Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Ghizlaine Belmejdoub"'
Publikováno v:
The Pan African Medical Journal, Vol 30, Iss 9 (2018)
Rickets are abnormalities of mineralization that can lead to bone fractures and deformities. Vitamin-resistant rickets is defined as any rickets not prevented by regular, early and prolonged administration of vitamin D and not cured by a sufficient t
Externí odkaz:
https://doaj.org/article/04c0350570d549a69effad5e3924883a
Autor:
Asmae Chadli, Siham El Aziz, Nawal El Ansari, Farida Ajdi, Mehdi Seqat, Hanane Latrech, Ghizlaine Belmejdoub
Publikováno v:
Therapeutic Advances in Endocrinology and Metabolism, Vol 7 (2016)
Objectives: The International Diabetes Mellitus Practice Study (IDMPS) is a 5-year survey documenting changes in diabetes treatment practices in developing countries. The primary objective of this survey was to assess the therapeutic management of ty
Externí odkaz:
https://doaj.org/article/f6c90c1f920c46a791602c4c415276bc
Autor:
Asmaa Yassine, Ahmed Anas Guerboub, Adil Arsalane, Abdelhamid Biyi, Souad El Moussaoui, Ghizlaine Belmejdoub
Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 290 (2015)
La tumeur brune est une entité clinique bénigne apparaissant comme une manifestation squelettique rare de l'hyperparathyroédie primaire. Il s'agit d'une cause inhabituelle de fractures pathologiques. Nous rapportons ici le cas clinique d'un patien
Externí odkaz:
https://doaj.org/article/8d3093319aaa46fb8eba9e21b59784d4
Publikováno v:
Clinics and Practice, Vol 5, Iss 1 (2015)
Autoimmune hypothyroidism is a common medical condition. Its revelation by thyrotrophic hyperplasia is an unusual and may be misdiagnosed as a pituitary adenoma. A 35-year-old man is referred to us for endocrinological assessment before surgery of a
Externí odkaz:
https://doaj.org/article/40988262751f4ad28374b0f1ff29d2ea
Autor:
Amal Moumen, Sanae Chakdoufi, Hamza El Jadi, Ouijdane Zammani, Cherif Abad El Asri, Ghizlaine Belmejdoub
Publikováno v:
Journal of Endocrinology and Metabolism. 11:52-55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df9b04800e3f0cc8869a1adf6a10d51e
https://doi.org/10.14740/jem730
https://doi.org/10.14740/jem730
Publikováno v:
Lifestyle and Epidemiology-The Double Burden of Poverty and Cardiovascular Diseases in African Populations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=intech______::3ef764c2f37c1ccf6000d14a56c2d26a
https://mts.intechopen.com/articles/show/title/type-2-diabetes-and-dysautonomy
https://mts.intechopen.com/articles/show/title/type-2-diabetes-and-dysautonomy
Autor:
Yassine Er-rahali, Amal Moumen, Souad Elmoussaoui, Ahmed Anass Guerboub, Ghizlaine Belmejdoub
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol. 39 No. 1 (2021)
Pan African Medical Journal; Vol. 39 No. 1 (2021)
L´hyperplasie macronodulaire bilatérale des surrénales (HMBS) est une cause rare de syndrome de Cushing d´origine surrénalienne, représentant moins de 1% des cas. Nous rapportons le cas d´un patient âgé de 48 ans, diabétique et hypertendu.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2993612fee2adf96bf67fe41410811a0
http://europepmc.org/articles/PMC8379406
http://europepmc.org/articles/PMC8379406
Publikováno v:
Pan African Medical Journal. 39
Bilateral macronodular adrenal hyperplasia (BMAH) is a rare cause of adrenal Cushing's syndrome, accounting for less than 1% of cases. We here report the case of a 48-year-old patient with diabetes and hypertension presenting with clinical signs of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72dca32685c8a3fb1f3d30cbfdee4f8e
https://doi.org/10.11604/pamj.2021.39.98.26041
https://doi.org/10.11604/pamj.2021.39.98.26041
Publikováno v:
Annales d'Endocrinologie. 82:475
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f6d5fc12e15ed3901323be9a9161a20
https://doi.org/10.1016/j.ando.2021.08.646
https://doi.org/10.1016/j.ando.2021.08.646
Publikováno v:
Annales d'Endocrinologie. 82:454
Introduction Le syndrome 46XX male est une maladie rare, caracterisee par un phenotype male avec un caryotype 46XX. Il est classe en deux groupes en fonction de la presence ou l’absence du gene SRY. Les organes genitaux externes et la masculinisati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50e5e76fdf0ade0757d982ea66d3e3e6
https://doi.org/10.1016/j.ando.2021.08.584
https://doi.org/10.1016/j.ando.2021.08.584