A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy.

Autor: Alqahtani MA; Department of Pediatrics, Aseer Central Hospital, Abha 62523, Saudi Arabia., Shati AA; Department of Child Health, College of Medicine, King Khalid University, Abha 61421, Saudi Arabia., Zou M; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia., Alsuheel AM; Department of Child Health, College of Medicine, King Khalid University, Abha 61421, Saudi Arabia., Alhayani AA; Department of Pediatrics, Aseer Central Hospital, Abha 62523, Saudi Arabia., Al-Qahtani SM; Department of Child Health, College of Medicine, King Khalid University, Abha 61421, Saudi Arabia., Gilban HM; Department of Pediatrics, Aseer Central Hospital, Abha 62523, Saudi Arabia., Meyer BF; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia., Shi Y; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.

Publikováno v: International journal of endocrinology [Int J Endocrinol] 2015; Vol. 2015, pp. 595164. Date of Electronic Publication: 2015 Jul 22.

Analysis of diarrhea episodes in children reported at a primary health care center in abha city in the year 2002.

Autor: Alshehri M; Assir Central Hospital, Abha, Saudi Arabia., Abdelmoneim I, Gilban HM

Publikováno v: Journal of family & community medicine [J Family Community Med] 2004 Jan; Vol. 11 (1), pp. 35-8.