Spinocerebellar Ataxias < Spinocerebellar Degenerations < Spiperone

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 48.
[0-20] [0 - 20][0 - 48][20-40]

Ident.	Authors (with country if any)	Title
000836 (2013)	Judith Van Gaalen [Pays-Bas] ; Sascha Vermeer ; Marjon Van Veluw ; Bart P C. Van De Warrenburg ; Dennis Dooijes	A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia.
000B20 (2012)	Steven Frucht [États-Unis]	Commentary for "oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8".
000B21 (2012)	Mwiza Ushe [États-Unis] ; Joel S. Perlmutter	Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.
001B62 (2009)	Günther Deuschl [Allemagne] ; Rodger Elble	Essential tremor--neurodegenerative or nondegenerative disease towards a working definition of ET.
001D43 (2009)	M Mar Trujillo-Martín [Espagne] ; Pedro Serrano-Aguilar ; Fernando Monton-Alvarez ; Romen Carrillo-Fumero	Effectiveness and safety of treatments for degenerative ataxias: a systematic review.
001F44 (2009)	Marianna Amboni ; Maria Teresa Pellecchia ; Autilia Cozzolino ; Marina Picillo ; Carmine Vitale ; Paolo Barone ; Andrea Varrone ; Barbara Garavaglia ; Simona Gambelli ; Antonio Federico	Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK-2.
002171 (2008)	Catherine C S. Delnooz ; Jurgen H. Schelhaas ; Bart P C. Van De Warrenburg ; Robert-Jan De Graaf ; Gajja S. Salomons	Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs.
002185 (2008)	Juan Fortea ; Yaroslau Compta ; Francesc Valldeoriola ; Eduardo Tolosa ; Yaroslau Compta ; María Jesús Rey ; Teresa Ribalta ; Félix Gast N ; Teresa Ribalta	Fatal worsening of late-onset cerebellar ataxia with neuronal intranuclear inclusions due to superimposed meningeal Rosai-Dorfman disease.
002195 (2008)	Joong-Seok Kim ; Jae-Young An ; Kwang-Soo Lee ; Yong-An Chung ; Jin-Soo Choi ; Kwon-Haeng Lee	PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome.
002253 (2008)	Shigeki Hirano [Japon] ; Hitoshi Shinotoh ; Kimihito Arai ; Akiyo Aotsuka ; Fumihiko Yasuno ; Noriko Tanaka ; Tsuneyoshi Ota ; Koichi Sato ; Kiyoshi Fukushi ; Shuji Tanada ; Takamichi Hattori ; Toshiaki Irie	PET study of brain acetylcholinesterase in cerebellar degenerative disorders.
002317 (2008)	Mona Ragothaman ; Uday Muthane	Homozygous SCA 2 mutations changes phenotype and hastens progression.
002864 (2007)	Jim Grigsby [États-Unis] ; Angela G. Brega ; Maureen A. Leehey ; Glenn K. Goodrich ; Sébastien Jacquemont ; Danuta Z. Loesch ; Jennifer B. Cogswell ; Jennifer Epstein ; Rebecca Wilson ; Tristan Jardini ; Emma Gould ; Rachael E. Bennett ; David Hessl ; Susannah Cohen ; Kylee Cook ; Flora Tassone ; Paul J. Hagerman ; Randi J. Hagerman	Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome.
002974 (2007)	Thomas Eckert [États-Unis] ; Andrew Feigin ; Daniel E. Lewis ; Vijay Dhawan ; Steven Frucht ; David Eidelberg	Regional metabolic changes in parkinsonian patients with normal dopaminergic imaging.
002C97 (2006)	E K Tan [Singapour] ; Lisa Skipper ; Eva Chua ; Meng-Cheong Wong ; Ratnagopal Pavanni ; Carine Bonnard ; Prasanna Kolatkar ; Jian-Jun Liu	Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.
002D33 (2006)	Davide Martino [Royaume-Uni] ; Nee-Kong Chew ; Pablo Mir ; Mark J. Edwards ; Niall P. Quinn ; Kailash P. Bhatia	Atypical movement disorders in antiphospholipid syndrome.
002E40 (2006)	Esther Brusse [Pays-Bas] ; Inge De Koning ; Anneke Maat-Kievit ; Ben A. Oostra ; Peter Heutink ; John C. Van Swieten	Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
002E94 (2006)	Nils Peters [Allemagne] ; Christoph Kamm ; Friedrich Asmus ; Elke Holinski-Feder ; Eduard Kraft ; Martin Dichgans ; Roland Brüning ; Thomas Gasser ; Kai Bötzel	Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
002F42 (2005)	Niall P. Quinn [Royaume-Uni]	How to diagnose multiple system atrophy.
003325 (2004)	J. Benito-Le N [Espagne] ; J. Alvarez-Linera ; E D Louis	Neurosyphilis masquerading as corticobasal degeneration.
003547 (2004)	Johann M. Hagenah [Allemagne] ; Christine Zühlke ; Yorck Hellenbroich ; Wolfgang Heide ; Christine Klein	Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
003548 (2004)	Anne-Fleur Van Rootselaar [Pays-Bas] ; Eleonora Aronica ; Ernst N H. Jansen Steur ; Johanna M. Rozemuller-Kwakkel ; Rob A I. De Vos ; Marina A J. Tijssen	Familial cortical tremor with epilepsy and cerebellar pathological findings.

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