Astrocytoma < Ataxia < Ataxia Telangiectasia

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List of bibliographic references

Number of relevant bibliographic references: 76.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000034 (1999)	M. Onofrj [Italie] ; A. Thomas	Acetazolamide-responsive periodic ataxia induced by amiodarone.
000192 (2000)	F. Stocchi [Italie] ; D. Badiali ; L. Vacca ; L. D'Alba ; F. Bracci ; S. Ruggieri ; M. Torti ; A. Berardelli ; E. Corazziari	Anorectal function in multiple system atrophy and Parkinson's disease.
000239 (2000)	B. Okuda [Japon] ; N. Kodama ; H. Tachibana ; M. Sugita ; H. Tanaka	Visuomotor ataxia in corticobasal degeneration.
000594 (2001)	P J Hand [Australie] ; R J Gardner ; M A Knight ; S M Forrest ; E. Storey	Clinical features of a large Australian pedigree with episodic ataxia type 1.
000834 (2002)	Miriam Vélez [Pérou] ; Carlos Cosentino ; Luis Torres	Levodopa-responsive rubral (Holmes') tremor.
000A46 (2003)	Jay C. Erickson [États-Unis] ; Bahman Jabbari ; Marc P. Difazio	Basal ganglia injury as a complication of the ketogenic diet.
000E67 (2004)	Kevin C. Engel [États-Unis] ; John H. Anderson ; Christopher M. Gomez ; John F. Soechting	Deficits in ocular and manual tracking due to episodic ataxia type 2.
001071 (2005)	Kenju Hara [Japon] ; Osamu Onodera ; Minoru Endo ; Hiroshi Kondo ; Hiroshi Shiota ; Kenji Miki ; Naoyuki Tanimoto ; Tetsuya Kimura ; Masatoyo Nishizawa	Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in Japan.
001195 (2005)	Anelyssa D'Abreu [États-Unis] ; Joseph Friedman ; Jim Coskun	Non-movement disorder heralds symptoms of Machado-Joseph disease years before ataxia.
001281 (2005)	James H. Bower [États-Unis] ; Mesfin Teshome ; Zenebe Melaku ; Guta Zenebe	Frequency of movement disorders in an Ethiopian university practice.
001325 (2005)	Chiara Criscuolo [Italie] ; Francesco Saccà ; Giuseppe De Michele ; Pietro Mancini ; Onofre Combarros ; Jon Infante ; Antonio Garcia ; Sandro Banfi ; Alessandro Filla ; José Berciano	Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia.
001355 (2005)	Parastoo Momeni [États-Unis] ; Chin-Song Lu ; Yah-Huei Wu Chou ; Hsiu-Chen Chang ; Rou-Shayn Chen ; Chiung-Chu Chen ; Jin-Tian Hsu ; Andrew Singleton ; John Hardy	Taiwanese cases of SCA2 are derived from a single founder.
001429 (2006)	Anna De Rosa [Italie] ; Pasquale Striano ; Fabrizio Barbieri ; Arturo De Falco ; Carlo Rinaldi ; Tecla Tucci ; Salvatore Striano ; Alessandro Filla ; Giuseppe De Michele	Suppression of myoclonus in SCA2 by piracetam.
001968 (2007)	Maureen A. Leehey [États-Unis] ; Elizabeth Berry-Kravis ; Sung-Joon Min ; Deborah A. Hall ; Cathlin D. Rice ; Lin Zhang ; Jim Grigsby ; Claudia M. Greco ; Ann Reynolds ; Rebecca Lara ; Jennifer Cogswell ; Sebastien Jacquemont ; David R. Hessl ; Flora Tassone ; Randi Hagerman ; Paul J. Hagerman	Progression of tremor and ataxia in male carriers of the FMR1 premutation.
001986 (2007)	Michael Abele [Allemagne] ; Thomas Klockgether	Health-related quality of life in sporadic adult-onset ataxia.
001998 (2007)	Steven A. Gunzler [États-Unis] ; A Jon Stoessl ; Robert A. Egan ; Richard G. Weleber ; Paul Wang ; John G. Nutt	Joubert syndrome surviving to adulthood associated with a progressive movement disorder.
001A62 (2007)	Chul H. Lyoo [Corée du Sud] ; Seung Yeob Lee ; Tae Jin Song ; Myung Sik Lee	Abnormal temporal discrimination threshold in patients with multiple system atrophy.
001B63 (2007)	Alon Abraham ; Cogan Elena ; Eldad Melamed ; Ruth Djaldetti	Successful treatment of truncal myoclonus.
001C20 (2007)	Kenju Hara ; Junsuke Shimbo ; Hiroaki Nozaki ; Koki Kikugawa ; Osamu Onodera ; Masatoyo Nishizawa	Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.
001C42 (2007)	Anja Weyer [Allemagne] ; Michael Abele ; Tanja Schmitz-Hübsch ; Beate Schoch ; Markus Frings ; Dagmar Timmann ; Thomas Klockgether	Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients.
001C43 (2007)	Judit Horvath ; Pierre R. Burkhard ; Michael Morris ; Armand Bottani ; Isabelle Moix ; Jacqueline Delavelle	Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case.

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