Výsledky vyhledávání - "Halangoda, A."

Akademický článek

A neonate with metatropic dysplasia: A case report

Autor: M. C. Wettasinghe, N. Herath, E. Halangoda, N. D. Wickramasinghe

Publikováno v: Sri Lanka Journal of Medicine, Vol 32, Iss 1, Pp 51-54 (2023)

Metatropic dysplasia is a rare form of skeletal dysplasia in which characteristic clinical and imaging features are found at birth. The short limbs with relatively long trunk seen in the neonatal period change to short trunk in childhood due to progr

Externí odkaz: https://doaj.org/article/229a10c4a41c4a74b247522f1dd7a6c1

Zobrazit plný text záznamu

Altered mitochondrial dynamics in a novel cellular model of Leber Hereditary Optic Neuropathy (LHON)

Autor: Halangoda, Kolitha

Leber Hereditary Optic Neuropathy (LHON) is a disease that is caused by mutations in mitochondrial DNA resulting in vision loss due to retinal ganglion cell (RGC) degeneration. The exact pathophysiological mechanism causing RGC degeneration is poorly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______497::0c339620b206cdb5d79e3f31b3892805
http://summit.sfu.ca/item/18513

Zobrazit plný text záznamu

Akademický článek

Mutation frequency is reduced in the cerebellum of Big Blue ® mice overexpressing a human wild type SOD1 gene

Autor: Kunishige, Makoto, Hill, Kathleen A, Riemer, Amanda M, Farwell, Kelly D, Halangoda, Asanga, Heinmöller, Ernst, Moore, Stephen R, Turner, Dianna M, Sommer, Steve S ^*

Publikováno v: In Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis 2001 473(2):139-149

Zobrazit plný text záznamu

Akademický článek

The Big Blue® transgenic mouse mutation detection assay: the mutation pattern of sectored mutant plaques

Autor: Hill, Kathleen A ^a, Nishino, Hiroshi ^b, Buettner, Victoria L ^a, Halangoda, Asanga ^a, Li, Wenyan ^a, Sommer, Steve S ^{a, *}

Publikováno v: In Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis 1999 425(1):47-54

Zobrazit plný text záznamu

Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue-specific time courses of mutation frequency but similar mutation types

Autor: Kathleen A. Hill, Asanga Halangoda, Victoria L. Buettner, Steve S. Sommer, Jeffrey Longmate, William A. Scaringe, Stephen R. Moore, Makoto Kunishige

Publikováno v: Environmental and Molecular Mutagenesis. 43:110-120

Transgenic mouse mutation detection systems permit rapid determination of the frequency and type of mutations allowing direct examination of mutational markers for aging, neurodegeneration, and cancer. The Big Blue® transgenic mouse mutation detecti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a742d14852c7ccf8e37a1004e399e8e8
https://doi.org/10.1002/em.20004

Zobrazit plný text záznamu

Fever, confusion, acute kidney injury: is this atypical neuroleptic malignant syndrome following polypharmacy with clozapine and risperidone?

Autor: Scott Cherry, Daniel Wysoczanski, Dan Siskind, Priyangika Halangoda, Valeria Spivak

Publikováno v: Australasian Psychiatry. 24:602-603

Objective: Clozapine is the gold-standard antipsychotic medication for treatment-refractory schizophrenia (TRS). However, one potentially lethal side effect of clozapine, as with other antipsychotics, is neuroleptic malignant syndrome (NMS) which cou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baa041b7543264c4583135c6a1693e3f
https://doi.org/10.1177/1039856216649768

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání