𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multiple sclerosis presenting as adult onset dystonia

✍ Scribed by Dr. R. J. Coleman; N. P. Quinn; C. D. Marsden


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
271 KB
Volume
3
Category
Article
ISSN
0885-3185

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Sporadic rapid-onset dystonia–parkinsoni
✍ Daan J. Kamphuis; Hans Koelman; Andrew J. Lees; Marina A.J. Tijssen 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 46 KB 👁 1 views

## Abstract We report on a 38‐year‐old patient with rapid‐onset dystonia–parkinsonism (RDP) with a missense mutation in the Na/K‐ATPase α3 subunit (ATP1A3). Asymmetrical parkinsonian symptoms evolved over a year. After a stable episode of another 2.5 years, overnight he developed oromandibular dyst

Laryngeal dystonia as a presenting sympt
✍ Spiridon Papapetropoulos; Donna S. Lundy; Roy R. Casiano; Carlos Singer 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 44 KB 👁 1 views

Echocardiogram revealed diffuse hypokinesis, dilatation of left ventricular cavity, and thinning of left ventricular wall. Ejection fraction was decreased to 49%. Cardiac muscle biopsy demonstrated hypertrophied cardiomyocyte and interstitial fibrosis of left ventricle. A gastrocnemius muscle biopsy

Paroxysmal exercise-induced dystonia as
✍ Maria Bozi; Kailash P. Bhatia 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 52 KB 👁 1 views

## Abstract Paroxysmal exercise‐induced dystonia (PED) is a rare, typically idiopathic familial condition, although sporadic and secondary cases have been reported. We present 2 cases where PED was the presenting feature of young‐onset idiopathic Parkinson's disease (PD), preceding the onset of par

Congenital disorder of glycosylation typ
✍ Kerrie L. Schoffer; John D. O'Sullivan; Jim McGill 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 92 KB

## Abstract Congenital disorders of glycosylation (CDG) are a recently described, underrecognized group of syndromes characterized biochemically by abnormal glycosylation of serum and cellular glycoproteins. We report a previously undiagnosed adult male who presented with early‐onset cerebellar ata