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A nationwide survey of hospital-based thalassemia patients and standards of care and a preliminary assessment of the national prevention program in Sri Lanka.
PLoS One. 2019 Aug 16;14(8):e0220852. doi: 10.1371/journal.pone.0220852. eCollection 2019.
PLoS One. 2019.
PMID: 31419232
Free PMC article.
GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child - a case report.
Dayasiri KC, Suraweera N, Nawarathne D, Senanayake UE, Dayanath BKTP, Jasinge E, Weerasekara K.
Dayasiri KC, et al. Among authors: weerasekara k.
BMC Pediatr. 2019 Jun 15;19(1):199. doi: 10.1186/s12887-019-1580-x.
BMC Pediatr. 2019.
PMID: 31202265
Free PMC article.
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A novel mutation in ACADVL causing very long-chain acyl-coenzyme-A dehydrogenase deficiency in a South Asian pediatric patient: a case report and review of the literature.
Arunath V, Liyanarachchi MS, Gajealan S, Jasinge E, Weerasekara K, Moheb LA.
Arunath V, et al. Among authors: weerasekara k.
J Med Case Rep. 2021 Sep 1;15(1):441. doi: 10.1186/s13256-021-03013-y.
J Med Case Rep. 2021.
PMID: 34465376
Free PMC article.
Review.
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Van Wyk-Grumbach syndrome and oligosyndactyly in a 6-year-old girl: a case report.
Egodawaththe NS, Seneviratne SN, Gunasekara S, Amarasekara SM, Weerasekara K.
Egodawaththe NS, et al. Among authors: weerasekara k.
J Med Case Rep. 2020 Sep 16;14(1):166. doi: 10.1186/s13256-020-02472-z.
J Med Case Rep. 2020.
PMID: 32933589
Free PMC article.
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Two cases of mycetoma.
Ratnaike VT, Yoganathan M, Suntharalingam M, Athukorale DN, Weerasekara K.
Ratnaike VT, et al. Among authors: weerasekara k.
Ceylon Med J. 1969 Mar;14(1):32-4.
Ceylon Med J. 1969.
PMID: 5802507
No abstract available.
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