Zobrazeno 1 - 10
of 42
pro vyhledávání: '"M. Arambepola"'
Autor:
W. M. M. Arambepola, A. Jayasinghe
Publikováno v:
Sri Lanka Journal of Medicine, Vol 31, Iss 2, Pp 1-2 (2022)
No abstract available
Externí odkaz:
https://doaj.org/article/edfcf5dc671d4663be5f591882b14457
Publikováno v:
Sri Lanka Journal of Medicine, Vol 28, Iss 2, Pp 71-74 (2019)
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disorder. It is characterized by neonatal/ early onset non-autoimmune insulin dependent diabetes (permanent neonatal diabetes mellitus-PNDM) associated with spondyloepiphyseal dysplasia, t
Externí odkaz:
https://doaj.org/article/0a9d9fa4b44e42ffafd10fd6a229db1b
Autor:
Stephen Allen, Jahangir A. M. Khan, Anuja Premawardhena, Simon Dixon, M. Arambepola, Behrouz Nezafat Maldonado Maldonado, Savinda Arambepola, Hamish Reed-Embleton
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Pediatrics
BMC Pediatrics
Background Sri Lanka has a high prevalence of β-thalassaemia major. Clinical management is complex and long-term and includes regular blood transfusion and iron chelation therapy. The economic burden of β-thalassaemia for the Sri Lankan healthcare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95bd1fb65f002c520d8d69ef70619c34
http://link.springer.com/article/10.1186/s12887-020-02160-3
http://link.springer.com/article/10.1186/s12887-020-02160-3
Autor:
M. Arambepola, Sachith Mettananda, Anuja Premawardhena, Sanath P Lamabadusuriya, Nilam Jiffry, Windsor Perera, Stephen Allen, Nimal Katugaha, Vikita Mehta, Abirami Kirubarajan, Nancy F. Olivieri, Dayananda Bandara, Amir Sabouhanian, David C. Rees, Timothy G. St. Pierre, David J. Weatherall, Refai Cader, Dileepa Senajith Ediriweera, Robert C Yamashita, Shawn Khan, Shanthimala de Silva, Giulia Muraca, Chris Fisher, Angela Allen
Publikováno v:
The Lancet Global Health, Vol 10, Iss 1, Pp e134-e141 (2022)
BACKGROUND\ud Worldwide, haemoglobin E β-thalassaemia is the most common genotype of severe β-thalassaemia. The paucity of long-term data for this form of thalassaemia makes evidence-based management challenging. We did a long-term observational st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51c2e873cf8ae2fc1271d2409b83925f
Autor:
Udaya B. Nelumdeniya, Sanath P Lamabadusuriya, Shamila T De Silva, K.R.C. Pushpakumara, Anuja P Premawardhana, Udaya de Silva, Ishari Silva, Sujeewa D Amarasena, F Rajiyah, Nizri Hameed, K.P. Weerasekara, K K Hemantha, M. Arambepola, I Rifaya, M. Jansz, Nalika De Silva, Upul Navarathne, U Vaidyanatha, D K Shantha Kumara, RM Mudiyanse, V. Thirukumaran, Randima Dissanayaka, Wijesundara Dayanada Bandara, Devan Mendis, Sachith Mettananda, Nilam Jiffry, Angela Allen, Nancy F Oliveri, David J. Weatherall, M.A.C.M. Refai
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 8, p e0220852 (2019)
PLoS ONE, Vol 14, Iss 8, p e0220852 (2019)
ObjectivesOur aim was to describe the numbers and distribution of patients with different types of thalassemia and to assess the standards of care in all thalassemia treatment centers throughout Sri Lanka and the success of the ongoing prevention pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80b290059ae0cd3f3bc828e69f196f84
http://europepmc.org/articles/PMC6697367
http://europepmc.org/articles/PMC6697367
Publikováno v:
Sri Lanka Journal of Medicine, Vol 28, Iss 2, Pp 71-74 (2019)
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disorder. It is characterized by neonatal/ early onset non-autoimmune insulin dependent diabetes (permanent neonatal diabetes mellitus-PNDM) associated with spondyloepiphyseal dysplasia, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac147e7bf398c7b0e70794f0433d4f5
https://doi.org/10.4038/sljm.v28i2.126
https://doi.org/10.4038/sljm.v28i2.126
Autor:
Shanthimala de Silva, Julia Muraco, M. Arambepola, E. Vichinsky, Anuja Premawardhena, Chris Fisher, Laura Merson, David J. Weatherall, Angela Allen, Nancy F. Olivieri, Tim E. A. Peto
The thalassemias pose an increasing burden for health-care services in many Asian countries. In order to conserve rare resources, it is essential to determine the reasons for the remarkable phenotypic heterogeneity and natural history of these disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1e3bfd5c64adb7af530c112ef7f8f75
https://doi.org/10.1093/hmg/ddh250
https://doi.org/10.1093/hmg/ddh250
Autor:
Anuja Premawardhena, C A Fisher, Angela O’Donnell, Stephen Allen, David C. Rees, Nancy F. Olivieri, Tim E. A. Peto, David J. Weatherall, M. Arambepola
Severe forms of anemia in children in the developing countries may be characterized by different clinical manifestations at particular stages of development. Whether this reflects developmental changes in adaptation to anemia or other mechanisms is n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::701be879660da304074bee2df3f339c3
https://ora.ox.ac.uk/objects/uuid:aee0a59c-3269-4915-b7b6-91df69a7c055
https://ora.ox.ac.uk/objects/uuid:aee0a59c-3269-4915-b7b6-91df69a7c055
Autor:
Y.T. Liu, David J. Weatherall, Anuja Premawardhena, M. Arambepola, Chris Fisher, I.C. Verma, S.T. de Silva, John B. Clegg
Publikováno v:
Blood Cells, Molecules, and Diseases. 31:98-101
The promoter region of the UDP glucuronosyltransferase 1 gene (UGT1A1) contains a run of thymine-adenine (TA) repeats, usually six (TA)(6). As well as its relationship to Gilbert's syndrome, homozygosity for the extended sequence, (TA)(7) (TA)(7), ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d46ef0834d373786d37c53206791184d
https://doi.org/10.1016/s1079-9796(03)00071-8
https://doi.org/10.1016/s1079-9796(03)00071-8
Autor:
Chris Fisher, Vivekanandan Thayalsutha, David J. Weatherall, M. Arambepola, Nancy F. Olivieri, Tim E. A. Peto, Anuja Premawardhena, Angela Allen, Stephen Allen
Publikováno v:
Blood. 116(24)
Hemoglobin E β thalassemia is the commonest form of severe thalassemia in many Asian countries. Its remarkably variable clinical phenotype presents a major challenge to determining its most appropriate management. In particular, it is not clear why
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a7c93a5ede1314aa87b22dffaf8a349
http://ora.ox.ac.uk/objects/uuid:b4b0726d-b3cc-48f1-86f1-d794754b450a
http://ora.ox.ac.uk/objects/uuid:b4b0726d-b3cc-48f1-86f1-d794754b450a