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Dineshani Hettiarachchi
Dineshani Hettiarachchi
Department of Anatomy, Genetics and Biomedical Informatics Faculty of Medicine,University of Colombo
Verified email at anat.cmb.ac.lk
Title
Cited by
Cited by
Year
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
11182022
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
302021
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
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
62024
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
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
The Impact and Challenges of Medical Journalism: A Review
N Noordeen, D Hettiarachchi
Univ Col Rev 1 (1), 37-46, 2020
42020
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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