Astrocytoma < Ataxia < Ataxia Telangiectasia

Facettes :

List of bibliographic references indexed by Ataxia

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

Ident.	Authors (with country if any)	Title
000261 (2015)	Brent L. Fogel [États-Unis] ; Sonya M. Hanson ; Esther B E. Becker	Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
000383 (2014)	Christos Ganos [Allemagne] ; Panagiotis Kassavetis ; Roberto Erro ; Mark J. Edwards ; John Rothwell ; Kailash P. Bhatia	The role of the cerebellum in the pathogenesis of cortical myoclonus.
000533 (2014)	Karen M. Doherty [Royaume-Uni] ; Thomas T. Warner ; Andrew J. Lees	Late onset ataxia: MSA-C or SCA 17? A gene penetrance dilemma.
000585 (2014)	Carlos Hernández-Lahoz [Espagne] ; Luis Rodrigo-Sáez ; Juan Vega-Villar ; Gerard Mauri-Capdevila ; Jorge Mier-Juanes	Familial gluten ataxia.
000622 (2014)	Maria Stamelou [Royaume-Uni]	Commentary.
000624 (2014)	José Berciano [Espagne]	Commentary.
000824 (2013)	Christos Ganos [Allemagne] ; Saskia Biskup ; Stefanie Kleinmichel ; Simone Zittel ; Odette Schunke ; Christian Gerloff ; Alexander Münchau	Progressive ataxia associated with scarring skin lesions and vertical gaze palsy.
000825 (2013)	Maria Stamelou [Royaume-Uni] ; Matthew Adams [Royaume-Uni] ; Indran Davagnanam [Royaume-Uni] ; Amit Batla [Royaume-Uni] ; Una Sheerin [Royaume-Uni] ; Kevin Talbot [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Progressive ataxia and palatal tremor associated with dense pontine calcification: A unique case
000899 (2013)	Michael C. Kruer [États-Unis] ; Tyler N. Jepperson ; Jill M. Weimer ; Amy Mroch ; Laura Davis-Keppen ; Patricia Crotwell ; Jillian Parboosingh	Mutations in VLDLR associated with ataxia with secondary vitamin E deficiency.
000903 (2013)	Wilhelmina G. Leen [Pays-Bas] ; Leena Mewasingh ; Marcel M. Verbeek ; Erik-Jan Kamsteeg ; Bart P. Van De Warrenburg ; Michel A. Willemsen	Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
000941 (2013)	Jennifer Müller Vom Hagen [Allemagne] ; Matthis Synofzik ; Julia Schicks ; Ingeborg Kr Geloh-Mann ; Ludger Schöls	Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
000A56 (2013)	Kailash P. Bhatia [Royaume-Uni]	Commentary for "Progressive ataxia associated with scarring skin lesions and vertical gaze palsy".
000B60 (2012)	Suhan Senova ; Béchir Jarraya ; Hiro Iwamuro ; Naoki Tani ; Naoufel Ouerchefani ; Hélène Lepetit ; Jean-Marc Gurruchaga ; Pierre Brugières ; Emmanuelle Apartis ; Thomas De Broucker ; Stéphane Palfi	Unilateral thalamic stimulation safely improved fragile X-associated tremor ataxia: a case report.
000B66 (2012)	Tao Xie ; Robert Goodman ; Nina Browner ; Elizabeth Haberfeld ; Linda Winfield ; Jill Goldman ; Blair Ford	Treatment of fragile X-associated tremor/ataxia syndrome with unilateral deep brain stimulation.
000C24 (2012)	Ana L. Pelayo-Negro ; Coro Sánchez-Quintana ; Maria C. Rodríguez-Oroz ; Victor Volpini ; Massimo Zeviani ; Miguel A. Tola-Arribas ; José Berciano ; Jon Infante	Screening for POLG W748S and A467T mutations in ataxia patients from Spain.
000C48 (2012)	Ammar Kheder [Royaume-Uni] ; Stuart Currie ; Charles Romanowski ; Marios Hadjivassiliou	Progressive ataxia with palatal tremor due to gluten sensitivity.
000F08 (2012)	Shinsuke Fujioka ; Sruti Rayaprolu ; Christina Sundal ; Daniel F. Broderick ; William A. Langley ; John Shoffner ; Lauren C. Hyams ; Rosa Rademakers ; Neill R. Graff-Radford ; William Tatum ; Owen A. Ross ; Zbigniew K. Wszolek	A novel de novo pathogenic mutation in CACNA1A gene
000F12 (2012)	Rosa Guerrero-L Pez ; Pedro J. García-Ruiz ; Beatriz G. Giráldez ; Carmen Durán-Herrera ; Maria Rosa Querol-Pascual ; José María Ramírez-Moreno ; Sebastián Más ; José M. Serratosa	A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.
000F29 (2012)	Maja Kojovic [Royaume-Uni] ; Una-Marie Sheerin [Royaume-Uni] ; Ignacio Rubio-Agusti [Royaume-Uni] ; Anirban Saha [Royaume-Uni] ; Jose Bras [Royaume-Uni] ; Vaneesha Gibbons [Royaume-Uni] ; Rodger Palmer [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Young-Onset Parkinsonism due to Homozygous Duplication of α-Synuclein in a Consanguineous Family
001045 (2012)	Jorge L. Juncos [États-Unis] ; Joash T. Lazarus [États-Unis] ; Julia Rohr [États-Unis] ; Emily G. Allen [États-Unis] ; Lisa Shubeck [États-Unis] ; Debra Hamilton [États-Unis] ; Gloria Novak [États-Unis] ; Stephanie L. Sherman [États-Unis]	Olfactory Dysfunction in Fragile X Tremor Ataxia Syndrome
001260 (2011)	Deborah Hall [États-Unis] ; Flora Tassone [États-Unis] ; Olga Klepitskaya [États-Unis] ; Maureen Leehey [États-Unis]	Fragile X-Associated Tremor Ataxia Syndrome in FMR1 Gray Zone Allele Carriers

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