Results 11 to 20 of about 101,532 (231)

2010 international consensus algorithm for the diagnosis, therapy and management of hereditary angioedema [PDF]

open access: yes, 2010
Background We published the Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor [C1-INH] deficiency) and updated this as Hereditary angioedema: a current state-of-the-art ...
S. Waserman   +251 more
core   +1 more source

Population screening for hereditary and familial cancer syndromes in Valka district of Latvia [PDF]

open access: yes, 2010
Background The growing possibilities of cancer prevention and treatment as well as the increasing knowledge about hereditary cancers require proper identification of the persons at risk.
Arnis Āboliņš   +26 more
core   +2 more sources

Pathophysiology of Hereditary Angioedema [PDF]

open access: yesPediatric Allergy, Immunology, and Pulmonology, 2014
The genetic deficiency of the C1 inhibitor is responsible for hereditary angioedema (HAE), which is a disease transmitted as an autosomal dominant trait. More than 200 point mutations in the C1 inhibitor gene have been found to be associated with HAE. Patients with this disease suffer from recurrent angioedema, which is mediated by bradykinin derived ...
S. Caccia, C. Suffritti, M. Cicardi
openaire   +2 more sources

Treatment of Hereditary Angioedema [PDF]

open access: yesJournal of Investigational Allergology and Clinical Immunology, 2021
Hereditary angioedema due to C1-esterase inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease. In the last decade, new drugs and new indications for old drugs have played a role in the management of C1-INH-HAE. This review examines current therapy for C1-INH-HAE and provides a brief summary of drugs that are under development ...
openaire   +2 more sources

SEOM clinical guidelines in hereditary breast and ovarian cancer (2019) [PDF]

open access: yes, 2020
Mutations in BRCA1 and BRCA2 high penetrance genes account for most hereditary breast and ovarian cancer, although other new high-moderate penetrance genes included in multigene panels have increased the genetic diagnosis of hereditary breast and ovarian
González-Santiago, S   +20 more
core   +2 more sources

Hereditary angioedema (HAE) in children and adolescents : a consensus on therapeutic strategies [PDF]

open access: yes, 2012
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with intermittent episodes of potentially life-threatening angioedema ...
Martinez-Saguer, I   +35 more
core   +2 more sources

Optimum Use of Acute Treatments for Hereditary Angioedema: Evidence-Based Expert Consensus

open access: yesFrontiers in Medicine, 2018
Acute treatment of hereditary angioedema due to C1 inhibitor deficiency has become available in the last 10 years and has greatly improved patients’ quality of life.
Hilary Longhurst
doaj   +1 more source

WAO guideline for the management of hereditary angioedema [PDF]

open access: yes, 2012
Hereditary Angioedema (HAE) is a rare disease and for this reason proper diagnosis and appropriate therapy are often unknown or not available for physicians and other health care providers.
Ruby Pawankar   +39 more
core   +1 more source

Hospitalizations due to Angioedema without Urticaria in a Portuguese Center: Five Year Retrospective Study

open access: yesActa Médica Portuguesa, 2019
Introduction: Hospitalizations due to angioedema are important especially in debilitating or life-threatening situations. The aim of this study was to evaluate the frequency and etiology of angioedema without urticaria in hospital admissions.
Joana Cosme   +3 more
doaj   +1 more source

The Gabriel-Roiter measure for representation-finite hereditary algebras [PDF]

open access: yes, 2006
Chen B. The Gabriel-Roiter measure for representation-finite hereditary algebras.
Chen, Bo
core   +1 more source

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