Zobrazeno 1 - 10
of 269
pro vyhledávání: '"Hanane Latrech"'
Publikováno v:
Diabetes Epidemiology and Management, Vol 16, Iss , Pp 100231- (2024)
Background: Diabetic ketoacidosis is a severe metabolic emergency often associated with the onset of Type 1 Diabetes Mellitus, with significant morbidity and mortality. Its incidence as the initial presentation of Type 1 Diabetes Mellitus varies wide
Externí odkaz:
https://doaj.org/article/74de82b9aba849eaa4a4cb3633a80272
Publikováno v:
Diabetes Epidemiology and Management, Vol 17, Iss , Pp 100237- (2025)
Background: Vitamin D is an essential component of healthy bones and its deficiency is widespread in obese patients. Through our study, we aimed to look into vitamin D status in obese and non-obese patients and determine its association with hyperten
Externí odkaz:
https://doaj.org/article/19c91ccab5514f0691eb0dfe847ae50b
Publikováno v:
Gynecological Endocrinology, Vol 40, Iss 1 (2024)
Introduction Polycystic ovary syndrome (PCOS) is a common hormonal disorder among women of reproductive age. The current study sought to assess vitamin D status in women with PCOS compared to the control group and to describe the association between
Externí odkaz:
https://doaj.org/article/ce3f8032995b49ce84dbbbc17b9518b2
Publikováno v:
Clinical Medicine Insights: Endocrinology and Diabetes, Vol 16 (2023)
Objectives: Our study aimed to compare the efficacy of transdermal dihydrotestosterone and testosterone enanthate in treating idiopathic micropenis. Patients and methods: It’s a comparative randomized study of 49 patients with idiopathic micropenis
Externí odkaz:
https://doaj.org/article/8e8e5ac9383f4633ab1010729aa04b4f
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2022)
Cushing’s disease or pituitary adrenocorticotropic hormone (ACTH)-dependent Cushing’s syndrome is considered a rare condition. It is caused by hypersecretion of the ACTH by a pituitary adenoma that ultimately induces endogenous hypercortisolism b
Externí odkaz:
https://doaj.org/article/e9dff54f1ae84d289811b61c4b1d42ee
Failure to Thrive Revealing a Pilomyxoid Astrocytoma: An Uncommon Case Report with Literature Review
Autor:
Salma Benyakhlef, Abir Tahri, Asmaa Khlifi, Hajar Abdelouahab, Kamaoui Imane, Fayçal Moufid, Siham Rouf, Hanane Latrech
Publikováno v:
Case Reports in Pediatrics, Vol 2021 (2021)
Pilomyxoid astrocytoma (PMA) is a freshly described figure of low-grade neoplasms encountered in early childhood. Nevertheless, its precise classification by the World Health Organization (WHO) is still debatable. Making an exact diagnosis relies on
Externí odkaz:
https://doaj.org/article/367311d017294b239dfaa2b607111f23
Publikováno v:
Case Reports in Endocrinology, Vol 2018 (2018)
Turner syndrome is a common sex chromosome disorder characterized by complete or partial absence of an X chromosome. The spectrum of its clinical features and cytogenetics are various. We report new chromosomal formula revealed by DSD and associated
Externí odkaz:
https://doaj.org/article/dd34dc78c9be4f43856415e1360016e2
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 24, Iss 2, Pp 392-402 (2013)
Numerous studies have shown that diabetic nephropathy (DNP) is associated with an elevated risk of progression toward end-stage renal disease (ESRD) as well as increased cardiovascular mortality. The majority of these studies are from the developed c
Externí odkaz:
https://doaj.org/article/4990245f8b3744b3afd3b39e6d8f1fdd
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:
Hanane Latrech, Ahmed Gaouzi
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 141 (2015)
Le déficit en 3ßéta Hydroxystéroïde Déshydrogénase (3 HSD) est un désordre autosomique récessif rare touchant les voies de synthèse de tous les stéroïdes actifs dans la surrénales et les gonades. Cliniquement, il inclut, à des degrés v
Externí odkaz:
https://doaj.org/article/95392d63f4834408b9233e4f82da32a9