Results 111 to 120 of about 20,403 (220)

Natural History of Hyperphagia in Patients with Pseudohypoparathyroidism

open access: yes
Background/Objectives: Pseudohypoparathyroidism (PHP) is a group of genetic disorders characterized by end-organ resistance to multiple hormones, short stature, brachydactyly, subcutaneous ossifications, obesity, and developmental delays.
Ashley H. Shoemaker, Jaclyn Tamaroff
core   +1 more source

Loss of Drosophila UBE3A phenocopies Piezo dysfunction and drives hyperphagic feeding in Drosophila

open access: yesFly
Angelman syndrome (AS) is a rare neurogenetic disorder characterized by developmental delay, speech impairment, ataxia, epilepsy, and in some cases hyperphagic feeding behavior.
Benjamin Geier   +3 more
doaj   +1 more source

Prader-Willi Syndrome and the Role of Ghrelin in the Development of Hyperphagia : -A Literature Review

open access: yes
Abstrakt Bakgrund: Prader Willis syndrom (PWS) är ett sällsynt syndrom som orsakas av en avvikelse på kromosom 15. Individer med PWS genomgår en övergång från ett anorektiskt stadie under första levnadsåret till att senare drabbas av en överdriven ...
Wengelin, Marlene
core   +3 more sources

Managing Hyperphagia, Obesity, and Hyperglycemia in Prader-Willi Syndrome: A Meta-Analysis of GLP-1 Agonists and SGLT2 Inhibitors

open access: yesInternational Journal of Medical Students
Background: Prader-Willi Syndrome (PWS) is a genetic disorder caused by a deletion, mutation, or imprinting error of the paternal 15q11-13 region or by maternal uniparental disomy of chromosome 15.
Saumika Mulluri
doaj   +1 more source

Improving the diagnosis of hyperphagia in melanocortin‐4 receptor pathway diseases

open access: yes
Characteristics of hyperphagia include heightened and prolonged hunger, longer time to satiation, shorter duration of satiety, severe preoccupation with food (i.e., hyperphagic drive), abnormal food-seeking behaviors, and distress or functional ...
Haqq, Andrea   +14 more
core   +1 more source

Kleine-Levin Syndorme: aetiology and pathogenesis, symptoms, diagnosis and treatment

open access: yesJournal of Education, Health and Sport, 2018
AIM: The aim of the study is to present the aetiology, pathogenesis, symptoms, diagnosis and treatment of Kleine-Levin syndrome (KLS). VIEW: Kleine-Levin syndrome is an extremely rare disease entity that consists of attacks of hypersomnia, cognitive and
Kamila Tuzim   +4 more
doaj  

Participação de a-adrenoceptores do núcleo mediano da rafe no controle da resposta ingestiva em ratos saciados [PDF]

open access: yes, 2014
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Biológicas, Programa de Pós-Graduação em Neurociências, Florianópolis, 2014.O presente estudo avaliou a participação de a-adrenoceptores do núcleo mediano da rafe (NMR ...
Levone, Brunno Rocha
core  

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