Literature DB >> 9193167

The genetic basis of hereditary ataxia.

T Klockgether1, J Dichgans.   

Abstract

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Year:  1997        PMID： 9193167     DOI： 10.1016/s0079-6123(08)63387-7

Source DB:  PubMed          Journal:  Prog Brain Res        ISSN： 0079-6123            Impact factor:   2.453


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  7 in total

1.  Noninvasive detection of presymptomatic and progressive neurodegeneration in a mouse model of spinocerebellar ataxia type 1.

Authors:  Gülin Oz; Christopher D Nelson; Dee M Koski; Pierre-Gilles Henry; Malgorzata Marjanska; Dinesh K Deelchand; Ryan Shanley; Lynn E Eberly; Harry T Orr; H Brent Clark
Journal:  J Neurosci       Date:  2010-03-10       Impact factor: 6.167

2.  Enhanced neuronal excitability in the absence of neurodegeneration induces cerebellar ataxia.

Authors:  Vikram G Shakkottai; Chin-hua Chou; Salvatore Oddo; Claudia A Sailer; Hans-Günther Knaus; George A Gutman; Michael E Barish; Frank M LaFerla; K George Chandy
Journal:  J Clin Invest       Date:  2004-02       Impact factor: 14.808

3.  Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.

Authors:  Gülin Oz; Diane Hutter; Ivan Tkác; H Brent Clark; Myron D Gross; Hong Jiang; Lynn E Eberly; Khalaf O Bushara; Christopher M Gomez
Journal:  Mov Disord       Date:  2010-07-15       Impact factor: 10.338

4.  Sensitivity of Volumetric Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy to Progression of Spinocerebellar Ataxia Type 1.

Authors:  Dinesh K Deelchand; James M Joers; Adarsh Ravishankar; Tianmeng Lyu; Uzay E Emir; Diane Hutter; Christopher M Gomez; Khalaf O Bushara; Christophe Lenglet; Lynn E Eberly; Gülin Öz
Journal:  Mov Disord Clin Pract       Date:  2019-07-10

5.  Selenium levels and glutathione peroxidase activity in patients with ataxia-telangiectasia: association with oxidative stress and lipid status biomarkers.

Authors:  Itana Gomes Alves Andrade; Fabíola Isabel Suano-Souza; Fernando Luiz Affonso Fonseca; Carolina Sanchez Aranda Lago; Roseli Oselka Saccardo Sarni
Journal:  Orphanet J Rare Dis       Date:  2021-02-12       Impact factor: 4.123

6.  The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice.

Authors:  Corinna Lappe-Siefke; Sven Loebrich; Wulf Hevers; Oliver B Waidmann; Michaela Schweizer; Susanne Fehr; Jean-Marc Fritschy; Ivan Dikic; Jens Eilers; Scott M Wilson; Matthias Kneussel
Journal:  PLoS Genet       Date:  2009-09-04       Impact factor: 5.917

7.  Cerebrospinal Fluid Biomarkers in Spinocerebellar Ataxia: A Pilot Study.

Authors:  Ashley M Brouillette; Gülin Öz; Christopher M Gomez
Journal:  Dis Markers       Date:  2015-07-22       Impact factor: 3.434
  7 in total

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