Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Azzelarab, Meftah"'
Autor:
Hassani Chaymaa Alami, Abainou Lahousssaine, Ayoub Idrissi, Sanae Elhadri, Azzelarab Meftah, Hicham Baizri
Publikováno v:
Endocrine Abstracts.
Autor:
Hassani Chaymaa Alami, Ayoub Idrissi, Abainou Lahousssaine, Sanae Elhadri, Azzelarab Meftah, Hicham Baizri
Publikováno v:
Endocrine Abstracts.
Autor:
Hassani Chaymaa Alami, Ayoub Idrissi, Abainou Lahousssaine, Sanae Elhadri, Azzelarab Meftah, Hicham Baizri
Publikováno v:
Endocrine Abstracts.
Autor:
Fatima Akioud, Lhoussaine Abainou, Sanaa El-hadri, Ayoub Idrissi, Badia Belaabidia, Amine Azami, Azzelarab Meftah, Hicham Baizri
Publikováno v:
Indian Journal of Pathology and Oncology. 9:160-164
The Warthin-like variant is a rare and relatively unknown entity of papillary thyroid carcinoma. It is frequently associated with Hashimoto's thyroiditis. The cytologic diagnosis is difficult to evaluate because of the overlap of its findings with th
Autor:
Ayoub Idrissi, Hamza El Jadi, Azzelarab Meftah, Lahoussaine Abainou, Sanae Elhadri, Hicham Baïzri
Publikováno v:
Médecine des Maladies Métaboliques.
Autor:
Fatima Akioud, L houssaine Abainou, Sanaa El- Hadri, AyoubIdrissi, Azzelarab Meftah And Hicham Baizri
Necrobiosis lipoidica is a rare chronic granulomatous disease, often associated with diabetes mellitus. It is due to collagen degeneration with risk of ulceration. Necrobiosis lipoidica affects 0.3 to 1.2% of diabetic patients, mainly in the leg. Its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8166b0b1f2e09c44102243452611c993
Hepaticglycogenosis is an inherited abnormality characterized by excessive glycogen accumulation in hepatocytes.It is a hepatic complication of poorly controlled type 1 diabetes mellitus.It combines hepatomegaly, growth failure, and hepatic cytolysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3089734a1276122704e5cabf8c1a77f3
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
Publikováno v:
Annales d'Endocrinologie. 82:377
Introduction L’acromegalie est une endocrinopathie rare, en rapport avec l’hyperfonctionnement de l’axe somatotrope. Nous rapportons a travers cette observation un mode inhabituel de decouverte de l’acromegalie : l’anemie microcytaire. Obse
Publikováno v:
Annales d'Endocrinologie. 82:449
Introduction L’incidentalome parathyroidien designe un adenome parathyroidien, de decouverte fortuite lors d’une imagerie non motivee par l’exploration d’une pathologie parathyroidienne. Observation et discussion Nous rapportons le cas d’un