Results 211 to 220 of about 79,824 (366)

Genetics of Atopy: A Study on 279 Asthmatic Children [PDF]

open access: bronze, 1999
A Cantani, D Gagliesi, A Di Rienzo
openalex   +1 more source

Prevalence of atopy, eosinophilia, and IgE elevation in IgG4‐related disease

open access: yesAllergy. European Journal of Allergy and Clinical Immunology, 2014
E. Della Torre   +5 more
semanticscholar   +1 more source

Type 2 gene expression signature in severe asthma associates with more advanced airway remodeling

open access: yesClinical and Translational Allergy, Volume 15, Issue 6, June 2025.
Abstract Background Asthma is a heterogeneous disease with various inflammatory subtypes, including the type‐2 (T2) endotype associated with airway eosinophilia. Severe asthma is linked to reduced ventilatory function due to airway structural changes.
Bogdan Jakiela   +12 more
wiley   +1 more source

Brief neonatal exposure to cows' milk and atopy [PDF]

open access: green, 1999
Giorgio Tamburlini   +2 more
openalex   +1 more source

Effects of early-life exposure to allergens and bacteria on recurrent wheeze and atopy in urban children.

open access: yesJournal of Allergy and Clinical Immunology, 2014
S. Lynch   +20 more
semanticscholar   +1 more source

Risk of asthma in individuals with eosinophilic esophagitis: Population‐based cohort study with sibling analyses

open access: yesClinical and Translational Allergy, Volume 15, Issue 6, June 2025.
Abstract Introduction There are limited data on the relationship between eosinophilic esophagitis (EoE) and asthma. We aimed to assess the risk of asthma in EoE patients compared with matched controls and siblings. Methods Through the ESPRESSO study, a Swedish nationwide population‐based histopathology cohort, we identified EoE patients diagnosed ...
Niki Mitselou   +5 more
wiley   +1 more source

Expanding the phenotypic and genetic landscape of congenital neutropenia through whole‐exome and genome sequencing

open access: yesHemaSphere, Volume 9, Issue 6, June 2025.
Abstract Congenital neutropenia (CN) comprises a heterogeneous group of rare genetic disorders. While some CN cases present only with neutropenia, others present with additional extra‐hematological manifestations. The most common cause of CN is variants in ELANE; however, approximately 30 other genes have been implicated.
Séverine Marti   +32 more
wiley   +1 more source

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