Results 191 to 200 of about 148,802 (383)
Gastroesophageal reflux disease
In this review of gastroesophageal reflux disease (GERD), we discuss the different aspects of physiology and pathophysiology and then the approach to diagnosis outlining the advantages and disadvantages of each method. The last part of this review covers
Al-Karawi Mohammed
doaj
Digestive system disorders: gastroesophageal reflux disease [PDF]
David A. Katzka
openalex +1 more source
Phenotypes of Gastroesophageal Reflux Disease: Where Rome, Lyon, and Montreal Meet.
D. Katzka, J. Pandolfino, P. Kahrilas
semanticscholar +1 more source
Abstract Background The role of the gastric microbiome in the pathophysiology of gastritis beyond Helicobacter pylori (HP) infection is poorly understood and has remained unexplored in patients with obesity. The aim of this study was to analyse gastric mucosa‐associated microbiota in patients with obesity and nonatrophic chronic gastritis in the ...
José Ignacio Martínez‐Montoro+7 more
wiley +1 more source
Gastroesophageal reflux disease (GERD) treatment patterns and economic outcomes in a managed care population [PDF]
Joshua D. Hall
openalex +1 more source
MBOAT7 encephalopathy: Characterizing the neurology and epileptology
Abstract Objective Biallelic pathogenic MBOAT7 variants are associated with neurodevelopmental disorders, intellectual disability (ID), epilepsy, and neuropsychiatric disorders such as attention‐deficit/hyperactivity disorder and autism spectrum disorders. We aimed to characterize the epilepsy phenotype in a cohort of patients affected by this syndrome.
Sebastian Ortiz De la Rosa+28 more
wiley +1 more source
Editorial: Excluding Gastroesophageal Reflux Disease as the Cause of Chronic Cough
NULL AUTHOR_ID
openalex +1 more source
Chronic cough is associated with long breaks in esophageal peristaltic integrity on high-resolution manometry [PDF]
Bennett, Michael C.+5 more
core +2 more sources
Abstract The fibroblast growth factor 12 (FGF12) gene encodes a protein interacting with voltage‐gated sodium channels. Two variants, p.(Arg52His) and p.(Gly50Ser), have repeatedly been associated with developmental and epileptic encephalopathy‐47 (DEE47; Mendelian Inheritance in Man #617166) with poor outcome.
Clément Pierret+17 more
wiley +1 more source