Shah P - Search Results

1

Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia.

McGlacken-Byrne SM, Mohammad JK, Conlon N, Gubaeva D, Siersbæk J, Schou AJ, Demirbilek H, Dastamani A, Houghton JAL, Brusgaard K, Melikyan M, Christesen H, Flanagan SE, Murphy NP, Shah P. McGlacken-Byrne SM, et al. Among authors: shah p. Eur J Endocrinol. 2022 Feb 22;186(4):417-427. doi: 10.1530/EJE-21-0897. Eur J Endocrinol. 2022. PMID: 35089870

2

Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia.

Senniappan S, Alexandrescu S, Tatevian N, Shah P, Arya V, Flanagan S, Ellard S, Rampling D, Ashworth M, Brown RE, Hussain K. Senniappan S, et al. Among authors: shah p. N Engl J Med. 2014 Mar 20;370(12):1131-7. doi: 10.1056/NEJMoa1310967. N Engl J Med. 2014. PMID: 24645945 Free article.

3

Chromosome 6q24 transient neonatal diabetes mellitus and protein sensitive hyperinsulinaemic hypoglycaemia.

Kalaivanan P, Arya VB, Shah P, Datta V, Flanagan SE, Mackay DJ, Ellard S, Senniappan S, Hussain K. Kalaivanan P, et al. Among authors: shah p. J Pediatr Endocrinol Metab. 2014 Nov;27(11-12):1065-9. doi: 10.1515/jpem-2014-0031. J Pediatr Endocrinol Metab. 2014. PMID: 24859512

4

Persistent hyperinsulinaemic hypoglycaemia in infancy.

Shah P, Demirbilek H, Hussain K. Shah P, et al. Semin Pediatr Surg. 2014 Apr;23(2):76-82. doi: 10.1053/j.sempedsurg.2014.03.005. Epub 2014 Mar 15. Semin Pediatr Surg. 2014. PMID: 24931352 Review.

5

Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy.

Demirbilek H, Shah P, Arya VB, Hinchey L, Flanagan SE, Ellard S, Hussain K. Demirbilek H, et al. Among authors: shah p. J Clin Endocrinol Metab. 2014 Oct;99(10):3660-7. doi: 10.1210/jc.2014-1866. Epub 2014 Jun 17. J Clin Endocrinol Metab. 2014. PMID: 24937539 Clinical Trial.

6

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: shah p. 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

7

Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.

Demirbilek H, Tahir S, Baran RT, Sherif M, Shah P, Ozbek MN, Hatipoglu N, Baran A, Arya VB, Hussain K. Demirbilek H, et al. Among authors: shah p. J Clin Endocrinol Metab. 2014 Dec;99(12):E2730-4. doi: 10.1210/jc.2014-2696. J Clin Endocrinol Metab. 2014. PMID: 25226297

8

Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation.

Shah P, Arya VB, Flanagan SE, Morgan K, Ellard S, Senniappan S, Hussain K. Shah P, et al. J Pediatr Endocrinol Metab. 2015 May;28(5-6):695-9. doi: 10.1515/jpem-2014-0371. J Pediatr Endocrinol Metab. 2015. PMID: 25518065

9

Postprandial hyperinsulinaemic hypoglycaemia secondary to a congenital portosystemic shunt.

Senniappan S, Pitt K, Shah P, Arya V, Jaiswal S, Haddad M, Hind J, Dhawan A, Davenport M, Hussain K. Senniappan S, et al. Among authors: shah p. Horm Res Paediatr. 2015;83(3):217-20. doi: 10.1159/000369014. Epub 2015 Jan 21. Horm Res Paediatr. 2015. PMID: 25613828

10

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia.

Roženková K, Güemes M, Shah P, Hussain K. Roženková K, et al. Among authors: shah p. J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):86-97. doi: 10.4274/jcrpe.1891. J Clin Res Pediatr Endocrinol. 2015. PMID: 26316429 Free PMC article. Review.

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