Movement Disorders (revue) - Checkpoint (Ncbi)

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List of bibliographic references

Number of relevant bibliographic references: 49.
[0-20] [0 - 20][0 - 49][20-40]
Ident.Authors (with country if any)Title
000317 (2000) F J Revilla [États-Unis] ; B A Racette ; J S PerlmutterChorea and jaw-opening dystonia as a manifestation of NeuroBehcet's syndrome.
000409 (2000) N. Gálvez-Jiménez [États-Unis] ; M R Hanson ; J. CabralDopa-resistant parkinsonism, oculomotor disturbances, chorea, mirror movements, dyspraxia, and dementia: the expanding clinical spectrum of hypoparathyroidism. A case report.
000468 (2001) B V Manyam [États-Unis] ; A S Walters ; K R NarlaBilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry.
000492 (2001) C. Yalçinkaya [Turquie] ; H. Apaydin ; S. Ozekmekçi ; K M GibsonDelayed-onset dystonia associated with 3-oxothiolase deficiency.
000704 (2002) Thomas Brandt [Allemagne] ; Stefan Glasauer ; Marianne DieterichVestibular brainstem disorders: clinical syndromes in roll plane and their model simulation.
000815 (2002) F. Supiot [Belgique] ; M D Gazagnes ; S A Blecic ; D. Zegers De BeylPainful arm and moving fingers: clinical features of four new cases.
000978 (2003) Mark S. Ledoux [États-Unis] ; Kimberly A. BradySecondary cervical dystonia associated with structural lesions of the central nervous system.
000C71 (2003) Marina A J. Tijssen [Pays-Bas] ; Peter Brown ; David Macmanus ; Mary A. Mclean ; Charles DavieMagnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene.
001693 (2006) Feriha Ozer ; Hasan Meral ; Tuba Aydemir ; Oya OzturkHemiballism-Hemichorea in presentation of cranial tuberculoma.
001B59 (2007) Bart P C. Van De Warrenburg [Royaume-Uni] ; Carla Cordivari ; Peter Brown ; Kailash P. BhatiaPersisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy.
001D02 (2007) Yanush Sanotsky [Ukraine] ; Roman Lesyk ; Lyudmyla Fedoryshyn ; Iryna Komnatska ; Yuriy Matviyenko ; Stanley FahnManganic encephalopathy due to "ephedrone" abuse.
002061 (2008) Giacomina Rossi [Italie] ; Cecilia Marelli ; Laura Farina ; Matilde Laurà ; Anna Maria Basile ; Claudia Ciano ; Fabrizio Tagliavini ; Davide PareysonThe G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
002504 (2009) David Shprecher ; Roger KurlanThe Management of Tics
002691 (2009) Marcelo Galvez ; Javier Brahm ; Marcelo MirandaMovement disorders as a manifestation of metronidazole-induced encephalopathy in a patient with chronic liver disease.
002739 (2009) Robin Grant [Royaume-Uni] ; Francesc GrausParaneoplastic movement disorders.
002851 (2009) Jana Martinková ; Peter Valkovic ; Ján BenetinParaneoplastic chorea associated with breast cancer.
002A41 (2010) Meliha Tan ; Sibel Karaca ; Uner TanA new case of Uner Tan syndrome--with late childhood quadrupedalism.
002D48 (2010) Laura K. Teune [Pays-Bas] ; Anna L. Bartels ; Bauke M. De Jong ; Antoon T M. Willemsen ; Silvia A. Eshuis ; Jeroen J. De Vries ; Joost C H. Van Oostrom ; Klaus L. LeendersTypical cerebral metabolic patterns in neurodegenerative brain diseases.
002E25 (2010) Nune S. Yeghiazaryan ; Pasquale Striano ; Patrizia Accorsi ; Lorenzo Pinelli ; Francesca Faravelli ; Federico Zara ; Carlo Minetti ; Lucio GiordanoFamilial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?
002E57 (2011) M B Aerts [Pays-Bas] ; R A J. Esselink ; B R Bloem ; M M VerbeekCerebrospinal fluid tau and phosphorylated tau protein are elevated in corticobasal syndrome.
003224 (1990) A J Lewis [Canada] ; M J GawelDiffuse Lewy body disease with dementia and oculomotor dysfunction.

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