Movement Disorders (revue) - Exploration (Accueil)

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List of bibliographic references indexed by quot

Number of relevant bibliographic references: 32.
[0-20] [0 - 20][0 - 32][20-31][20-40]
Ident.Authors (with country if any)Title
000088 (2015) Maja Kojovic [Royaume-Uni] ; Matteo Bologna [Italie] ; Mark J. Edwards [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]Reply to "Transcranial Magnetic Stimulation for Parkinson's Disease".
000332 (2015) Mika H. Martikainen [Royaume-Uni] ; Grainne S. Gorman [Royaume-Uni] ; Paul Goldsmith [Royaume-Uni] ; David J. Burn [Royaume-Uni] ; Doug M. Turnbull [Royaume-Uni] ; Andrew M. Schaefer [Royaume-Uni]Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation.
000379 (2014) Connie Marras [Canada] ; Alexander I. Tröster ; Jaime Kulisevsky ; Glenn T. StebbinsThe tools of the trade: a state of the art "How to Assess Cognition" in the patient with Parkinson's disease.
000625 (2014) Kishore R. Kumar [Australie] ; Christine KleinCommentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
000630 (2014) Mark Walterfang [Australie] ; Bart P. Van De WarrenburgCognitive impairment in "Other" movement disorders: hidden defects and valuable clues.
000691 (2014) Joseph Jankovic [États-Unis]"Psychogenic" versus "functional" movement disorders? That is the question.
000692 (2014) Stanley Fahn [États-Unis] ; C Warren Olanow"Psychogenic movement disorders": they are what they are.
000693 (2014) Paolo Calabresi [Italie] ; Veronica Ghiglieri"Lazy" nigrostriatal synapses in the heterozygous PINK1 mouse model of familial Parkinson's disease.
000803 (2013) Meike Kasten ; Birger Heinzow ; Peter Vieregge ; Christine KleinReply to: "polychlorinated biphenyls in prospectively collected serum and Parkinson's disease risk".
000858 (2013) Javier Blesa [États-Unis]Parkinson's disease: "Braak" to the future.
000A55 (2013) Maria Stamelou [Grèce]Commentary for "Slowing of saccadic eye movements in sporadic Creutzfeldt-Jakob disease".
000A56 (2013) Kailash P. Bhatia [Royaume-Uni]Commentary for "Progressive ataxia associated with scarring skin lesions and vertical gaze palsy".
000A57 (2013) Ruth H. Walker [États-Unis]Commentary for "Delayed onset of progressive chorea after acute basal ganglia injury".
000A58 (2013) Alberto J. Espay [États-Unis]Commentary for "Chediak-Higashi syndrome presenting as young-onset levodopa-responsive parkinsonism".
000A59 (2013) Christopher H. HawkesComment to letter: "Identical twins with LRRK2 mutation discordant for Parkinson's disease".
000B46 (2013) Michael R. Macaskill ; Daniel J. Myall ; Tim J. Anderson"Ocular tremor" in Parkinson's disease: a technology-dependent artifact of universal head motion?
000B47 (2013) Gerald Stern"Occam's razor" and identical twins with discordant Parkinson's Disease.
000B48 (2013) Maria Stamelou [Royaume-Uni] ; Niall P. Quinn ; Kailash P. Bhatia"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.
000C64 (2012) Andrew Lees [Royaume-Uni] ; Stanley Fahn ; Karla M. Eggert ; Joseph Jankovic [États-Unis] ; Anthony Lang ; Federico Micheli ; M Maral Mouradian ; Wolfgang H. Oertel ; C Warren Olanow ; Werner Poewe [Autriche] ; Olivier Rascol ; Eduardo Tolosa ; David Squillacote ; Dinesh KumarPerampanel, an AMPA antagonist, found to have no benefit in reducing "off" time in Parkinson's disease.
000E28 (2012) María T. Cáceres-Redondo ; Fátima Carrillo ; Francisco J. Palomar ; Pablo MirDYT-1 gene dystonic tremor presenting as a "scan without evidence of dopaminergic deficit".
000E36 (2012) Steven J. Frucht [États-Unis]Commentary on "Pallidopontonigral degeneration: a deceptive familial tauopathy".

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