Senniappan S - Search Results

1

A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular Carcinoma.

Blackburn J, Giri D, Ciolka B, Gossan N, Didi M, Kokai G, Waghorn A, Jones M, Senniappan S. Blackburn J, et al. Among authors: senniappan s. Case Rep Genet. 2018 Oct 17;2018:1381730. doi: 10.1155/2018/1381730. eCollection 2018. Case Rep Genet. 2018. PMID: 30416831 Free PMC article.

2

Fluoxetine-Induced Hypoglycaemia in a Patient with Congenital Hyperinsulinism on Lanreotide Therapy.

Giri D, Price V, Yung Z, Didi M, Senniappan S. Giri D, et al. Among authors: senniappan s. J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):347-50. doi: 10.4274/jcrpe.2818. Epub 2016 Apr 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 27087264 Free PMC article.

3

Successful transition to sulfonylurea therapy in two Iraqi siblings with neonatal diabetes mellitus and iDEND syndrome due to ABCC8 mutation.

Ozsu E, Giri D, Seymen Karabulut G, Senniappan S. Ozsu E, et al. Among authors: senniappan s. J Pediatr Endocrinol Metab. 2016 Dec 1;29(12):1403-1406. doi: 10.1515/jpem-2016-0149. J Pediatr Endocrinol Metab. 2016. PMID: 27849623

4

Subcutaneous calcifications and hypothyroidism: Is there a missing link?

Giri D, Jayaram R, Senniappan S. Giri D, et al. Among authors: senniappan s. Arch Dis Child Educ Pract Ed. 2018 Apr;103(2):88-89. doi: 10.1136/archdischild-2016-311834. Epub 2017 Jan 30. Arch Dis Child Educ Pract Ed. 2018. PMID: 28137922 No abstract available.

5

A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome.

Dayal D, Giri D, Senniappan S. Dayal D, et al. Among authors: senniappan s. Ann Pediatr Endocrinol Metab. 2017 Mar;22(1):65-67. doi: 10.6065/apem.2017.22.1.65. Epub 2017 Mar 31. Ann Pediatr Endocrinol Metab. 2017. PMID: 28443262 Free PMC article.

6

Congenital hyperinsulinism and Poland syndrome in association with 10p13-14 duplication.

Giri D, Patil P, Hart R, Didi M, Senniappan S. Giri D, et al. Among authors: senniappan s. Endocrinol Diabetes Metab Case Rep. 2017 Mar 31;2017:16-0125. doi: 10.1530/EDM-16-0125. eCollection 2017. Endocrinol Diabetes Metab Case Rep. 2017. PMID: 28458900 Free PMC article.

7

Silent Crooke's cell corticotroph adenoma of the pituitary gland presenting as delayed puberty.

Giri D, Roncaroli F, Sinha A, Didi M, Senniappan S. Giri D, et al. Among authors: senniappan s. Endocrinol Diabetes Metab Case Rep. 2017 Mar 31;2017:16-0153. doi: 10.1530/EDM-16-0153. eCollection 2017. Endocrinol Diabetes Metab Case Rep. 2017. PMID: 28458905 Free PMC article.

8

Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency.

Giri D, Rigden D, Didi M, Peak M, McNamara P, Senniappan S. Giri D, et al. Among authors: senniappan s. Int J Pediatr Endocrinol. 2017;2017:8. doi: 10.1186/s13633-017-0047-9. Epub 2017 Aug 4. Int J Pediatr Endocrinol. 2017. PMID: 28785287 Free PMC article.

9

Testosterone Therapy Improves the First Year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty.

Giri D, Patil P, Blair J, Dharmaraj P, Ramakrishnan R, Das U, Didi M, Senniappan S. Giri D, et al. Among authors: senniappan s. Int J Endocrinol Metab. 2017 Mar 7;15(2):e42311. doi: 10.5812/ijem.42311. eCollection 2017 Apr. Int J Endocrinol Metab. 2017. PMID: 28848608 Free PMC article.

10

Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control.

Giri D, Pintus D, Burnside G, Ghatak A, Mehta F, Paul P, Senniappan S. Giri D, et al. Among authors: senniappan s. BMC Res Notes. 2017 Sep 7;10(1):465. doi: 10.1186/s13104-017-2794-3. BMC Res Notes. 2017. PMID: 28882195 Free PMC article.

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