Senniappan S - Search Results

1

Klinefelter syndrome: going beyond the diagnosis.

Butler G, Srirangalingam U, Faithfull J, Sangster P, Senniappan S, Mitchell R. Butler G, et al. Among authors: senniappan s. Arch Dis Child. 2023 Mar;108(3):166-171. doi: 10.1136/archdischild-2020-320831. Epub 2022 Aug 10. Arch Dis Child. 2023. PMID: 35948402 Free PMC article. Review.

2

Variations in sex steroid priming for growth hormone stimulation testing in UK.

Frerichs C, Raymond L, Senniappan S. Frerichs C, et al. Among authors: senniappan s. Arch Dis Child. 2017 Mar;102(3):294. doi: 10.1136/archdischild-2016-311186. Epub 2016 Oct 27. Arch Dis Child. 2017. PMID: 27789462 No abstract available.

3

National consensus to develop core outcomes for the evaluation of complications from excess weight (CEW) clinics: results of a national Delphi process.

Stilwell PA, White B, Graham C, Rigby E, Shield JPH, Brandreth R, Solti S, Owen R, Kenny S; CEW Delphi Collaborators; CEW Delphi collaborators. Stilwell PA, et al. Arch Dis Child. 2023 Apr;108(4):296-299. doi: 10.1136/archdischild-2022-324550. Epub 2023 Jan 4. Arch Dis Child. 2023. PMID: 36599626

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

Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing.

Ghosh A, Schlecht H, Heptinstall LE, Bassett JK, Cartwright E, Bhaskar SS, Urquhart J, Broomfield A, Morris AA, Jameson E, Schwahn BC, Walter JH, Douzgou S, Murphy H, Hendriksz C, Sharma R, Wilcox G, Crushell E, Monavari AA, Martin R, Doolan A, Senniappan S, Ramsden SC, Jones SA, Banka S. Ghosh A, et al. Among authors: senniappan s. Arch Dis Child. 2017 Nov;102(11):1019-1029. doi: 10.1136/archdischild-2017-312738. Epub 2017 May 3. Arch Dis Child. 2017. PMID: 28468868

6

Mode of clinical presentation and delayed diagnosis of Turner syndrome: a single Centre UK study.

Apperley L, Das U, Ramakrishnan R, Dharmaraj P, Blair J, Didi M, Senniappan S. Apperley L, et al. Among authors: senniappan s. Int J Pediatr Endocrinol. 2018;2018:4. doi: 10.1186/s13633-018-0058-1. Epub 2018 Jun 26. Int J Pediatr Endocrinol. 2018. PMID: 29983717 Free PMC article.

7

Effect of Growth Hormone Therapy in Patients with Noonan Syndrome: A Retrospective Study.

Apperley LJ, Ramakrishnan R, Dharmaraj P, Das U, Didi M, Blair J, Senniappan S. Apperley LJ, et al. Among authors: senniappan s. Int J Endocrinol Metab. 2020 Oct 23;18(4):e107292. doi: 10.5812/ijem.107292. eCollection 2020 Oct. Int J Endocrinol Metab. 2020. PMID: 33613679 Free PMC article.

8

Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management.

Senniappan S, Shanti B, James C, Hussain K. Senniappan S, et al. J Inherit Metab Dis. 2012 Jul;35(4):589-601. doi: 10.1007/s10545-011-9441-2. Epub 2012 Jan 10. J Inherit Metab Dis. 2012. PMID: 22231386 Review.

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

45,X male - rare case of unbalanced translocation of Y chromosome to chromosome 2 presenting with developmental delay, learning difficulty and obesity.

Suntharesan J, Apperley L, Senniappan S. Suntharesan J, et al. Among authors: senniappan s. Endocrinol Diabetes Metab Case Rep. 2022 Nov 1;2022:22-0320. doi: 10.1530/EDM-22-0320. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 36515368 Free PMC article.

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