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pro vyhledávání: '"G, Amoiridis"'
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Publikováno v:
Brain. 120:2131-2140
Friedreich's ataxia is an autosomal recessively inherited neurodegenerative disorder caused by expansions of an unstable GAA trinucleotide repeat in the STM7/X25 gene on chromosome 9q. We studied the (GAA)n polymorphism in 178 healthy controls and 10
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 65:79-89
Hereditary ataxias are a heterogeneous group of neurodegenerative diseases. Neither the clinical features nor the findings at autopsy provide a satisfactory basis for the isolation of distinct categories and classification. Recently, several gene loc
Autor:
E. S. Ganotakis, Joanna Moschandrea, Miltiadis K. Tsilimbaris, E. Nitoda, A. Pallikaris, G. Amoiridis, P. Kallinikos
Publikováno v:
Current eye research. 37(10)
To employ corneal confocal microscopy to assess differences in the extent of corneal nerve fiber alterations between diabetic patients classed according to retinopathy status and nondiabetic patients.Two hundred seventy-eight corneas of 139 patients
Publikováno v:
Acta Ophthalmologica. 88
Purpose Corneal confocal microscopy is a rapid, non-invasive and reiterative technique, suitable for the accurate detection and quantification of corneal subbasal nerve plexus. The aim of this study is to correlate corneal nerve fibre alterations wit
Autor:
G. Amoiridis, J. Haan
Publikováno v:
Klinische Neurophysiologie. 21:51-55
Proximal and distal latency as well as motor nerve conduction velocity were determined in the following nerves in 100 subjects (71 healthy subjects and 29 patients): tibial, peroneal, ulnar, median. All neurographic parameters were obtained by means
Publikováno v:
Annals of neurology. 42(6)
Seventy-seven families with autosomal dominant cerebellar ataxia were analyzed for the CAG repeat expansions causing spinocerebellar ataxia (SCA) types 1, 2, 3, and 6. The SCA1 mutation accounted for 9%, SCA2 for 10%, SCA3 for 42%, and SCA6 for 22% o
Publikováno v:
Electromyography and clinical neurophysiology. 37(5)
We report the case of a 40 year-old man with a severe lesion of the anterior rami of the left spinal nerves L5 and S1 who showed hypertrophy of the leg and atrophy of the intrinsic foot and gluteal muscles. In the biopsy of the hypertrophied gastrocn
Publikováno v:
Musclenerve. 20(2)