フォロー
Dineshani Hettiarachchi
Dineshani Hettiarachchi
Department of Anatomy, Genetics and Biomedical Informatics Faculty of Medicine,University of Colombo
確認したメール アドレス: anat.cmb.ac.lk
タイトル
引用先
引用先
Antibody tests for identification of current and past infection with SARS‐CoV‐2
T Fox, J Geppert, J Dinnes, K Scandrett, J Bigio, G Sulis, D Hettiarachchi, ...
Cochrane database of Systematic reviews, 2022
11262022
Ethical responses to the COVID-19 pandemic—lessons from Sri Lanka
D Hettiarachchi, N Noordeen, C Gamakaranage, EARBD Somarathne, ...
Asian bioethics review 13, 225-233, 2021
332021
Systematic review on the rational use of amniotic membrane allografts in diabetic foot ulcer treatment
K Lakmal, O Basnayake, D Hettiarachchi
BMC surgery 21, 1-8, 2021
312021
Global age-sex-specific mortality, life expectancy, and population estimates in 204 countries and territories and 811 subnational locations, 1950–2021, and the impact of the …
AE Schumacher, HH Kyu, A Aali, C Abbafati, J Abbas, ...
The Lancet, 2024
242024
Optimizing amniotic membrane tissue banking protocols for ophthalmic use
D Hettiarachchi, VHW Dissanayake, HWW Goonasekera
Cell and tissue banking 17, 387-397, 2016
192016
Three novel variants in the arylsulfatase A (ARSA) gene in patients with metachromatic leukodystrophy (MLD)
D Hettiarachchi, VHW Dissanayake
BMC research notes 12, 1-4, 2019
112019
Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly
RSVHWD Dineshani Hettiaracchchi , Carine Bonnard, S. M. A. Jayawardana ...
BMC Medical Genetics 19 (125), 2018
112018
A Concise Review of Ketogenic Dietary Interventions in the Management of Rare Diseases
KLVHWD D. Hettiarachchi
Journal of Nutrition and Metabolism 2021 (Article ID 6685581), 1-12, 2021
92021
The New Normal of Medical Education - Challenges and Opportunities
South-East Asian Journal of Medical Education 14 (1), 2–5, 2020
9*2020
A novel mutation in the NAGLU gene associated with Sanfilippo syndrome type B (mucopolysaccharidosis III B)
D Hettiarachchi, N Nethikumara, BAPS Pathirana, K Weththasigha, ...
Clinical Case Reports 6 (6), 1051, 2018
92018
Undiagnosed diseases: needs and opportunities in 20 countries participating in the undiagnosed diseases network international
D Taruscio, M Salvatore, A Lumaka, C Carta, LL Cellai, G Ferrari, ...
Frontiers in Public Health 11, 1079601, 2023
82023
Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report
D Hettiarachchi, H Panchal, PS Lai, VHW Dissanayake
BMC Medical Genetics 21, 1-7, 2020
82020
Genetic determinants of syndactyly: perspectives on pathogenesis and diagnosis
A Cassim, D Hettiarachchi, VHW Dissanayake
Orphanet Journal of Rare Diseases 17 (1), 198, 2022
62022
Fifty liver transplants: a single centre experience of haemodynamic management in liver transplantation for cirrhosis [part 2]
The Sri Lanka Journal of Surgery 2021 (39(3)), 36-42, 2021
5*2021
The Delta variant of SARS-CoV-2: The current global scourge
VA Suranjith L Seneviratne, Pamodh Yasawardene, Dineshani Hettiarachchi ...
Sri Lankan Family Physician 36 (01), 17-25, 2021
5*2021
The Impact and Challenges of Medical Journalism: A Review
N Noordeen, D Hettiarachchi
Univ Col Rev 1 (1), 37-46, 2020
52020
A novel mutation in the EIF2B4 gene associated with leukoencephalopathy with vanishing white matter
D Hettiaracchchi, N Neththikumara, B Pathirana, A Padeniya, ...
Case Reports in Pediatrics 2018, 2018
52018
Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys
D Hettiarachchi, SMV Subasinghe, GG Anandagoda, H Panchal, PS Lai, ...
BMC Medical Genomics 15 (1), 82, 2022
42022
Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators
S Sciascia, D Roccatello, M Salvatore, C Carta, LL Cellai, G Ferrari, ...
Frontiers in Public Health 11, 1248260, 2023
32023
Correction to: Three novel variants in the arylsulfatase A (ARSA) gene in patients with metachromatic leukodystrophy (MLD)
D Hettiarachchi, VHW Dissanayake
BMC Research Notes 13, 2020
32020
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