## Abstract Fifty Japanese and European families with cortical myoclonic tremor and epilepsy have been reported under various names. Unfamiliarity with the syndrome often leads to an initial misdiagnosis of essential tremor or progressive myoclonus epilepsy. A detailed overview of the literature is
โฆ LIBER โฆ
Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy
โ Scribed by Antonio Suppa; Alfredo Berardelli; Francesco Brancati; Massimo Marianetti; Giuseppe Barrano; Concetta Mina; Antonio Pizzuti; Giulio Sideri
- Book ID
- 109111128
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2009
- Tongue
- English
- Weight
- 119 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0013-9580
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Familial cortical myoclonic tremor with
โ
Anne-Fleur Van Rootselaar; Ivo N. van Schaik; Arn M.J.M. van den Maagdenberg; Jo
๐
Article
๐
2005
๐
John Wiley and Sons
๐
English
โ 249 KB
Clinical and genetic analysis of a large
โ
Josรฉ M. Serratosa; Dr. Antonio V. Delgado-Escueta; Marco T. Medina; Quanwei Zhan
๐
Article
๐
1996
๐
John Wiley and Sons
๐
English
โ 891 KB
Clinical, pathological, and genetic feat
โ
Hisaomi Kawai; Masashi Akaike; Makoto Kunishige; Toshio Inui; Katsuhito Adachi;
๐
Article
๐
1998
๐
John Wiley and Sons
๐
English
โ 469 KB
๐ 3 views
We report on the clinical, pathological, and genetic features of 7 patients with limb-girdle muscular dystrophy type 2A (LGMD2A) from three Japanese families. The mean age of onset was 9.7 ยฑ 3.1 years (mean ยฑ SD), and loss of ambulance occurred at 38.5 ยฑ 2.1 years. Muscle atrophy was predominant in