Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Louise Bate"'
Publikováno v:
British Journal of Clinical Pharmacology. 74:614-620
There is much variation in the implementation of the best available evidence into clinical practice. These gaps between evidence and practice are often a result of multiple individual decisions. When making a decision, there is so much potentially re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0db9f23d36c147ffcd7ec94fde1f77aa
https://doi.org/10.1111/j.1365-2125.2012.04366.x
https://doi.org/10.1111/j.1365-2125.2012.04366.x
Autor:
David Jones, Jonathan Gower, Daniel Morris, Fiona Brennan, John Hitchman, S Michael Kinsella, Clifford Shelton, Victoria Pegna, Rebecca Knagg, Max Clayton-Smith, Hrishi Narayanan, Louise Bates, Mike Donnellon, Jenny Dorey, Bob Evans, Yasmina Hamdaoui, Cathy Lawson, Tracey Radcliffe, Olivia Schaff, Tim Sheppard, Jennifer Strong, Beck Diedo
Publikováno v:
BMJ Open, Vol 13, Iss 3 (2023)
Objectives To agree on the ‘top 10’ research priorities for environmentally sustainable perioperative practice.Design Surveys and literature review; final consensus workshop using a nominal group technique.Setting UK-based setting.Participants He
Externí odkaz:
https://doaj.org/article/fe9cf404f0cf4b81a738b7bf829bdc8b
Autor:
Mark Gardiner, Louise Bate
Publikováno v:
Expert Reviews in Molecular Medicine. 1:1-22
The term epilepsy encompasses a heterogeneous group of disorders, with a lifetime cumulative incidence of 3%. Genetic factors are thought to contribute to the aetiology in up to 60% of cases. Various molecular and cellular mechanisms give rise to epi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ba979cab130a7a7be2f02b373e4cd8b
https://doi.org/10.1017/s1462399499001349
https://doi.org/10.1017/s1462399499001349
Autor:
Anna-Louise Bate, Fabrizio Lerda
Publikováno v:
Dental traumatology : official publication of International Association for Dental Traumatology. 26(1)
This case report describes the management of an oblique crown-root fracture of the buccal cusp of the upper right first premolar. After removal of the fractured cusp, a provisional restorative build-up in this area was carried out, in order to carry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715b9d92a059a38b3543ae7fc94e21de
https://pubmed.ncbi.nlm.nih.gov/20089068
https://pubmed.ncbi.nlm.nih.gov/20089068
Autor:
Louise Bate, Christine Windemuth, Dicky J. J. Halley, Guus A M A J Janssen, R. Mark Gardiner, Dick Lindhout, Jorine Witte, Jean François Prud'homme, Gerrit-Jan de Haan, Anna Kaminska, Thomas Sander, C. Cieuta, Elena Gennaro, Federico Zara, Kathrin Saar, Olivier Dulac, Christine Bulteau, Dorothée Ville, Dieter Janz, Thomas F. Wienker, Amedeo Bianchi, Herbert Schulz
Publikováno v:
American journal of medical genetics. 114(6)
A recent genome-wide scan showed strong evidence for a major locus for common syndromes of idiopathic generalized epilepsy (IGE) at the marker D18S474 on chromosome 18q21.1 (LOD score 4.5/5.2 multipoint/two-point). The present replication study teste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732796d31365c309190b93581b8f19ad
https://pubmed.ncbi.nlm.nih.gov/12210286
https://pubmed.ncbi.nlm.nih.gov/12210286
Autor:
Christine Windemuth, Jean François Prud'homme, R Nabbout-Tarantino, RM Gardiner, Louise Bate, Olivier Dulac, D. Janz, Anna Kaminska, Herbert Schulz, Dick Lindhout, Thomas Sander, Federico Zara, Kathrin Saar, Elena Gennaro, Christine Bulteau, Dorothée Ville, Amedeo Bianchi, Thomas F. Wienker, C. Cieuta
Publikováno v:
Windemuth, C, Schultz, H, Saar, K, Cennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Nabbout-Tarantino, R, Prud'homme, J F, Dulac, O, Bate, L, Gardiner, R M, Lindhout, D, Wienker, T F, Janz, D & Sander, T 2002, ' No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures ', Epilepsy Research, vol. 51, pp. 23-29 .
A recent genome-wide scan revealed suggestive evidence for two susceptibility loci for idiopathic generalized epilepsy (IGE) in the chromosomal regions 5p15 and 5q14-q22 in families with typical absence seizures. The present replication study tested
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7643bdb1808fe2e792655f7baf28773
https://portal.findresearcher.sdu.dk/da/publications/8d2e8070-6fcf-11db-81a9-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/8d2e8070-6fcf-11db-81a9-000ea68e967b
Autor:
Thomas F. Wienker, M. Concetta Riggio, R. Mark Gardiner, Anders Sundquist, Dick Lindhout, Guus A M A J Janssen, Louise Bate, Fabienne Picard, Jean François Prud'homme, Herbert Schulz, Olaf Riess, Dorothée G A Kasteleijn-Nolst-Trenité, Kathrin Saar, Amedeo Bianchi, C. Cieuta, David Luna, Federico Zara, Dieter Janz, Anna Kaminska, Christine Bulteau, Dorothée Ville, André Reis, Adri J. Bader, Elena Gennaro, Gerrit-Jan de Haan, Thomas Sander
Publikováno v:
Human molecular genetics, Vol. 9, No 10 (2000) pp. 1465-1472
Human Molecular Genetics, 9(10), 1465-1472. Oxford University Press
Scopus-Elsevier
Human Molecular Genetics, 9(10), 1465-1472. Oxford University Press
Scopus-Elsevier
Genetic factors play a major role in the aetiology of idiopathic generalised epilepsies (IGEs). The present genome scan was designed to identify susceptibility loci that predispose to a spectrum of common IGE syndromes. Our collaborative study includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05dd4c5906bedfa75204da7ec6bc3e3f
https://hdl.handle.net/11567/1026675
https://hdl.handle.net/11567/1026675
Autor:
Louise Bate, Mark Gardiner
Publisher Summary This chapter discusses the genetics of idiopathic epilepsy. Epilepsy is a disorder of the brain characterized by recurrent, unprovoked epileptic seizures. Epilepsy may occur as a feature of a disease, in which there is a common etio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::889b5f5c555b3700867bda6f4b66c10e
https://doi.org/10.1016/s0921-0709(99)80062-5
https://doi.org/10.1016/s0921-0709(99)80062-5