Movement Disorders (etiology) < Movement Disorders (genetics) < Movement Disorders (history)

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List of bibliographic references indexed by Movement Disorders (genetics)

Number of relevant bibliographic references: 50.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000511 (2014)	Marcie L. Rabin [États-Unis] ; Claire Stevens-Haas ; Emilyrose Havrilla ; Tanvi Devi ; Roger Kurlan	Movement disorders in women: a review.
000572 (2014)	Pietro Cortelli [Italie] ; Margherita Fabbri ; Giovanna Calandra-Buonaura ; Sabina Capellari ; Paolo Tinuper ; Piero Parchi ; Elio Lugaresi	Gait disorders in fatal familial insomnia.
000576 (2014)	Daniel F. Tardiff [États-Unis] ; Vikram Khurana ; Chee Yeun Chung ; Susan Lindquist	From yeast to patient neurons and back again: powerful new discovery platform.
000635 (2014)	Jared F. Cook [États-Unis] ; Deborah F. Hill [États-Unis] ; Beverly M. Snively [États-Unis] ; Niki Boggs [États-Unis] ; Cynthia K. Suerken [États-Unis] ; Ihtsham Haq [États-Unis] ; Mark Stacy [États-Unis] ; W. Vaughn Mccall [États-Unis] ; Laurie J. Ozelius [États-Unis] ; Kathleen J. Sweadner [États-Unis] ; Allison Brashear [États-Unis]	Cognitive Impairment in Rapid-Onset Dystonia-Parkinsonism
000903 (2013)	Wilhelmina G. Leen [Pays-Bas] ; Leena Mewasingh ; Marcel M. Verbeek ; Erik-Jan Kamsteeg ; Bart P. Van De Warrenburg ; Michel A. Willemsen	Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
000915 (2013)	Susan H. Fox [Canada]	Metabolic disorders causing movement disorders in childhood; an addition to the list.
000A37 (2013)	Eugenia Storti ; Francesca Cortese ; Roberto Di Fabio ; Chiara Fiorillo ; Alberto Pierallini ; Alessandra Tessa ; Annamaria Valleriani ; Francesco Pierelli ; Filippo M. Santorelli ; Carlo Casali	De novo FTL mutation: a clinical, neuroimaging, and molecular study.
000B04 (2013)	Raja Mehanna [États-Unis] ; Christine Hunter ; Anthony Davidson ; Joohi Jimenez-Shahed ; Joseph Jankovic [États-Unis]	Analysis of CYP2D6 genotype and response to tetrabenazine.
000B37 (2013)	Kaori Itokawa [Japon] ; Takeshi Sekine ; Manabu Funayama ; Hiroyuki Tomiyama ; Miki Fukui ; Toshimasa Yamamoto ; Naotoshi Tamura ; Hiroshi Matsuda ; Nobutaka Hattori ; Nobuo Araki	A case of α-synuclein gene duplication presenting with head-shaking movements.
000B38 (2013)	Fiore Manganelli ; Raffaele Dubbioso ; Marcello Esposito ; Caterina Marin ; Chiara Pisciotta ; Salvatore Pignatelli ; Lucio Santoro	A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder.
000B93 (2012)	James T. Teo [Royaume-Uni] ; Mark J. Edwards ; Kailash Bhatia	Tardive dyskinesia is caused by maladaptive synaptic plasticity: a hypothesis.
001554 (2011)	C. Warren Olanow [États-Unis] ; Kathryn B. Wunderle [États-Unis] ; Karl Kieburtz [États-Unis]	Milestones in movement disorders clinical trials: Advances and landmark studies
001640 (2011)	Marie Chauveau [France] ; Nathalie Damon-Perriere [France] ; Chrystelle Latxague [France] ; Umberto Spampinato [France] ; Hans Jung [Suisse] ; Pierre Burbaud [France] ; François Tison [France]	Head drops are also observed in McLeod syndrome
001714 (2011)	Aida Ormazabal [Espagne] ; Mercedes Serrano [Espagne] ; Angels Garcia-Cazorla [Espagne] ; Jaume Campistol [Espagne] ; Rafael Artuch [Espagne] ; Pedro Castro De Castro [Espagne] ; Estíbaliz Barredo-Valderrama [Espagne] ; Judith Armstrong [Espagne] ; Claudio Toma [Espagne] ; Bru Cormand [Espagne]	Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype
001947 (2010)	Roser Pons [Grèce] ; Abbie Collins [États-Unis] ; Michael Rotstein [États-Unis] ; Kristin Engelstad [États-Unis] ; Darryl C. De Vivo [États-Unis]	The spectrum of movement disorders in Glut‐1 deficiency
001C15 (2010)	Hans C. Scholle [Allemagne] ; H. A. Jinnah [États-Unis] ; Dirk Arnold [Allemagne] ; Frank H. W. Biedermann [Allemagne] ; Bernd Faenger [Allemagne] ; Roland Grassme [Allemagne] ; Ellen J. Hess [États-Unis] ; Nikolaus P. Schumann [Allemagne]	Kinematic and electromyographic tools for characterizing movement disorders in mice
002194 (2009)	Kiyoka Kinugawa [France] ; Marie Vidailhet [France] ; Fabienne Clot [France] ; Emmanuelle Apartis [France] ; David Grabli [France] ; Emmanuel Roze [France]	Myoclonus‐dystonia: An update
002201 (2009)	Jan Edler [Allemagne] ; Brit Mollenhauer [États-Unis] ; Uta Heinemann [Allemagne] ; Daniela Varges [Allemagne] ; Carola Werner [Allemagne] ; Inga Zerr [Allemagne] ; Walter J. Schulz-Schaeffer [Allemagne]	Movement disturbances in the differential diagnosis of Creutzfeldt‐Jakob disease
002296 (2009)	Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Ines Garcia-Gorostiaga [Royaume-Uni, Espagne] ; Niall P. Quinn [Royaume-Uni] ; Yvonne G. Weber ; Holger Lerche [Allemagne] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias
002397 (2009)	Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]	Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)
002476 (2009)	Akatsuki Kubota [Japon] ; Ayumi Hida [Japon] ; Yaeko Ichikawa [Japon] ; Yoshio Momose [Japon] ; Jun Goto [Japon] ; Yukifusa Igeta [Japon] ; Hideji Hashida [Japon] ; Kunihiro Yoshida [Japon] ; Syu-Ichi Ikeda [Japon] ; Ichiro Kanazawa [Japon] ; Shoji Tsuji [Japon]	A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations

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