Nessa A - Search Results

1

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.

Rozenkova K, Malikova J, Nessa A, Dusatkova L, Bjørkhaug L, Obermannova B, Dusatkova P, Kytnarova J, Aukrust I, Najmi LA, Rypackova B, Sumnik Z, Lebl J, Njølstad PR, Hussain K, Pruhova S. Rozenkova K, et al. Among authors: nessa a. J Clin Endocrinol Metab. 2015 Dec;100(12):E1540-9. doi: 10.1210/jc.2015-2763. Epub 2015 Oct 2. J Clin Endocrinol Metab. 2015. PMID: 26431509

2

Molecular mechanisms of congenital hyperinsulinism.

Rahman SA, Nessa A, Hussain K. Rahman SA, et al. Among authors: nessa a. J Mol Endocrinol. 2015 Apr;54(2):R119-29. doi: 10.1530/JME-15-0016. Epub 2015 Mar 2. J Mol Endocrinol. 2015. PMID: 25733449 Review.

3

Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8.

Nessa A, Aziz QH, Thomas AM, Harmer SC, Tinker A, Hussain K. Nessa A, et al. Hum Mol Genet. 2015 Sep 15;24(18):5142-53. doi: 10.1093/hmg/ddv233. Epub 2015 Jun 19. Hum Mol Genet. 2015. PMID: 26092864

4

Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?

Rozenkova K, Nessa A, Obermannova B, Elblova L, Dusatkova P, Sumnik Z, Lebl J, Hussain K, Pruhova S. Rozenkova K, et al. Among authors: nessa a. J Pediatr Endocrinol Metab. 2017 Nov 27;30(12):1311-1315. doi: 10.1515/jpem-2017-0163. J Pediatr Endocrinol Metab. 2017. PMID: 29127764

5

Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.

Arya VB, Guemes M, Nessa A, Alam S, Shah P, Gilbert C, Senniappan S, Flanagan SE, Ellard S, Hussain K. Arya VB, et al. Among authors: nessa a. Eur J Endocrinol. 2014 Dec;171(6):685-95. doi: 10.1530/EJE-14-0353. Epub 2014 Sep 8. Eur J Endocrinol. 2014. PMID: 25201519

6

Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy.

Arya VB, Aziz Q, Nessa A, Tinker A, Hussain K. Arya VB, et al. Among authors: nessa a. Int J Pediatr Endocrinol. 2014;2014(1):24. doi: 10.1186/1687-9856-2014-24. Epub 2014 Dec 15. Int J Pediatr Endocrinol. 2014. PMID: 25584046 Free PMC article.

7

Hyperinsulinemic Hypoglycemia - The Molecular Mechanisms.

Nessa A, Rahman SA, Hussain K. Nessa A, et al. Front Endocrinol (Lausanne). 2016 Mar 31;7:29. doi: 10.3389/fendo.2016.00029. eCollection 2016. Front Endocrinol (Lausanne). 2016. PMID: 27065949 Free PMC article. Review.

8

Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia.

Nessa A, Kumaran A, Kirk R, Dalton A, Ismail D, Hussain K. Nessa A, et al. J Pediatr Endocrinol Metab. 2012;25(9-10):963-7. doi: 10.1515/jpem-2012-0165. J Pediatr Endocrinol Metab. 2012. PMID: 23426827

9

Severe resistance to weight gain, lack of stored triglycerides in adipose tissue, hypoglycaemia, and increased energy expenditure: a novel disorder of energy homeostasis.

Padidela R, Bennett K, Nessa A, Wells J, Aufieri R, James C, Smith VV, Brain C, Eaton S, Hussain K. Padidela R, et al. Among authors: nessa a. Horm Res Paediatr. 2012;77(4):261-8. doi: 10.1159/000337248. Epub 2012 Apr 26. Horm Res Paediatr. 2012. PMID: 22538517

10

Characterisation of older patients that require, but do not undergo, emergency laparotomy: a multicentre cohort study.

Price A, McLennan E, Knight SR, Reeves N, Chandler S, Boyle J, Pearce L, Moug SJ; ELF2 Study Group. Price A, et al. Br J Anaesth. 2024 Nov;133(5):973-982. doi: 10.1016/j.bja.2024.07.009. Epub 2024 Oct 4. Br J Anaesth. 2024. PMID: 39366845 Free article.

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