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
000263 (2000)	K P Bhatia ; R C Griggs ; L J Ptácek	Episodic movement disorders as channelopathies.
000285 (2000)	J J Higgins [États-Unis] ; K. Kluetzman ; J. Berciano ; O. Combarros ; J M Loveless	Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder.
000571 (2001)	C. Klein ; G S Stewart ; N P Quinn ; A M Taylor	Ataxia without telangiectasia revisited: update on genetic findings in two brothers with an ataxia-telangiectasia-like disorder.
000A49 (2003)	Melih Vural [Turquie] ; Sibel Ozekmekçi ; Hülya Apaydin ; Attila Altinel	High-dose piracetam is effective on cerebellar ataxia in patient with cerebellar cortical atrophy.
000B82 (2003)	Vicky Marshall [Royaume-Uni] ; Donald G. Grosset	Role of dopamine transporter imaging in the diagnosis of atypical tremor disorders.
000C75 (2003)	Susan H. Fox ; Anette Nieves ; Catherine Bergeron ; Anthony E. Lang	Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
000D36 (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.
000D37 (2004)	Johann M. Hagenah [Allemagne] ; Christine Zühlke ; Yorck Hellenbroich ; Wolfgang Heide ; Christine Klein	Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
000F63 (2004)	J. Benito-Le N [Espagne] ; J. Alvarez-Linera ; E D Louis	Neurosyphilis masquerading as corticobasal degeneration.
001370 (2005)	Niall P. Quinn [Royaume-Uni]	How to diagnose multiple system atrophy.
001418 (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.
001452 (1992)	R N Rosenberg	Machado-Joseph disease: an autosomal dominant motor system degeneration.
001453 (1992)	L. Sudarsky [États-Unis] ; L. Corwin ; D M Dawson	Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies.
001488 (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.
001569 (1991)	J. Vaamonde [Espagne] ; J. Artieda ; J A Obeso	Hereditary paroxysmal ataxia with neuromyotonia.
001598 (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.
001634 (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.
001965 (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.
001A75 (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.
002042 (2008)	Mona Ragothaman ; Uday Muthane	Homozygous SCA 2 mutations changes phenotype and hastens progression.
002108 (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.

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Ncbi/Checkpoint

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/Mesh.i -k "Spinocerebellar Degenerations" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/Mesh.i  \
                -Sk "Spinocerebellar Degenerations" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Ncbi
   |étape=   Checkpoint
   |type=    indexItem
   |index=    Mesh.i
   |clé=    Spinocerebellar Degenerations
}}

---

This area was generated with Dilib version V0.6.23. Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024