Search Results - "Bate, Louise"

Multidisciplinary approach to the treatment of an oblique crown–root fracture by Bate, Anna‐Louise, Lerda, Fabrizio

“…–  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…”
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How clinical decisions are made by Bate, Louise, Hutchinson, Andrew, Underhill, Jonathan, Maskrey, Neal

“…There is much variation in the implementation of the best available evidence into clinical practice. These gaps between evidence and practice are often a…”
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Molecular genetics of human epilepsies by Bate, Louise, Gardiner, Mark

“…The term epilepsy encompasses a heterogeneous group of disorders, with a lifetime cumulative incidence of 3%. Genetic factors are thought to contribute to the…”
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Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12 by SANDER, Thomas, WINDEMUTH, Christine, BULTEAU, Christine, KAMINSKA, Anna, CIEUTA, Cécile, PRUD'HOMME, Jean-Francois, DULAC, Olivier, BATE, Louise, ROBINSON, Robert, GARDINER, R. Mark, COVANIS, Athanasios, DE HAAN, Gerrit-Jan, SCHULZ, Herbert, JANSSEN, Guus A. M. A. J, VAN ERP, M. Gerard, BOEZEMAN, Eduard H. J. F, LINDHOUT, Dick, HEILS, Armin, NÜRNBERG, Peter, JANZ, Diéter, SAAR, Kathrin, GENNARO, Elena, RIGGIO, Concetta, BIANCHI, Amedeo, ZARA, Federico, RUDOLF, Gabrielle, PICARD, Fabienne

“…A recent genome-wide scan revealed a major susceptibility locus for idiopathic generalized epilepsies (IGEs) in the chromosomal region 8p12 in 32 IGE families…”
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How clinical decisions are made: Prescribing Themed Issue by BATE, Louise, HUTCHINSON, Andrew, UNDERHILL, Jonathan, MASKREY, Neal

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Genome search for susceptibility loci of common idiopathic generalised epilepsies by SANDER, T, SCHULZ, H, VILLE, D, CIEUTA, C, PICARD, F, PRUD'HOMME, J.-F, BATE, L, SUNDQUIST, A, GARDINER, R. M, JANSSEN, G. A. M. A. J, DE HAAN, G.-J, KASTELEIJN-NOLST-TRENITE, D. G. A, SAAR, K, BADER, A, LINDHOUT, D, RIESS, O, WIENKER, T. F, JANZ, D, REIS, A, GENNARO, E, RIGGIO, M. C, BIANCHI, A, ZARA, F, LUNA, D, BULTEAU, C, KAMINSKA, A

“…Genetic factors play a major role in the aetiology of idiopathic generalised epilepsies (IGEs). The present genome scan was designed to identify susceptibility…”
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Genetics of inherited epilepsies by Bate, Louise, Gardiner, Mark

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Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus ( EJM2) on chromosome 15q13–14 by Taske, Nichole L., Williamson, Magali P., Makoff, Andrew, Bate, Louise, Curtis, David, Kerr, Michael, Kjeldsen, Marianne J., Pang, Kiang An, Sundqvist, Anders, Friis, Mogens L., Chadwick, David, Richens, Alan, Covanis, Athanasios, Santos, Manuela, Arzimanoglou, Alexis, Panayiotopoulos, Chrysostomos P., Whitehouse, William P., Rees, Michele, Gardiner, R.Mark

“…A previous study of 34 nuclear pedigrees segregating juvenile myoclonic epilepsy (JME) gave significant evidence of linkage with heterogeneity to marker loci…”
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No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1 by Sander, Thomas, Windemuth, Christine, Schulz, Herbert, Saar, Kathrin, Gennaro, Elena, Bianchi, Amedeo, Zara, Federico, Bulteau, Christine, Kaminska, Anna, Ville, Dorothée, Cieuta, Cécile, Prud'homme, Jean-François, Dulac, Olivier, Bate, Louise, Gardiner, R. Mark, de Haan, Gerrit-Jan, Janssen, Guus A.M.A.J., Witte, Jorine, Halley, Dicky J.J., Lindhout, Dick, Wienker, Thomas F., Janz, Dieter

“…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…”
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Evaluation of the positional candidate gene CHRNA 7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14 by TASKE, Nichole L, WILLIAMSON, Magali P, CHADWICK, David, RICHENS, Alan, COVANIS, Athanasios, SANTOS, Manuela, ARZIMANOGLOU, Alexis, PANAYIOTOPOULOS, Chrysostomos P, WHITEHOUSE, William P, REES, Michele, GARDINER, R. Mark, MAKOFF, Andrew, BATE, Louise, CURTIS, David, KERR, Michael, KJELDSEN, Marianne J, KIANG AN PANG, SUNDQVIST, Anders, FRIIS, Mogens L

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Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8 by Mitchell, Wayne A., Wheeler, Ruth B., Sharp, Julie D., Bate, S. Louise, Gardiner, R. Mark, Ranta, U. Susanna, Lonka, Liina, Williams, Ruth E., Lehesjoki, Anna-Elina, Mole, Sara E.

“…One variant form of late infantile neuronal ceroid lipofuscinosis (LINCL) is found predominantly within the Turkishpopulation ( CLN7). Exclusion mapping showed…”
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Multidisciplinary approach to the treatment of an oblique crown-root fracture by Bate, Anna-Louise, Lerda, Fabrizio

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