Literature DB >> 12539220

Dopaminergic response in Parkinsonian phenotype of Machado-Joseph disease.

Carsten Buhmann1, Alexandra Bussopulos, Matthias Oechsner.   

Abstract

We report on a patient with genetically proven Machado-Joseph Disease (MJD) presenting with signs indistinguishable from Parkinson's disease (PD), including levodopa response and typical levodopa-induced motor fluctuations. Only after 10 years of prolonged benefit from levodopa and different dopamine agonists (DA), the patient developed cerebellar ataxia and pyramidal signs. Preferential D3-receptor-stimulating dopamine agonists especially showed a benefit at the time, when D2 receptor binding was reduced in IBZM SPECT. This is the first report of a meaningful response to DA in MJD. Copyright 2002 Movement Disorder Society

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12539220     DOI: 10.1002/mds.10322

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  12 in total

Review 1.  Tremor-spectrum in spinocerebellar ataxia type 3.

Authors:  Cecilia Bonnet; Emmanuelle Apartis; Mathieu Anheim; Andre P Legrand; Jose F Baizabal-Carvallo; Anne M Bonnet; Alexandra Durr; Marie Vidailhet
Journal:  J Neurol       Date:  2012-05-17       Impact factor: 4.849

Review 2.  Machado-Joseph Disease: from first descriptions to new perspectives.

Authors:  Conceição Bettencourt; Manuela Lima
Journal:  Orphanet J Rare Dis       Date:  2011-06-02       Impact factor: 4.123

Review 3.  Machado-Joseph disease/spinocerebellar ataxia type 3.

Authors:  Henry Paulson
Journal:  Handb Clin Neurol       Date:  2012

Review 4.  Role of ubiquitin-proteasome-mediated proteolysis in nervous system disease.

Authors:  Ashok N Hegde; Sudarshan C Upadhya
Journal:  Biochim Biophys Acta       Date:  2010-08-03

Review 5.  Machado-Joseph disease in a Nigerian family: mutational origin and review of the literature.

Authors:  Shamsideen Abayomi Ogun; Sandra Martins; Philip B Adebayo; Clara O Dawodu; Jorge Sequeiros; Michael F Finkel
Journal:  Eur J Hum Genet       Date:  2014-04-30       Impact factor: 4.246

6.  Expanded and Wild-type Ataxin-3 Modify the Redox Status of SH-SY5Y Cells Overexpressing α-Synuclein.

Authors:  Carolina Noronha; Rita Perfeito; Mário Laço; Ullrich Wüllner; A Cristina Rego
Journal:  Neurochem Res       Date:  2017-02-25       Impact factor: 3.996

7.  Spinocerebellar ataxia type 3: response to levodopa infusion in two cases.

Authors:  Javier Miranda; Esther Cubo
Journal:  Neurol Sci       Date:  2022-02-24       Impact factor: 3.830

Review 8.  SCA3: neurological features, pathogenesis and animal models.

Authors:  Olaf Riess; Udo Rüb; Annalisa Pastore; Peter Bauer; Ludger Schöls
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

9.  Striatal dopamine depletion induces forelimb motor impairments and disrupts forelimb movement representations within the motor cortex.

Authors:  Emily K Plowman; Nagheme J Thomas; Jeffrey A Kleim
Journal:  J Parkinsons Dis       Date:  2011       Impact factor: 5.568

10.  Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.

Authors:  Conceição Bettencourt; Cristina Santos; Paula Coutinho; Patrizia Rizzu; João Vasconcelos; Teresa Kay; Teresa Cymbron; Mafalda Raposo; Peter Heutink; Manuela Lima
Journal:  BMC Neurol       Date:  2011-10-24       Impact factor: 2.474

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.