Astrocytoma < Ataxia < Ataxia Telangiectasia

Facettes :

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
000325 (2015)	Brent L. Fogel ; Sonya M. Hanson ; Esther B E. Becker	Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
000550 (2014)	Maria Stamelou	Commentary.
000551 (2014)	Christos Ganos ; Panagiotis Kassavetis ; Roberto Erro ; Mark J. Edwards ; John Rothwell ; Kailash P. Bhatia	The role of the cerebellum in the pathogenesis of cortical myoclonus.
000628 (2014)	Carlos Hernández-Lahoz ; Luis Rodrigo-Sáez ; Juan Vega-Villar ; Gerard Mauri-Capdevila ; Jorge Mier-Juanes	Familial gluten ataxia.
000645 (2014)	José Berciano	Commentary.
000653 (2014)	Karen M. Doherty ; Thomas T. Warner ; Andrew J. Lees	Late onset ataxia: MSA-C or SCA 17? A gene penetrance dilemma.
000787 (2013)	Jennifer Müller Vom Hagen ; Matthis Synofzik ; Julia Schicks ; Ingeborg Kr Geloh-Mann ; Ludger Schöls	Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
000858 (2013)	Michael C. Kruer ; 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.
000865 (2013)	Wilhelmina G. Leen ; 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.
000950 (2013)	Kailash P. Bhatia	Commentary for "Progressive ataxia associated with scarring skin lesions and vertical gaze palsy".
000951 (2013)	Christos Ganos ; Saskia Biskup ; Stefanie Kleinmichel ; Simone Zittel ; Odette Schunke ; Christian Gerloff ; Alexander Münchau	Progressive ataxia associated with scarring skin lesions and vertical gaze palsy.
000A17 (2013)	Maria Stamelou ; Matthew Adams ; Indran Davagnanam ; Amit Batla ; Una Sheerin ; Kevin Talbot ; Kailash P. Bhatia	Progressive ataxia and palatal tremor associated with dense pontine calcification: A unique case.
000B43 (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.
000B44 (2012)	Bradley Osterman ; Michel Sylvain ; Sylvain Chouinard ; Geneviève Bernard	Tremor-ataxia with central hypomyelination (TACH): dystonia as a new clinical feature.
000C05 (2012)	Jorge L. Juncos ; Joash T. Lazarus ; Julia Rohr ; Emily G. Allen ; Lisa Shubeck ; Debra Hamilton ; Gloria Novak ; Stephanie L. Sherman	Olfactory dysfunction in fragile X tremor ataxia syndrome.
000C10 (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 the CACNA1A gene.
000D36 (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.
000E52 (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.
000E82 (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.
000E94 (2012)	Ammar Kheder ; Stuart Currie ; Charles Romanowski ; Marios Hadjivassiliou	Progressive ataxia with palatal tremor due to gluten sensitivity.
000F43 (2012)	Deborah Hall ; Flora Tassone ; Olga Klepitskaya ; Maureen Leehey	Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriers.

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