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Sudanese Journal of Paediatrics|August 6, 2016
Overview of diagnosis, management and outcome of congenital hypothyroidism: A call for a national screening programme in SudanAmir M I Babiker, Nasir A Al Jurayyan, Sarar H Mohamed, et al.Sudanese Journal of Paediatrics|February 21, 2024
Central precocious puberty in Sudan: 10 years' experience of paediatric endocrinology centresOlivia A Al-Hassan, Mary S Limbe, Justin Warner, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Clinical profile and aetiologies of delayed puberty: a 15 years' experience from a tertiary centre in SudanMarwa S Galal, Salwa A Musa, Omer O Babiker, et al.Sudanese Journal of Paediatrics|April 21, 2021
Aetiologies and clinical patterns of hypopituitarism in Sudanese childrenSamar S Hassan, Renson Mukhwana, Salwa Musa, et al.Molecular Genetics and Metabolism|December 5, 2003
Lack of mutations in CYP2D6 and CYP27 in patients with apparent deficiency of vitamin D 25-hydroxylaseChin Jia Lin, Andrea Dardis, Sujeewa D Wijesuriya, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 30, 2002
Adolescent rickets in Saudi Arabia: a rich and sunny countryMohamed A Abdullah, Hamad S Salhi, Lina A Bakry, et al.Thyroid : Official Journal of the American Thyroid Association|October 31, 2018
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese FamiliesYui Watanabe, Ryan J Bruellman, Reham S Ebrhim, et al.Thyroid : Official Journal of the American Thyroid Association|December 24, 2019
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital HypothyroidismRyan Bruellman, Yui Watanabe, Reham Shareef, et al.Journal of Surgical Case Reports|November 2, 2020
Unusual localizations of hydatid cysts: a rare case report from SyriaZain Douba, Judy A Sinno, Haya Jawish, et al.Gene|August 16, 2022
Clinical presentation and molecular genetic analysis of a Sudanese family with a novel mutation in the CYP2R1 geneAsmahan T Abdalla, Marijke Koedam, Sten L S Drop, et al.Pageof 4