Senarathne UD - Search Results

1

Biochemical, Genetic and Clinical Diagnostic Approaches to Autism-Associated Inherited Metabolic Disorders.

Senarathne UD, Indika NR, Jezela-Stanek A, Ciara E, Frye RE, Chen C, Stepien KM. Senarathne UD, et al. Genes (Basel). 2023 Mar 27;14(4):803. doi: 10.3390/genes14040803. Genes (Basel). 2023. PMID: 37107561 Free PMC article. Review.

2

The Rationale for Vitamin, Mineral, and Cofactor Treatment in the Precision Medical Care of Autism Spectrum Disorder.

Indika NR, Frye RE, Rossignol DA, Owens SC, Senarathne UD, Grabrucker AM, Perera R, Engelen MPKJ, Deutz NEP. Indika NR, et al. Among authors: senarathne ud. J Pers Med. 2023 Jan 29;13(2):252. doi: 10.3390/jpm13020252. J Pers Med. 2023. PMID: 36836486 Free PMC article. Review.

3

Abnormal Porphyrin Metabolism in Autism Spectrum Disorder and Therapeutic Implications.

Indika NR, Senarathne UD, Malvaso A, Darshana D, Owens SC, Mansouri B, Semenova Y, Bjørklund G. Indika NR, et al. Among authors: senarathne ud. Mol Neurobiol. 2023 Nov 30. doi: 10.1007/s12035-023-03722-z. Online ahead of print. Mol Neurobiol. 2023. PMID: 38032468 Review.

4

Non-specificity of symptoms in infantile-onset Pompe disease may delay the diagnosis and institution of treatment.

Senarathne UD, Jasinge E, Viknarajah Mohan S, Waidyanatha S. Senarathne UD, et al. BMJ Case Rep. 2022 Mar 9;15(3):e247312. doi: 10.1136/bcr-2021-247312. BMJ Case Rep. 2022. PMID: 35264382 Free PMC article.

5

Patient with respiratory distress, facial oedema and refractory hypokalaemia.

Senarathne UD, Dayanath BKTP, Punchihewa R, Gunasena B. Senarathne UD, et al. BMJ Case Rep. 2021 May 7;14(5):e240330. doi: 10.1136/bcr-2020-240330. BMJ Case Rep. 2021. PMID: 33962921 Free PMC article.

6

The establishment of a population-specific reference value for the ruler drop test for the clinical assessment of reaction time.

Rajapaksha S, Kitulwatte I, Senarathne U, Edirisinghe A, Perera P. Rajapaksha S, et al. J Forensic Leg Med. 2023 May;96:102525. doi: 10.1016/j.jflm.2023.102525. Epub 2023 Apr 21. J Forensic Leg Med. 2023. PMID: 37119545

7

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.

Rathnasiri A, Senarathne U, Arunath V, Hoole T, Kumarasiri I, Muthukumarana O, Jasinge E, Mettananda S. Rathnasiri A, et al. BMC Endocr Disord. 2021 Oct 24;21(1):214. doi: 10.1186/s12902-021-00876-6. BMC Endocr Disord. 2021. PMID: 34689766 Free PMC article.

8

Milky pleural effusion in a neonate and approach to investigating chylothorax.

Senarathne UD, Rodrigo R, Dayanath BKTP. Senarathne UD, et al. BMJ Case Rep. 2021 Sep 29;14(9):e245576. doi: 10.1136/bcr-2021-245576. BMJ Case Rep. 2021. PMID: 34588205 Free PMC article.

9

The role of legal medicine professionals in preventing pregnancy and sexually transmitted infections among female victims of sexual assault.

Yesodharan R, Kamath P, Renjith V, Krishnan NM, Senarathne UD, Sasidharan SK, Jose TT, Nayak VC. Yesodharan R, et al. Among authors: senarathne ud. Forensic Sci Med Pathol. 2023 Sep;19(3):440-451. doi: 10.1007/s12024-023-00578-6. Epub 2023 Mar 7. Forensic Sci Med Pathol. 2023. PMID: 36881378 Free PMC article. Review.

10

Injuries in the vulnerable road user fatalities; a study from Sri Lanka.

Edirisinghe PA, Kitulwatte ID, Senarathne UD. Edirisinghe PA, et al. Among authors: senarathne ud. J Forensic Leg Med. 2014 Oct;27:9-12. doi: 10.1016/j.jflm.2014.07.002. Epub 2014 Jul 25. J Forensic Leg Med. 2014. PMID: 25287792

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