𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prospective study of peripheral neuropathy in Machado–Joseph disease

✍ Scribed by Marcondes C. França Jr.; Anelyssa D'abreu; Anamarli Nucci; Fernando Cendes; Iscia Lopes-Cendes


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
118 KB
Volume
40
Category
Article
ISSN
0148-639X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Progression of ataxia in patients with M
✍ Marcondes C. França Jr; Anelyssa D'Abreu; Anamarli Nucci; Fernando Cendes; Iscia 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

## Abstract Although ataxia is the most distressing manifestation of Machado‐Joseph disease (MJD), little is known about its natural history. Therefore, we prospectively followed a cohort of patients with MJD for 13 months to characterize the progression of ataxia and identify its contributory fact

Dopaminergic response in Parkinsonian ph
✍ Carsten Buhmann; Alexandra Bussopulos; Matthias Oechsner 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 125 KB

## 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 diff

Ethnic differences in the expression of
✍ S.H. Subramony; Dena Hernandez; Amanda Adam; Stephanie Smith-Jefferson; Jennifer 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 65 KB

## Abstract We describe several families of African origin with SCA3/Machado‐Joseph disease gene expansions. In these cases, the phenotype ranges from ataxia with parkinsonian signs to a syndrome clinically almost indistinguishable from idiopathic, L‐dopa–responsive Parkinson's disease. In contrast

Autonomic and peripheral (sensorimotor)
✍ Vinay Chaudhry; Andrea M. Corse; Richard O'Brian; David R. Cornblath; Andrew S. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB

Peripheral neuropathy has been reported in association with chronic liver disease. However, the precise incidence, severity and characteristics of neuropathy, and the relationship of neuropathy to different etiologies of liver disease have not been defined. In this study, 58 patients with advanced l

Somatic mosaicism of the CAG repeat expa
✍ Géraldine Cancel; Isabelle Gourfinkel-An; Giovanni Stevanin; Olivier Didierjean; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB 👁 1 views

An expanded and unstable CAG repeat in the coding region of the MJD1 gene is the mutation responsible for spinocerebellar ataxia 3/Machado-Joseph disease. In order to determine whether there was a higher degree of instability in affected regions, the size of the expanded CAG repeat was analyzed in d