Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hind Nafiaa"'
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 115 (2019)
Le syndrome de Prader Willi est une maladie génétique rare qui se manifeste par l'apparition d'une hyperphagie avec un risque d'obésité morbide, des difficultés d'apprentissage et des troubles du comportement, voire des troubles psychiatriques m
Externí odkaz:
https://doaj.org/article/c4d079098af44b20878e582f3a56782e
Publikováno v:
Scholars Journal of Medical Case Reports. 9:1096-1100
Introduction: The frequency of gastrointestinal manifestations in patients suffering with mood disorders, particularly bipolar disorders, pose specific physiopathological, etiological and therapeutic questions. We propose to address this issue throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::824e8aba199d4711033a7719dc9659c8
https://doi.org/10.36347/sjmcr.2021.v09i11.015
https://doi.org/10.36347/sjmcr.2021.v09i11.015
Publikováno v:
SAS Journal of Medicine. 7:436-442
Background: Individuals monitored for pulmonary disease represent a particularly vulnerable population to the Coronavirus. They present, prior to any COVID 19 exposure, a respiratory condition that could be complicated by a contamination with this vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c64024dd719b1fe67e6d77af84df66d
https://doi.org/10.36347/sasjm.2021.v07i09.010
https://doi.org/10.36347/sasjm.2021.v07i09.010
Publikováno v:
Pan African Medical Journal. 33
Prader Willi syndrome is a rare genetic disease. Symptoms include binge eating disorder associated with the risk of morbid obesity, learning difficulties and behavioral problems or even major psychiatric disorders. The purpose of this case study is t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7f6058121728bbc94a61634fb384cf3
https://doi.org/10.11604/pamj.2019.33.115.13726
https://doi.org/10.11604/pamj.2019.33.115.13726
