Movement Disorders (revue) - Curation (Ncbi)

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List of bibliographic references

Number of relevant bibliographic references: 354.
[0-20] [0 - 20][0 - 50][20-40]
Ident.Authors (with country if any)Title
000079 (1999) J M Errea [Espagne] ; J R Ara ; C. Aibar ; J. De Pedro-CuestaPrevalence of Parkinson's disease in lower Aragon, Spain.
000087 (1999) S. Nagamitsu [Japon] ; T. Matsuishi ; K. Hashimoto ; Y. Yamashita ; M. Aihara ; K. Shimizu ; M. Mizuguchi ; H. Iwamoto ; S. Saitoh ; Y. Hirano ; H. Kato ; Y. Fukuyama ; M. ShimadaMulticenter study of paroxysmal dyskinesias in Japan--clinical and pedigree analysis.
000091 (1999) C. Kamm [Allemagne] ; E. Castelon-Konkiewitz ; M. Naumann ; F. Heinen ; M. Brack ; A. Nebe ; A. Ceballos-Baumann ; T. GasserGAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
000131 (1999) T. Pohle [Suisse] ; J K KraussParkinsonism in children resulting from mesencephalic tumors.
000141 (1999) E A Sekul [États-Unis] ; S. Kaminer ; K D SethiDigoxin-induced chorea in a child.
000150 (1999) M W Hayes [Australie] ; S. Graham ; P. Heldorf ; G. De Moore ; J G MorrisA video review of the diagnosis of psychogenic gait: appendix and commentary.
000162 (1999) D L Picchietti [États-Unis] ; D J Underwood ; W A Farris ; A S Walters ; M M Shah ; R E Dahl ; L J Trubnick ; M A Bertocci ; M. Wagner ; W A HeningFurther studies on periodic limb movement disorder and restless legs syndrome in children with attention-deficit hyperactivity disorder.
000167 (1999) P. Bonanni [Italie] ; R. GuerriniSegmental facial myoclonus in moebius syndrome.
000177 (1999) M S Lee [Corée du Sud] ; Y D Kim ; W C Kim ; C H LyooSlow rhythmic dyskinesia of the shoulder: one idopathic and two symptomatic cases.
000226 (2000) A. Schrag [Royaume-Uni] ; N P Quinn ; K P Bhatia ; C D MarsdenBenign hereditary chorea--entity or syndrome?
000254 (2000) S. Frucht [États-Unis] ; S. FahnThe clinical spectrum of posthypoxic myoclonus.
000280 (2000) P E Greene [États-Unis] ; S B Bressman ; B. Ford ; K. HylandParkinsonism, dystonia, and hemiatrophy.
000283 (2000) F. Alarc N ; G. Due As ; N. Cevallos ; A J LeesMovement disorders in 30 patients with tuberculous meningitis.
000284 (2000) M A Beran-Koehn [États-Unis] ; M L Zupanc ; M C Patterson ; D G Olk ; J E AhlskogViolent recurrent ballism associated with infections in two children with static encephalopathy.
000285 (2000) J J Higgins [États-Unis] ; K. Kluetzman ; J. Berciano ; O. Combarros ; J M LovelessPosterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder.
000387 (2000) J. Kalita [Inde] ; U K MisraMarkedly severe dystonia in Japanese encephalitis.
000389 (2000) D M Sheppard [Royaume-Uni] ; J L Bradshaw ; N. Georgiou ; J A Bradshaw ; P. LeeMovement sequencing in children with Tourette's syndrome and attention deficit hyperactivity disorder.
000402 (2000) A. Filla [Italie] ; G. De Michele ; G. Coppola ; A. Federico ; G. Vita ; A. Toscano ; A. Uncini ; P. Pisanelli ; P. Barone ; V. Scarano ; A. Perretti ; L. Santoro ; A. Monticelli ; F. Cavalcanti ; G. Caruso ; S. CocozzaAccuracy of clinical diagnostic criteria for Friedreich's ataxia.
000423 (2001) D A Grimes [Canada] ; D. Bulman ; P S George-Hyslop ; A E LangInherited myoclonus-dystonia: evidence supporting genetic heterogeneity.
000425 (2001) J. Shahed [États-Unis] ; Joseph Jankovic [États-Unis]Re-emergence of childhood stuttering in Parkinson's disease: a hypothesis.
000492 (2001) C. Yalçinkaya [Turquie] ; H. Apaydin ; S. Ozekmekçi ; K M GibsonDelayed-onset dystonia associated with 3-oxothiolase deficiency.

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