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Torsion dystonia in israel

✍ Scribed by Amos D. Korczyn; Esther Kahana; Nelly Zilber; Max Streifler; Raphael Carasso; Milton Alter


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
442 KB
Volume
8
Category
Article
ISSN
0364-5134

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πŸ“œ SIMILAR VOLUMES


Lithium therapy in torsion dystonia
✍ J. F. Marti-Masso; J. A. Obeso; N. Carrera; W. Astudillo; J. M. Martinez Lage πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 239 KB
Intrafamilial correlation in idiopathic
✍ Dr. N. A. Fletcher; A. E. Harding; C. D. Marsden πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 402 KB

Age of onset and severity of idiopathic torsion dystonia (ITD) were studied in 100 British families containing 107 index cases and 79 secondary cases. Analysis of variance of these clinical features did not suggest that ITD is genetically heterogenous, and they were similar in Jewish and non-Jewish

Laterality of onset in idiopathic torsio
✍ Rivka Inzelberg; Nelly Ziber; Esther Kahana; Prof. Amos D. Korczyn πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 378 KB

## Abstract Idiopathic torsion dystonia (ITD) is a dominantly inherited disorder with incomplete penetrance. It is important to identify factors that may cause dystonia or prevent its occurrence in a genetically predisposed individual. Because dystonia may be precipitated by peripheral triggers, we

Comparing endophenotypes in adult-onset
✍ David Bradley; Robert Whelan; Richard Walsh; John O'Dwyer; Richard Reilly; Siobh πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 113 KB

## Abstract Adult‐onset primary torsion dystonia (AOPTD) has an autosomal dominant pattern of inheritance with markedly reduced penetrance; the genetic causes of most forms of AOPTD remain unknown. Endophenotypes, markers of sub‐clinical gene carriage, may be of use detecting non‐manifesting gene c