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Refinado por: assunto: Medical Sciences remover assunto: Nervous System remover
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Human herpesvirus 6 and 7 in febrile status epilepticus: The FEBSTAT study
Human herpesvirus 6 and 7 in febrile status epilepticus: The FEBSTAT study
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Human herpesvirus 6 and 7 in febrile status epilepticus: The FEBSTAT study

Epstein, Leon G. ; Shinnar, Shlomo ; Hesdorffer, Dale C. ; Nordli, Douglas R. ; Hamidullah, Aaliyah ; Benn, Emma K. T. ; Pellock, John M. ; Frank, L. Matthew ; Lewis, Darrell V. ; Moshe, Solomon L. ; Shinnar, Ruth C. ; Sun, Shumei

Epilepsia (Copenhagen), 2012-09, Vol.53 (9), p.1481-1488 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Narcolepsy, 2009 A(H1N1) pandemic influenza, and pandemic influenza vaccinations: What is known and unknown about the neurological disorder, the role for autoimmunity, and vaccine adjuvants
Narcolepsy, 2009 A(H1N1) pandemic influenza, and pandemic influenza vaccinations: What is known and unknown about the neurological disorder, the role for autoimmunity, and vaccine adjuvants
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Narcolepsy, 2009 A(H1N1) pandemic influenza, and pandemic influenza vaccinations: What is known and unknown about the neurological disorder, the role for autoimmunity, and vaccine adjuvants

Ahmed, S. Sohail ; Schur, Peter H ; MacDonald, Noni E ; Steinman, Lawrence

Journal of autoimmunity, 2014-05, Vol.50, p.1-11 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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3
Narcolepsy and influenza A(H1N1) pandemic 2009 vaccination in the United States
Narcolepsy and influenza A(H1N1) pandemic 2009 vaccination in the United States
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Narcolepsy and influenza A(H1N1) pandemic 2009 vaccination in the United States

Duffy, Jonathan ; Weintraub, Eric ; Vellozzi, Claudia ; DeStefano, Frank

Neurology, 2014-11, Vol.83 (20), p.1823-1830 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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4
Genome-wide association study identifies 19p13.3 ( UNC13A ) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Genome-wide association study identifies 19p13.3 ( UNC13A ) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
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Genome-wide association study identifies 19p13.3 ( UNC13A ) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Giegling, Ina ; Lemmens, Robin ; Kiemeney, Lambertus A ; Ophoff, Roel A ; Zwarts, Machiel J ; Hofman, Albert ; Hendrich, Corinna ; Landers, John E ; Saris, Christiaan G J ; Veldink, Jan H ; Melki, Judith ; Fumoto, Katsumi ; Andersen, Peter M ; Birve, Anna ; Schreiber, Stefan ; de Visser, Marianne ; Hardiman, Orla ; Uitterlinden, Andre G ; Nöthen, Markus M ; Meininger, Vincent ; Waibel, Stefan ; Cichon, Sven ; Leigh, P Nigel ; Wichmann, H-Erich ; Ludolph, Albert C ; van Es, Michael A ; Vermeulen, Sita H H M ; Robberecht, Wim ; Meyer, Thomas ; Schelhaas, Helenius J ; van Vught, Paul W J ; Groen, Ewout J N ; Rivadeneira, Fernando ; Purcell, Shaun ; Cronin, Simon ; Estrada, Karol ; van den Berg, Leonard H ; Glass, Jonathan D ; Huisman, Mark H B ; Slowik, Agnieszka ; Wokke, John H J ; Pasterkamp, R Jeroen ; Brown, Robert H ; Shaw, Christopher E ; van der Kooi, Anneke J ; Tomik, Barbara ; van Doormaal, Perry T C ; Rujescu, Dan ; McLaughlin, Russell L ; Dahlberg, Caroline ; Al-Chalabi, Ammar ; Blauw, Hylke M ; Strengman, Eric ; Muglia, Pierandrea

Nature genetics, 2009-10, Vol.41 (10), p.1083-1087 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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5
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
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Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Burnside, Rachel D. ; Pasion, Romela ; Mikhail, Fady M. ; Carroll, Andrew J. ; Robin, Nathaniel H. ; Youngs, Erin L. ; Gadi, Inder K. ; Keitges, Elizabeth ; Jaswaney, Vikram L. ; Papenhausen, Peter R. ; Potluri, Venkateswara R. ; Risheg, Hiba ; Rush, Brooke ; Smith, Janice L. ; Schwartz, Stuart ; Tepperberg, James H. ; Butler, Merlin G.

