✦ LIBER ✦

Spinocerebellar ataxia type 1 mimicking stiff person syndrome

✍ Scribed by Sumeet Singhal; Vamsi Gontu; Prajendra Choudhary; Dorothee Auer; Nin Bajaj

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 349 KB
Volume: 24
Category: Article
ISSN: 0885-3185
DOI: 10.1002/mds.22521

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Stiff man–like syndrome and generalized

Stiff man–like syndrome and generalized myokymia in spinocerebellar ataxia type 3

✍ José Berciano; Jon Infante; Antonio García; Carmen De Pablos; Guillermo Amer; Jo 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 156 KB

## Abstract We describe the novel association of spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) phenotype combining classical clinical presentation and semeiology mimicking stiff man syndrome (SMS). The studied pedigree comprises seven affected members in three generations. Their c

Acute ataxia, Graves' disease, and stiff

Acute ataxia, Graves' disease, and stiff person syndrome

✍ Su-Ynn Chia; Richard Chua; Yew-Long Lo; Meng-Cheong Wong; Ling-Ling Chan; Eng-Ki 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB

## Abstract Stiff person syndrome (SPS) has been associated with autoimmune diseases, such as Type 1 diabetes mellitus and autoimmune thyroid disease (Hashimoto's thyroiditis), among others. The association of SPS with hyperthyroidism is extremely rare. We describe a patient with uncontrolled Grave

Frequency of spinocerebellar ataxia type

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia

✍ Storey, Elsdon ;du Sart, Desiree ;Shaw, Janet H. ;Lorentzos, Peter ;Kelly, Louis 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 263 KB 👁 2 views

Dystonia as a presenting sign of spinoce

Dystonia as a presenting sign of spinocerebellar ataxia type 1

✍ Yih-Ru Wu; Guey-Jen Lee-Chen; Anthony E. Lang; Chiung-Mei Chen; Hsuan-Yuan Lin; 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 514 KB

## Abstract We report on a 39‐year‐old man who presented initially with marked blepharospasm, oromandibular dystonia and retrocollis and one year later developed mild ataxia. Our findings suggest that dystonia can be a disabling presenting sign of SCA1 and support the clinical heterogeneity of SCA1

Motor evoked potentials in the spinocere

Motor evoked potentials in the spinocerebellar ataxias type 1 and type 3

✍ Ludger Schöls; Georgios Amoiridis; Mathias Langkafel; Stephan Schöls; Horst Przu 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 45 KB

Autosomal dominant cerebellar ataxias (ADCA) are a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by progressive cerebellar ataxia and a varying combination of pyramidal and extrapyramidal signs, peripheral neuropathy, external ophthalmoplegia, and dyspha

Early symptoms in spinocerebellar ataxia

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

✍ Christoph Globas; Sophie Tezenas du Montcel; Laslo Baliko; Syliva Boesch; Chanta 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB

## Abstract Onset of genetically determined neurodegenerative diseases is difficult to specify because of their insidious and slowly progressive nature. This is especially true for spinocerebellar ataxia (SCA) because of varying affection of many parts of the nervous system and huge variability of