Results 261 to 270 of about 124,409 (322)

GASTROESOPHAGEAL REFLUX DISEASE AMONG CHILDREN AS A RISK FACTOR FOR ESOPHAGUS ADENOCARCINOMA

open access: green, 2006
Natalia V. Gerasimova   +4 more
openalex   +1 more source

Identification of Important and Relevant Functioning‐Based Outcomes for Persons With an Oral Health Condition From the Patient's Perspective

open access: yesJournal of Oral Rehabilitation, Volume 53, Issue 1, Page 211-235, January 2026.
Overview of the qualitative study “Identification of Important and Relevant Functioning‐Based Outcomes for Persons with an Oral Health Condition from the Patient's Perspective.” The study involved 36 adults with various oral health conditions and used focus groups and interviews analyzed thematically and linked to the ICF framework. Results covered all
C. Lenherr   +3 more
wiley   +1 more source

Global temporal trends and projections of gastroesophageal reflux disease prevalence: Age-period-cohort analysis 2021. [PDF]

open access: yesPLoS One
Xie F   +10 more
europepmc   +1 more source

Primary Human Tissue Models for Metabolic Dysfunction‐Associated Liver Disease ‐ toward Streamlining Drug Discovery with Patient‐Derived Assays

open access: yesAdvanced Biology, Volume 9, Issue 12, December 2025.
The review provides a critical up‐to‐date overview of the current landscape of human in vitro models for fatty liver disease, including spheroids, organoids, organ‐on‐a‐chip systems, bioprinted liver constructs and precision‐cut liver slices. Their utility for faithfully modeling different stages of MASLD and MASH are evaluated and their compatibility ...
Sonia Youhanna   +6 more
wiley   +1 more source

Antireflux mucosectomy in the management of gastroesophageal reflux disease with large hiatal hernia. [PDF]

open access: yesEndoscopy
Kure M   +6 more
europepmc   +1 more source

Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome (OMIM #619080)

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT This study presents the case of a child with multiple congenital anomalies, severe hypotonia, and profound bilateral sensorineural hearing loss. Functional bioenergetic assessments showed no significant mitochondrial respiratory defects, and riboflavin (Rf) status evaluation excluded a deficiency in Rf transporters as a cause of hearing loss ...
Piero Leone   +13 more
wiley   +1 more source

CLCN4 ‐Related Neurodevelopmental Condition: Characterization of Speech and Language Abilities

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Speech and language difficulties are a core feature of the CLCN4‐related neurodevelopmental condition, but these have not been well described. Here we systematically phenotype speech and language in 13 participants (10 female, aged 1 year 10 months–41 years 10 months) with pathogenic CLCN4 variants (12 missense de novo, 1 premature stop codon ...
Alexandra Garrett   +4 more
wiley   +1 more source

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