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Arthritis Research & Therapy|July 11, 2009
Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseasesGhazi Chabchoub, Elif Uz, Abdellatif Maalej, et al.Chinese Neurosurgical Journal|June 30, 2023
Diagnosis and management of pituitary apoplexy: a Tunisian dataFaten Hadj Kacem, Oumeyma Trimeche, Imen Gargouri, et al.The Journal of Steroid Biochemistry and Molecular Biology|December 23, 2022
Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian populationBochra Ben Rhouma, Manuel Kley, Fakhri Kallabi, et al.Journal of Assisted Reproduction and Genetics|May 11, 2019
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadismMariam Moalla, Faten Hadj Kacem, Abdullah Fahad Al-Mutery, et al.European Journal of Medical Genetics|August 16, 2016
Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndromeAmine Chakroun, Mariem Ben Said, Amine Ennouri, et al.La Tunisie Medicale|March 25, 2026
Quality of life and Eating disorders in women with Polycystic Ovary SyndromeMouna Elleuch, Yesmine Elloumi, Imen Turki, et al.Endocrinology, Diabetes & Metabolism Case Reports|May 25, 2023
Insulinoma with equivocal imagingWafa Belabed, Fatma Mnif, Abdel Mouhaymen Missaoui, et al.European Journal of Pediatrics|May 14, 2015
Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effectNoura Bougacha-Elleuch, Nadia Charfi, Nabil Miled, et al.The American Journal of the Medical Sciences|April 23, 2023
Characteristics of adult-onset auto-immune type 1 diabetesFaten Hadj Kacem, Ameni Jerbi, Bibi Twaheerah Allymamod, et al.Pageof 7