Musa S - Search Results

1

Global perspective of psychosocial care of patients with differences of sex development from low-income countries.

Utari A, Silberkasten M, Musa S, Hassan S, Sharma R, Bramer W, van der Zwan YG, Drop SLS. Utari A, et al. Among authors: musa s. J Reprod Infant Psychol. 2024 Dec 18:1-19. doi: 10.1080/02646838.2024.2439926. Online ahead of print. J Reprod Infant Psychol. 2024. PMID: 39696731 Free article. Review.

2

Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports.

Ismail MM, Musa SA, Hassan SS, Abdullah MA. Ismail MM, et al. Among authors: musa sa. J Med Case Rep. 2023 Jun 2;17(1):244. doi: 10.1186/s13256-023-03927-9. J Med Case Rep. 2023. PMID: 37264371 Free PMC article.

3

Characterization of Hashimoto´s thyroiditis in Sudanese children: a cross-sectional study at Gaafar Ibnauf Hospital, Khartoum.

Fadlalbari GF, Musa SA, Hassan SS, Ibrahim AA, Abdullah MA. Fadlalbari GF, et al. Pan Afr Med J. 2023 Feb 14;44:86. doi: 10.11604/pamj.2023.44.86.35649. eCollection 2023. Pan Afr Med J. 2023. PMID: 37193101 Free PMC article.

4

Aetiologies and clinical patterns of hypopituitarism in Sudanese children.

Hassan SS, Mukhwana R, Musa S, Ibrahim AAB, Babiker O, Abdullah MA. Hassan SS, et al. Among authors: musa s. Sudan J Paediatr. 2021;21(1):53-60. doi: 10.24911/SJP.106-1588448825. Sudan J Paediatr. 2021. PMID: 33879944 Free PMC article.

5

Clinical profile, etiology, and diagnostic challenges of primary adrenal insufficiency in Sudanese children: 14-years' experience from a resource limited setting.

Musa SA, Hassan SS, Ahmed AI, Ngwiri T, Fadlalbari GF, Ibrahim AA, Babiker OO, Abdullah MA. Musa SA, et al. J Pediatr Endocrinol Metab. 2021 Oct 15;35(2):231-237. doi: 10.1515/jpem-2021-0545. Print 2022 Feb 23. J Pediatr Endocrinol Metab. 2021. PMID: 34653327

6

Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family.

Hassan SS, Kempers M, Lugtenberg D, Abdallah AT, Musa SA, Ibrahim AA, Abdullah MA. Hassan SS, et al. Pan Afr Med J. 2021 Oct 15;40:105. doi: 10.11604/pamj.2021.40.105.29527. eCollection 2021. Pan Afr Med J. 2021. PMID: 34887979 Free PMC article.

7

Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children.

Musa SA, Ibrahim AA, Hassan SS, Johnson MB, Basheer AT, Arabi AM, Abdullah MA. Musa SA, et al. Int J Pediatr Endocrinol. 2020 Nov 23;2020(1):21. doi: 10.1186/s13633-020-00091-5. Int J Pediatr Endocrinol. 2020. PMID: 33292488 Free PMC article.

8

A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees.

Hassan SS, Abdullah M, Trebusak Podkrajsek K, Musa S, Ibrahim A, Babiker O, Kovac J, Battelino T, Avbelj Stefanija M. Hassan SS, et al. Among authors: musa s. Genes (Basel). 2022 Apr 8;13(4):657. doi: 10.3390/genes13040657. Genes (Basel). 2022. PMID: 35456463 Free PMC article.

9

Clinical profile and aetiologies of delayed puberty: a 15 years' experience from a tertiary centre in Sudan.

Galal MS, Musa SA, Babiker OO, Hamdan HZ, Abdullah MA. Galal MS, et al. Among authors: musa sa. J Pediatr Endocrinol Metab. 2022 Jun 8;35(7):938-945. doi: 10.1515/jpem-2022-0243. Print 2022 Jul 26. J Pediatr Endocrinol Metab. 2022. PMID: 35671155

10

Central precocious puberty in Sudan: 10 years' experience of paediatric endocrinology centres.

Al-Hassan OA, Limbe MS, Warner J, Musa SA, Abdullah MA. Al-Hassan OA, et al. Among authors: musa sa. Sudan J Paediatr. 2023;23(2):145-152. doi: 10.24911/SJP.106-1652031727. Sudan J Paediatr. 2023. PMID: 38380412 Free PMC article.

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