Movement Disorders (revue) - Exploration (Accueil)

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Chickens < Child < Child Development  Facettes :

List of bibliographic references indexed by Child

Number of relevant bibliographic references: 401.
[0-20] [0 - 20][0 - 50][20-40]
Ident.Authors (with country if any)Title
000117 (2015) Jeremiah M. Scharf [États-Unis] ; Laura L. Miller ; Caitlin A. Gauvin ; Janelle Alabiso ; Carol A. Mathews ; Yoav Ben-ShlomoPopulation prevalence of Tourette syndrome: a systematic review and meta-analysis.
000299 (2015) Eman M. Khedr [Égypte] ; Mohamed A. Ahmed ; Anwar M. Ali ; Reda Badry ; John C. RothwellChanges in motor cortical excitability in patients with Sydenham's chorea.
000365 (2014) Shiguo Liu [République populaire de Chine] ; Jiajia Cui ; Xinhua Zhang ; Weifeng Wu ; Haitao Niu ; Xu Ma ; Hongmei Xu ; Mingji YiVariable number tandem repeats in dopamine receptor D4 in Tourette's syndrome.
000415 (2014) Signe S Ndergaard Jeppesen [Danemark] ; Nanette Mol Debes ; Helle Juhl Simonsen ; Egill Rostrup ; H B W. Larsson ; Liselotte SkovStudy of medication-free children with Tourette syndrome do not show imaging abnormalities.
000418 (2014) Michał Sobstyl [Pologne] ; Mirosław Z Bek ; Tomasz Kmie ; Jarosław Sławek ; Karol P. BudohoskiStatus dystonicus due to internal pulse generator depletion in a patient with primary generalized dystonia.
000421 (2014) Claudia Dufke [Allemagne] ; Marc Sturm ; Christopher Schroeder ; Susanne Moll ; Thomas Ott ; Olaf Riess ; Peter Bauer ; Kathrin GrundmannScreening of mutations in GNAL in sporadic dystonia patients.
000444 (2014) Jean-Marc Trocello [France] ; Souleiman El Balkhi ; France Woimant ; Nadège Girardot-Tinant ; Philippe Chappuis ; Carla Lloyd ; Joël PouponRelative exchangeable copper: a promising tool for family screening in Wilson disease.
000454 (2014) Martje E. Van Egmond [Pays-Bas] ; Corien C. Verschuuren-Bemelmans ; Esther A. Nibbeling ; Jan Willem J. Elting ; Deborah A. Sival ; Oebele F. Brouwer ; Jeroen J. De Vries ; Hubertus P. Kremer ; Richard J. Sinke ; Marina A. Tijssen ; Tom J. De KoningRamsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation.
000462 (2014) Ali S. Shalash [Égypte] ; Solaf M. Elsayed ; Suzan Elnaghi ; Susanne A. Schneider ; Tawhida Y. Abdel GhaffarProminent extensor truncal dystonia in Egyptian patients with Wilson's disease.
000506 (2014) Michelangelo Mancuso [Italie] ; Daniele Orsucci ; Corrado Angelini ; Enrico Bertini ; Michela Catteruccia ; Elena Pegoraro ; Valerio Carelli ; Maria L. Valentino ; Giacomo P. Comi ; Carlo Minetti ; Claudio Bruno ; Maurizio Moggio ; Elena Caldarazzo Ienco ; Tiziana Mongini ; Liliana Vercelli ; Guido Primiano ; Serenella Servidei ; Paola Tonin ; Mauro Scarpelli ; Antonio Toscano ; Olimpia Musumeci ; Isabella Moroni ; Graziella Uziel ; Filippo M. Santorelli ; Claudia Nesti ; Massimiliano Filosto ; Costanza Lamperti ; Massimo Zeviani ; Gabriele SicilianoMyoclonus in mitochondrial disorders.
000512 (2014) Shekeeb S. Mohammad [Australie] ; Victor S C. Fung ; Padraic Grattan-Smith ; Deepak Gill ; Sekhar Pillai ; Sudarshini Ramanathan ; Fabienne Brilot ; Russell C. DaleMovement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies.
000531 (2014) Subhashie Wijemanne [États-Unis] ; Laura J C. Wu ; Joseph Jankovic [États-Unis]Long-term efficacy and safety of fluphenazine in patients with Tourette syndrome.
000543 (2014) Masayuki Sasaki [Japon] ; Atsushi Ishii ; Yoshiaki Saito ; Shinichi HiroseIntermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.
000553 (2014) Amanda J. Thompson ; Sankarasubramoney H. Subramony ; Michael S. OkunI spy apraxic eyes in spinocerebellar ataxia type 2: a false-negative ataxia panel.
000560 (2014) Rachel Saunders-Pullman [États-Unis] ; Tania Fuchs [États-Unis] ; Marta San Luciano [États-Unis] ; Deborah Raymond [États-Unis] ; Alison Brashear [États-Unis] ; Robert Ortega [États-Unis] ; Andres Deik [États-Unis] ; Laurie J. Ozelius [États-Unis] ; Susan B. Bressman [États-Unis]Heterogeneity in primary dystonia: lessons from THAP1, GNAL and TOR1A in Amish-Mennonites
000561 (2014) Shekeeb S. Mohammad [Australie] ; Kate Sinclair ; Sekhar Pillai ; Vera Merheb ; Tim D. Aumann ; Deepak Gill ; Russell C. Dale ; Fabienne BrilotHerpes simplex encephalitis relapse with chorea is associated with autoantibodies to N-Methyl-D-aspartate receptor or dopamine-2 receptor.
000563 (2014) Martin B. Delatycki [Australie] ; Geneieve Tai ; Louise Corben ; Eppie M. Yiu ; Marguerite V. Evans-Galea ; Sarah E M. Stephenson ; Lyle Gurrin ; Katrina J. Allen ; David Lynch ; Paul J. LockhartHFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia.
000590 (2014) Margaret O'Brien [Irlande (pays)] ; Mary Reilly ; Brian Sweeney ; Cathal Walsh ; Michael HutchinsonEpidemiology of Wilson's disease in Ireland.
000609 (2014) Valerija Dobri I [Allemagne] ; Nikola Kresojevi ; Ana Westenberger ; Marina Svetel ; Aleksandra Tomi ; Vesna Rali ; Igor Petrovi ; Milica Je Menica Luki ; Katja Lohmann ; Ivana Novakovi ; Christine Klein ; Vladimir S. KostiDe novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
000610 (2014) Ryosuke Miyamoto [Japon] ; Hidetaka Koizumi ; Hiroyuki Morino ; Toshitaka Kawarai ; Hirofumi Maruyama ; Yohei Mukai ; Ai Miyashiro ; Wataru Sako ; Yuishin Izumi ; Hideshi Kawakami ; Ryuji KajiDYT6 in Japan-genetic screening and clinical characteristics of the patients.
000611 (2014) Michael Zech [Allemagne] ; Florian Castrop ; Barbara Schormair ; Angela Jochim ; Thomas Wieland ; Nadine Gross ; Peter Lichtner ; Annette Peters ; Christian Gieger ; Thomas Meitinger ; Tim M. Strom ; Konrad Oexle ; Bernhard Haslinger ; Juliane WinkelmannDYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia family.

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