Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Simon Pimstone"'
Autor:
Isabella Premoli, Pierre G. Rossini, Paul Y. Goldberg, Kristina Posadas, Louise Green, Noah Yogo, Simon Pimstone, Eugenio Abela, Gregory N. Beatch, Mark P. Richardson
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 11, Pp 2164-2174 (2019)
Abstract Objective Transcranial magnetic stimulation (TMS) produces characteristic deflections in the EEG signal named TMS‐evoked EEG potentials (TEPs), which can be used to assess drug effects on cortical excitability. TMS can also be used to dete
Externí odkaz:
https://doaj.org/article/1392a1ff0aba42a1b9d62614b06be7e9
Autor:
Raymond Y. Cho, BSc, Jian Weng, BSc, Kelsey Lynch, MSc, CGC, Phoebe Ng, BSc, Chad Brown, BSc, Alison M. Hoens, MSc, BScPT, Kevin Barry, Liam R. Brunham, MD, PhD, FRCPC, Simon Pimstone, MD, PhD, FRCPC
Publikováno v:
CJC Open, Vol 1, Iss 3, Pp 107-114 (2019)
Background: Optimal design of clinical programs for patients with premature atherosclerotic cardiovascular disease (ASCVD) (men aged ≤ 50 years, women aged ≤ 55 years) requires an understanding of their priorities. We aimed to explore patient and
Externí odkaz:
https://doaj.org/article/c5f4dd2edf17455db0ca38bea49d0bf8
Publikováno v:
Atherosclerosis. 340:35-43
Familial combined hyperlipidemia (FCHL) is one of the most common inherited lipid phenotypes, characterized by elevated plasma concentrations of apolipoprotein B-100 and triglycerides. The genetic inheritance of FCHL remains poorly understood. The go
Autor:
Alison Cutts, Sultan Chowdhury, Laszlo G Ratkay, Maryanne Eyers, Clint Young, Rostam Namdari, Jay A Cadieux, Navjot Chahal, Michael Grimwood, Zaihui Zhang, Sophia Lin, Ian Tietjen, Zhiwei Xie, Lee Robinette, Luis Sojo, Matthew Waldbrook, Michael Hayden, Tarek Mansour, Simon Pimstone, Y. Paul Goldberg, Michael Webb, Charles J. Cohen
Divalent metal transporter 1 (DMT1) cotransports ferrous iron and protons and is the primary mechanism for uptake of non-heme iron by enterocytes. Inhibitors are potentially useful as therapeutic agents to treat iron overload disorders such as heredi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84a8fd089f5e95fb80b88ed63e8dd321
https://doi.org/10.1101/2022.09.01.506269
https://doi.org/10.1101/2022.09.01.506269
Autor:
M. S.
Publikováno v:
BC Business. Oct2009, Vol. 37 Issue 10, p90-90. 1/8p. 1 Black and White Photograph.
Autor:
Claudine, Laurent, Dana, Niehaus, Stéphanie, Bauché, Douglas F, Levinson, Stéphane, Soubigou, Simon, Pimstone, Michael, Hayden, Irena, Mbanga, Robin, Emsley, Jean-François, Deleuze, Jacques, Mallet
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)
The purpose of this study was to determine whether genetic linkage or association could be observed between schizophrenia (SZ) and the CAG repeat polymorphisms within the genes KCNN3 (known previously as hSKCa3) and PPP2R2B (linked to Spino-Cerebella
Autor:
LAPOINTE, KIRK1
Publikováno v:
Business in Vancouver. 4/17/2023, Issue 1746, p2-2. 1/2p.
Autor:
Christelle Foucher, Stephanie Rattier, David M Flavell, Philippa J Talmud, Steve E Humphries, John J Kastelein, Amir Ayyobi, Simon Pimstone, Jiri Frohlich, Jean-Claude Ansquer, George Steiner
Publikováno v:
Pharmacogenetics; Dec2004, Vol. 14 Issue 12, p823-829, 7p
Publikováno v:
Business in Vancouver. 4/29/2024, Issue 1800, p14-20. 4p.
Publikováno v:
Fair Disclosure Wire (Quarterly Earnings Reports). 05/09/2017.