Vasanwala RF - Search Results

1

CANDLE syndrome: an extended clinical spectrum.

Wang H, Das L, Tan Hung Tiong J, Vasanwala RF, Arkachaisri T. Wang H, et al. Among authors: vasanwala rf. Rheumatology (Oxford). 2014 Nov;53(11):2119-20. doi: 10.1093/rheumatology/keu298. Epub 2014 Jul 26. Rheumatology (Oxford). 2014. PMID: 25065002 No abstract available.

2

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD) syndrome may have a hypothalamus-periaqueductal gray localization.

Chow C, Fortier MV, Das L, Menon AP, Vasanwala R, Lam JC, Ng ZM, Ling SR, Chan DW, Choong CT, Liew WK, Thomas T. Chow C, et al. Pediatr Neurol. 2015 May;52(5):521-5. doi: 10.1016/j.pediatrneurol.2014.11.019. Epub 2015 Feb 4. Pediatr Neurol. 2015. PMID: 25746964

3

Neonatal Diabetes in a Singapore Children's Hospital: Molecular Diagnoses of Four Cases.

Vasanwala RF, Lim SH, Ellard S, Yap F. Vasanwala RF, et al. Ann Acad Med Singap. 2014 Jun;43(6):314-9. Ann Acad Med Singap. 2014. PMID: 25028140 Free article.

4

Primary osteoporosis in children.

Tan LO, Lim SY, Vasanwala RF. Tan LO, et al. Among authors: vasanwala rf. BMJ Case Rep. 2017 Sep 1;2017:bcr2017220700. doi: 10.1136/bcr-2017-220700. BMJ Case Rep. 2017. PMID: 28866630 Free PMC article.

5

Cockayne Syndrome due to a maternally-inherited whole gene deletion of ERCC8 and a paternally-inherited ERCC8 exon 4 deletion.

Ting TW, Brett MS, Tan ES, Shen Y, Lee SP, Lim EC, Vasanwala RF, Lek N, Thomas T, Lim KW, Tan EC. Ting TW, et al. Among authors: vasanwala rf. Gene. 2015 Nov 10;572(2):274-8. doi: 10.1016/j.gene.2015.07.065. Epub 2015 Jul 22. Gene. 2015. PMID: 26210811

6

Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature.

Ting CY, Bhatia NS, Lim JY, Goh CJ, Vasanwala RF, Ong CC, Seow WT, Yeow VK, Ting TW, Ng IS, Jamuar SS. Ting CY, et al. Among authors: vasanwala rf. Eur J Med Genet. 2020 Feb;63(2):103652. doi: 10.1016/j.ejmg.2019.04.009. Epub 2019 Apr 13. Eur J Med Genet. 2020. PMID: 30986546 Review.

7

MIRAGE Syndrome Caused by a De Novo c.3406G>C (p. Glu1136Gln) Mutation in the SAMD9 Gene Presenting With Neonatal Adrenal Insufficiency and Recurrent Intussusception: A Case Report.

Chin X, Sreedharan AV, Tan EC, Wei H, Kuan JL, Ho CWW, Lam JCM, Ting TW, Vasanwala RF. Chin X, et al. Among authors: vasanwala rf. Front Endocrinol (Lausanne). 2021 Sep 29;12:742495. doi: 10.3389/fendo.2021.742495. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34659124 Free PMC article.

8

Patent ductus arteriosus in a late preterm neonate: think congenital hypopituitarism.

Kwan R, Vasanwala RF, Baral VR. Kwan R, et al. Among authors: vasanwala rf. BMJ Case Rep. 2022 Aug 18;15(8):e248188. doi: 10.1136/bcr-2021-248188. BMJ Case Rep. 2022. PMID: 35981751

9

Hypothyroidism presenting as torsion of a multicystic megaovary.

Vasanwala RF, Ho JM, Ong LY, Yap F. Vasanwala RF, et al. Arch Dis Child. 2012 Nov;97(11):972. doi: 10.1136/archdischild-2012-302244. Epub 2012 Jul 17. Arch Dis Child. 2012. PMID: 22806237 No abstract available.

10

Evaluation of risk factors associated with fragility fractures and recommendations to optimise bone health in children with long-term neurological condition.

Leow XYJ, Tan JTC, Yeo TH, Wong KPL, Mahadev A, Ang B, Vasanwala RF, Ng ZM. Leow XYJ, et al. Among authors: vasanwala rf. Singapore Med J. 2023 Sep;64(9):550-556. doi: 10.11622/smedj.2021124. Singapore Med J. 2023. PMID: 34600448 Free PMC article.

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