Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Emily Woods"'
2
Akademický článek
Sanitation practices and perceptions in Kakuma refugee camp, Kenya: Comparing the status quo with a novel service-based approach.
Autor: Raymond Nyoka, Andrew M Foote, Emily Woods, Hana Lokey, Ciara E O'Reilly, Fred Magumba, Patrick Okello, Eric D Mintz, Nina Marano, Jamae F Morris
Publikováno v: PLoS ONE, Vol 12, Iss 7, p e0180864 (2017)
Globally, an estimated 2.5 billion people lack access to improved sanitation. Unimproved sanitation increases the risk of morbidity and mortality, especially in protracted refugee situations where sanitation is based on pit latrine use. Once the pit
Externí odkaz: https://doaj.org/article/2cc4147be50a49b3ad23f8c4386e9895
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3
Akademický článek
Interleukin-6 receptor polymorphism is prevalent in HIV-negative Castleman Disease and is associated with increased soluble interleukin-6 receptor levels.
Autor: Katie Stone, Emily Woods, Susann M Szmania, Owen W Stephens, Tarun K Garg, Bart Barlogie, John D Shaughnessy, Brett Hall, Manjula Reddy, Antje Hoering, Emily Hansen, Frits van Rhee
Publikováno v: PLoS ONE, Vol 8, Iss 1, p e54610 (2013)
Multicentric Castleman Disease is largely driven by increased signaling in the pathway for the plasma cell growth factor interleukin-6. We hypothesized that interleukin-6/interleukin-6 receptor/gp130 polymorphisms contribute to increased interleukin-
Externí odkaz: https://doaj.org/article/e3ad366ca5e447239d64c13d6fd64cf0
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6
Report of two children with global developmental delay in association with de novo TLK2 variant and literature review
Autor: Meena Balasubramanian, Emily Woods, Michael Spiller
Publikováno v: American Journal of Medical Genetics Part A. 188:931-940
We describe clinical details, including novel findings, of two further children with the newly defined TLK2-related disorder. One patient was recruited to the Deciphering Developmental Delay (DDD) Study to identify underlying etiology of global devel
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::25ab45fb1ac076379220ea6f076764dc
https://doi.org/10.1002/ajmg.a.62580
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7
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype
Autor: Schaida Schirwani, Emily Woods, David A. Koolen, Charlotte W. Ockeloen, Sally Ann Lynch, Karl Kavanagh, John M. Graham, Katheryn Grand, Tyler Mark Pierson, Jeffrey M. Chung, Meena Balasubramanian
Publikováno v: American Journal of Medical Genetics. Part A, 191, 29-36
American Journal of Medical Genetics. Part A, 191, 1, pp. 29-36
Contains fulltext : 291387.pdf (Publisher’s version ) (Open Access) De novo truncating and splicing pathogenic variants in the Additional Sex Combs-Like 3 (ASXL3) gene are known to cause neurodevelopmental delay, intellectual disability, behavioral
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a08f8f797a7a71ef9e6ba6788406f1c
https://pubmed.ncbi.nlm.nih.gov/36177608
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