Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sudeshini Hewage"'
Autor:
Saumya Madushani Samarasinghe, Asanka Sudeshini Hewage, Rohan Chaminda Siriwardana, Kamani Hemamala Tennekoon, Madunil Anuk Niriella, Sumadee De Silva
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-14 (2023)
Abstract Background Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease showing a rising prevalence globally. Genetic predisposition plays a key role in the development and progression of the disease pathogenicity. Main
Externí odkaz:
https://doaj.org/article/be3e9ada715d47d9a7ec78ae9adc0c5f
Autor:
Saumya Madushani Samarasinghe, Asanka Sudeshini Hewage, Rohan Siriwardena, Kamani Hemamala Tennekoon, Madunil Anuk Niriella, Sumadee de Silva, Sameera Dhananjaya Viswakula
Background: Hepatocellular carcinoma (HCC) is becoming a challenging global health concern with Asian and African countries carrying the highest burden of it. The rising prevalence of non-alcoholic steatohepatitis (NASH) associated HCC is linked with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29f58f5b02cba521e19874db4cf9ed3b
https://doi.org/10.21203/rs.3.rs-2336549/v1
https://doi.org/10.21203/rs.3.rs-2336549/v1
Publikováno v:
The Ceylon medical journal. 65(4)
Introduction: Steroid hydroxylase deficiency due to CYP21A2 gene mutation is the most common cause of Congenital Adrenal Hyperplasia (CAH). Mutation spectrum in Sri Lankan CAH patients has not been investigated adequately. Objectives: This study atte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ddb72bac24a5880ad8dfb4a1240f6d
https://pubmed.ncbi.nlm.nih.gov/34821488
https://pubmed.ncbi.nlm.nih.gov/34821488
Autor:
Saumya Madushani Samarasinghe, Tharmini Sundralingam, Asanka Sudeshini Hewage, K.S.H. de Silva, Kamani Hemamala Tennekoon
Publikováno v:
Growth hormoneIGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society. 62
To identify and characterize a novel deletion at the LHX4 gene locus in a proband with growth hormone deficiency (GHD).Long range polymerase chain reaction (PCR) amplification was used to confirm the suspected deletion and to identify the rough locat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d05c57fdbf5194d0bf550dc4b80e23
https://pubmed.ncbi.nlm.nih.gov/34971854
https://pubmed.ncbi.nlm.nih.gov/34971854
Autor:
Sudeshini Hewage, Sumadee De Silva, Ruwandi Ranasinghe, Kamani H. Tennekoon, Tharmini Sundralingam, Shamya De Silva
Publikováno v:
Growth Hormone & IGF Research. :94-101
Objective Characterization of a deletion in the exon 1 and 5′ regulatory region of the GHRHR gene in a proband with isolated growth hormone deficiency. Methods Multiple ligation dependent probe amplification (MLPA) assay was carried out to confirm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20527134d27280bbef9a5f1457dee9dd
https://doi.org/10.1016/j.ghir.2018.10.005
https://doi.org/10.1016/j.ghir.2018.10.005