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Diagnosis and management of hyperinsulinaemic hypoglycaemia.
Galcheva S, Al-Khawaga S, Hussain K. Galcheva S, et al. Among authors: hussain k. 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.
The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism.
Galcheva S, Demirbilek H, Al-Khawaga S, Hussain K. Galcheva S, et al. Among authors: hussain k. 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.
Ion Transporters, Channelopathies, and Glucose Disorders.
Demirbilek H, Galcheva S, Vuralli D, Al-Khawaga S, Hussain K. Demirbilek H, et al. Among authors: hussain k. 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.
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. Among authors: hussain k. 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.
Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype.
Mohammed I, Al-Khawaga S, Bohanna D, Shabani A, Khan F, Love DR, Nawaz Z, Hussain K. Mohammed I, et al. Among authors: hussain k. Mol Genet Genomic Med. 2020 Jun;8(6):e1086. doi: 10.1002/mgg3.1086. Epub 2020 Apr 11. Mol Genet Genomic Med. 2020. PMID: 32277595 Free PMC article.
943 results