Results 61 to 70 of about 101,532 (231)

Maternal Prebiotic Supplementation Modifies Associations Between Intrapartum Antibiotics and Infant Allergy

open access: yesAllergy, EarlyView.
This study examined whether antibiotic use altered the risk of infant allergic disease within a maternal prebiotics supplementation trial. Intrapartum antibiotics were maternal antibiotics administered during childbirth, from the onset of labour or induction until 1‐h before delivery.
Summer V. M. Walker   +10 more
wiley   +1 more source

Public support for healthcare-mediated disclosure of hereditary cancer risk information : Results from a population-based survey in Sweden

open access: yes, 2020
Background: Targeted surveillance of at-risk individuals in families with increased risk of hereditary cancer is an effective prevention strategy if relatives are identified, informed and enrolled in screening programs.
Hellquist, BN   +37 more
core   +1 more source

Pathophysiology of Hereditary Angioedema [PDF]

open access: yesAmerican Journal of Rhinology & Allergy, 2011
Background Laryngeal angioedema may be associated with significant morbidity and even mortality. Because of the potential severity of attacks, both allergists and otolaryngologists must be knowledgeable about the recognition and treatment of laryngeal angioedema. This study describes the clinical characteristics
Bruce L, Zuraw, Sandra C, Christiansen
openaire   +2 more sources

Basophils in Immunity: Activation Pathways, Roles in Allergy and AllergoOncology and Application of the Basophil Activation Test

open access: yesAllergy, EarlyView.
ABSTRACT Basophils, the least abundant leukocytes, are increasingly recognised as potent immunomodulators. Upon activation, they rapidly release preformed granule‐associated mediators including histamine and lipid mediators such as LTC4, while cytokine production occurs over a longer timescale, contributing to downstream immune responses.
Jitesh Chauhan   +5 more
wiley   +1 more source

Unmet needs in the management of hereditary angioedema from the perspective of Brazilian patients

open access: yesWorld Allergy Organization Journal
Introduction: Hereditary angioedema (HAE) is a rare genetic disease characterized by recurrent, potentially life-threatening angioedema episodes. Despite its severity, including the risk of asphyxiation, HAE often remains underdiagnosed.
Pedro Giavina-Bianchi, MD, PhD   +4 more
doaj   +1 more source

Pediatric hereditary angioedema [PDF]

open access: yesPediatric Allergy and Immunology, 2013
Abstract Hereditary angioedema ( HAE ) is a lifelong illness characterized by recurrent swelling of the skin, intestinal tract, and, ominously, the upper airway. It is caused by inadequate activity of the protein C1‐inhibitor, with dysfunction in the kallikrein/bradykinin ...
openaire   +4 more sources

Updated EAACI Statement on Drug Hypersensitivity Skin Testing: Methodology and Non‐Irritative Concentrations

open access: yesAllergy, EarlyView.
ABSTRACT These updated EAACI guidelines aim to standardize skin testing methodologies for both immediate and non‐immediate drug hypersensitivity reactions. For immediate reactions, the optimal testing window is 4–6 weeks post‐reaction; whereas beyond 6 months, false‐negative results increase.
Annick Barbaud   +14 more
wiley   +1 more source

Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy [PDF]

open access: yes, 2004
Objective: To investigate auditory neural involvement in patients with Leber's hereditary optic neuropathy (LHON).Methods: Auditory assessment was undertaken in two patients with LHON.
Luxon, LM, Ceranic, B
core  

Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia [PDF]

open access: yes, 2005
Introduction The aim of the study is to evaluate the incidence and phenotype-genotype characteristics of hereditary breast and ovarian cancer syndromes in Latvia in order to develop the basis of clinical management for patients and their relatives ...
Gardovskis Janis   +21 more
core   +1 more source

ID280 MHT para profilaxia de crises de AEH tipo I e II para maiores de 2 anos de idade, gestantes ou lactantes

open access: yesJornal de Assistência Farmacêutica e Farmacoeconomia
Introdução O angioedema hereditário (AEH) por deficiência de C1-esterase é uma doença genética rara caracterizada pela deficiência ou disfunção do inibidor do C1-INH, também denominada tipo I ou tipo II.
Aramís Tupiná Alcântara de Moreira   +3 more
doaj   +1 more source

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