous and submucosal edema. It is caused by deficiency of the C1 inhibitor protein, leading to elevated levels of ...
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
(Wiley-Blackwell, 2011-10-01)
Background: Hereditary angioedema is an autosomal dominant disease characterized by episodes of subcutaneous and submucosal edema. It is caused by deficiency of the C1 inhibitor protein, leading to elevated levels of ...
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
(Hospital Clinicas, Univ São Paulo, 2011-01-01)
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the ...
Urticaria aguda y angioedema: etiología y características clínicas
(Instituto de Investigaciones en Ciencias de la Salud, 2007)
Dictamen Preliminar de Evaluación de Tecnología Sanitaria N° 030-DETS-IETSI-2022. Eficacia y seguridad de ecalantida en el tratamiento de los ataques agudos en pacientes con angioedema hereditario
(Seguro Social de Salud (EsSalud), 2022-08)
En este documento se plasma la evaluación de la eficacia y seguridad del uso del producto farmacéutico ecalantida en el tratamiento de los ataques agudos en pacientes con angioedema hereditario; cuyos resultados sustentaron ...