Search Results - "Yates, T.M."

Calcium requests in a primary care; An observational audit of biochemical requests and frequency of abnormal results by Sillars, A., Livingstone, R., Yates, T.M., Godber, I.M., Gallacher, S.J., Gibb, F.W., Leese, G.P., Kennon, B.

“…This aim of this audit was to assess the extent of serum calcium testing and the frequency of hypercalcaemia in the primary care setting. We also assessed the…”
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Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype by Balasubramanian, Meena, Dingemans, Alexander J M, Albaba, Shadi, Richardson, Ruth, Yates, Thabo M, Cox, Helen, Douzgou, Sofia, Armstrong, Ruth, Sansbury, Francis H, Burke, Katherine B, Fry, Andrew E, Ragge, Nicola, Sharif, Saba, Foster, Alison, De Sandre-Giovannoli, Annachiara, Elouej, Sahar, Vasudevan, Pradeep, Mansour, Sahar, Wilson, Kate, Stewart, Helen, Heide, Solveig, Nava, Caroline, Keren, Boris, Demirdas, Serwet, Brooks, Alice S, Vincent, Marie, Isidor, Bertrand, Küry, Sebastien, Schouten, Meyke, Leenders, Erika, Chung, Wendy K, Haeringen, Arie van, Scheffner, Thomas, Debray, Francois-Guillaume, White, Susan M, Palafoll, Maria Irene Valenzuela, Pfundt, Rolph, Newbury-Ecob, Ruth, Kleefstra, Tjitske

“…Witteveen-Kolk syndrome (OMIM 613406) is a recently defined neurodevelopmental syndrome caused by heterozygous loss-of-function variants in SIN3A. We define…”
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Baraitser–Winter cerebrofrontofacial syndrome by Yates, T.M., Turner, C.L., Firth, H.V., Berg, J., Pilz, D.T.

“…Baraitser–Winter cerebrofrontofacial syndrome (BWCFF) (BRWS; MIM #243310, 614583) is a rare developmental disorder affecting multiple organ systems. It is…”
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Creation and evaluation of full-text literature-derived, feature-weighted disease models of genetically determined developmental disorders by Yates, T M, Lain, A, Campbell, J, FitzPatrick, D R, Simpson, T I

“…There are >2500 different genetically determined developmental disorders (DD), which, as a group, show very high levels of both locus and allelic…”
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Prior D1 dopamine receptor stimulation is required to primeD2-mediated striatal Fos expression in 6-hydroxydopamine-lesioned rats by Pollack, A.E., Yates, T.M.

“…Repeated dopamine agonist administration to rats with unilateral 6-hydroxydopamine lesions of the nigrostriatal pathway potentiates behavioral and neuronal…”
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Distortion of pyelogram by extrarenal lesion; liver abscess distortion of pyelogram by YATES, T M

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Vestigial epididymal structures in unilateral renal aplasia by CICCHINO, F E, VATES, T M, CHAPPELL, B S

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