Al-Khawaga S - Search Results

1

A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency.

Al-Khawaga S, AlRayahi J, Khan F, Saraswathi S, Hasnah R, Haris B, Mohammed I, Abdelalim EM, Hussain K. Al-Khawaga S, et al. Front Pediatr. 2019 Jul 18;7:299. doi: 10.3389/fped.2019.00299. eCollection 2019. Front Pediatr. 2019. PMID: 31380330 Free PMC article.

2

Pathways governing development of stem cell-derived pancreatic β cells: lessons from embryogenesis.

Al-Khawaga S, Memon B, Butler AE, Taheri S, Abou-Samra AB, Abdelalim EM. Al-Khawaga S, et al. Biol Rev Camb Philos Soc. 2018 Feb;93(1):364-389. doi: 10.1111/brv.12349. Epub 2017 Jun 22. Biol Rev Camb Philos Soc. 2018. PMID: 28643455 Review.

3

Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1.

Memon B, Karam M, Al-Khawaga S, Abdelalim EM. Memon B, et al. Stem Cell Res Ther. 2018 Jan 23;9(1):15. doi: 10.1186/s13287-017-0759-z. Stem Cell Res Ther. 2018. PMID: 29361979 Free PMC article.

4

Diagnosis and management of hyperinsulinaemic hypoglycaemia.

Galcheva S, Al-Khawaga S, Hussain K. Galcheva S, et al. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):551-573. doi: 10.1016/j.beem.2018.05.014. Epub 2018 Jun 6. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086874 Review.

5

Correction to: Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1.

Memon B, Karam M, Al-Khawaga S, Abdelalim EM. Memon B, et al. Stem Cell Res Ther. 2018 Oct 7;9(1):262. doi: 10.1186/s13287-018-1002-2. Stem Cell Res Ther. 2018. PMID: 30292238 Free PMC article.

6

Diabetes Mellitus in a Patient With Lafora Disease: Possible Links With Pancreatic β-Cell Dysfunction and Insulin Resistance.

Nicolescu RC, Al-Khawaga S, Minassian BA, Hussain K. Nicolescu RC, et al. Front Pediatr. 2019 Jan 16;6:424. doi: 10.3389/fped.2018.00424. eCollection 2018. Front Pediatr. 2019. PMID: 30701169 Free PMC article.

7

The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism.

Galcheva S, Demirbilek H, Al-Khawaga S, Hussain K. Galcheva S, et al. Front Endocrinol (Lausanne). 2019 Feb 26;10:111. doi: 10.3389/fendo.2019.00111. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 30873120 Free PMC article. Review.

8

Ion Transporters, Channelopathies, and Glucose Disorders.

Demirbilek H, Galcheva S, Vuralli D, Al-Khawaga S, Hussain K. Demirbilek H, et al. Int J Mol Sci. 2019 May 27;20(10):2590. doi: 10.3390/ijms20102590. Int J Mol Sci. 2019. PMID: 31137773 Free PMC article. Review.

9

The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar.

Al-Khawaga S, Mohammed I, Saraswathi S, Haris B, Hasnah R, Saeed A, Almabrazi H, Syed N, Jithesh P, El Awwa A, Khalifa A, AlKhalaf F, Petrovski G, Abdelalim EM, Hussain K. Al-Khawaga S, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00753. doi: 10.1002/mgg3.753. Epub 2019 Aug 23. Mol Genet Genomic Med. 2019. PMID: 31441606 Free PMC article.

10

A Systematic Review of Childhood Diabetes Research in the Middle East Region.

Saraswathi S, Al-Khawaga S, Elkum N, Hussain K. Saraswathi S, et al. Front Endocrinol (Lausanne). 2019 Nov 19;10:805. doi: 10.3389/fendo.2019.00805. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31824422 Free PMC article.

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