Human genetics, 2011-10, Vol.130 (4), p.517-528 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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6
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
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Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Illig, Thomas ; Holsboer, Florian ; Stiasny-Kolster, Karin ; Xiong, Lan ; Trenkwalder, Claudia ; Eckstein, Gertrud ; Montplaisir, Jacques ; Wichmann, H-Erich ; Schormair, Barbara ; Gieger, Christian ; Meitinger, Thomas ; Oertel, Wolfgang ; Lichtner, Peter ; Pütz, Benno ; Paulus, Walter ; Turecki, Gustavo ; Jalilzadeh, Shapour ; Bachmann, Cornelius G ; Peglau, Ines ; Winkelmann, Juliane ; Müller-Myhsok, Bertram ; Fulda, Stephany ; Ripke, Stephan ; Zimprich, Alexander ; Hauk, Stephanie ; Rouleau, Guy ; Eisensehr, Ilonka

Nature genetics, 2007-08, Vol.39 (8), p.1000-1006 [Periódico revisado por pares]

London: Nature Publishing Group

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7
BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas
BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas
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BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas

Idbaih, Ahmed ; Marie, Yannick ; Lucchesi, Carlo ; Pierron, Gaëlle ; Manié, Elodie ; Raynal, Virginie ; Mosseri, Véronique ; Hoang‐Xuan, Khê ; Kujas, Michèle ; Brito, Isabel ; Mokhtari, Karima ; Sanson, Marc ; Barillot, Emmanuel ; Aurias, Alain ; Delattre, Jean‐Yves ; Delattre, Olivier

International journal of cancer, 2008-04, Vol.122 (8), p.1778-1786 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Motor Coordination in Autism Spectrum Disorders: A Synthesis and Meta-Analysis
Motor Coordination in Autism Spectrum Disorders: A Synthesis and Meta-Analysis
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Motor Coordination in Autism Spectrum Disorders: A Synthesis and Meta-Analysis

Fournier, Kimberly A. ; Hass, Chris J. ; Naik, Sagar K. ; Lodha, Neha ; Cauraugh, James H.

Journal of autism and developmental disorders, 2010-10, Vol.40 (10), p.1227-1240 [Periódico revisado por pares]

Boston: Springer US

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9
Evidence of Disturbed Sleep and Increased Illness in Overreached Endurance Athletes
Evidence of Disturbed Sleep and Increased Illness in Overreached Endurance Athletes
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Evidence of Disturbed Sleep and Increased Illness in Overreached Endurance Athletes

HAUSSWIRTH, CHRISTOPHE ; LOUIS, JULIEN ; AUBRY, ANAËL ; BONNET, GUILLAUME ; DUFFIELD, ROB ; LE MEUR, YANN

Medicine and science in sports and exercise, 2014-05, Vol.46 (5), p.1036-1045 [Periódico revisado por pares]

Hagerstown, MD: American College of Sports Medicine

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10
Long-term Valacyclovir Suppressive Treatment After Herpes Simplex Virus Type 2 Meningitis: A Double-Blind, Randomized Controlled Trial
Long-term Valacyclovir Suppressive Treatment After Herpes Simplex Virus Type 2 Meningitis: A Double-Blind, Randomized Controlled Trial
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Long-term Valacyclovir Suppressive Treatment After Herpes Simplex Virus Type 2 Meningitis: A Double-Blind, Randomized Controlled Trial

Aurelius, E. ; Franzen-Röhl, E. ; Glimåker, M. ; Akre, O. ; Grillner, L. ; Jorup-Rönström, C. ; Studahl, M.

Clinical infectious diseases, 2012-05, Vol.54 (9), p.1304-1313 [Periódico revisado por pares]

Oxford: Oxford University Press

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