Results 131 to 140 of about 1,647,336 (269)

Influence of Weight Loss and Weight Regain on Adipose Tissue Inflammation. [PDF]

open access: yesArterioscler Thromb Vasc Biol
Caceres L   +3 more
europepmc   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann   +6 more
wiley   +1 more source

Metformin abuse and weight loss: A case report. [PDF]

open access: yesWorld J Clin Cases
AlKhateb B, Alkhateb O, Daaboul B.
europepmc   +1 more source

ABDOMINOPLASTY IN A WOMAN AFTER A SIGNIFICANT WEIGHT LOSS

open access: diamond, 2021
A. DAVLATOV, Hamza Dodariyon, G. AL OMER
openalex   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini   +13 more
wiley   +1 more source

Sustained Weight Loss With Combined LEAP2 and Semaglutide Treatment in Mice. [PDF]

open access: yesDiabetes
Holm SK   +12 more
europepmc   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

Endoscopic approach for the management of a gastrogastric fistula, eroded band, and outlet stenosis after a vertical banded gastroplasty

open access: yesVideoGIE
Patricia Ruiz-Cota, MD   +5 more
doaj   +1 more source

Giant ovarian cyst mimicking no-weight loss after sleeve gastrectomy. [PDF]

open access: yesJ Surg Case Rep
D'Amato G   +9 more
europepmc   +1 more source

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