Omer Babiker - Search Results

Year	Number of Results
2015	1
2017	1
2018	1
2021	2
2022	3
2023	2
2024	1

1

Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post-partum haemorrhage (WOMAN): an international, randomised, double-blind, placebo-controlled trial.

WOMAN Trial Collaborators. WOMAN Trial Collaborators. Lancet. 2017 May 27;389(10084):2105-2116. doi: 10.1016/S0140-6736(17)30638-4. Epub 2017 Apr 26. Lancet. 2017. PMID: 28456509 Free PMC article. Clinical Trial.

2

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: babiker o. Sudan J Paediatr. 2021;21(1):53-60. doi: 10.24911/SJP.106-1588448825. Sudan J Paediatr. 2021. PMID: 33879944 Free PMC article.

3

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: babiker oo. 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

4

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: babiker o. Genes (Basel). 2022 Apr 8;13(4):657. doi: 10.3390/genes13040657. Genes (Basel). 2022. PMID: 35456463 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. Among authors: babiker oo. 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

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.

Zou M, Alzahrani AS, Al-Odaib A, Alqahtani MA, Babiker O, Al-Rijjal RA, BinEssa HA, Kattan WE, Al-Enezi AF, Al Qarni A, Al-Faham MSA, Baitei EY, Alsagheir A, Meyer BF, Shi Y. Zou M, et al. Among authors: babiker o. J Clin Endocrinol Metab. 2018 May 1;103(5):1889-1898. doi: 10.1210/jc.2017-02202. J Clin Endocrinol Metab. 2018. PMID: 29546359

7

Lessons Learned From COVID-19 Lockdown: An ASPED/MENA Study on Lifestyle Changes and Quality of Life During Ramadan Fasting in Children and Adolescents Living With Type 1 Diabetes.

Babiker A, Elbarbary NS, Alaqeel B, Al Noaim K, Al Yaarubi S, Al-Abdulrazzaq D, Al-Kandari H, Alkhayyat H, Odeh R, Babiker O, Abu-Libdeh A, Aljohani A, Al Abdul Salam N, Al-Juailla F, Masuadi E, Deeb A, Weissberg-Benchell J, Gregory AM, Hassanein M, Al Alwan I. Babiker A, et al. Among authors: babiker o. Clin Med Insights Endocrinol Diabetes. 2023 Oct 19;16:11795514231203907. doi: 10.1177/11795514231203907. eCollection 2023. Clin Med Insights Endocrinol Diabetes. 2023. PMID: 37867504 Free PMC article.

8

Impact of lockdown during COVID-19 on glycaemic control in children with type 1 diabetes mellitus following at diabetes clinic, Omdurman, Sudan.

Elrheima SA, Babiker OO. Elrheima SA, et al. Among authors: babiker oo. Sudan J Paediatr. 2023;23(2):163-170. doi: 10.24911/SJP.106-1670090324. Sudan J Paediatr. 2023. PMID: 38380404 Free PMC article.

9

Does vitamin D supplementation benefit patients with type 1 diabetes mellitus who are vitamin D deficient? A study was performed at the Sudan Childhood Diabetes Center from 2019 to 2022.

Suliman HA, Elkhawad AO, Babiker OO, Alhaj YM, Eltom KH, Elnour AA. Suliman HA, et al. Among authors: babiker oo. SAGE Open Med. 2024 May 6;12:20503121241242931. doi: 10.1177/20503121241242931. eCollection 2024. SAGE Open Med. 2024. PMID: 38711469 Free PMC article.

10

Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family.

Babiker O, Flanagan SE, Ellard S, Al Girim H, Hussain K, Senniappan S. Babiker O, et al. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1073-7. doi: 10.1515/jpem-2015-0033. J Pediatr Endocrinol Metab. 2015. PMID: 25915078

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