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pro vyhledávání: '"G, Amoiridis"'
Akademický článek
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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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::facc3d8e3dc97d20caa9f4d21f4b0e8a
https://doi.org/10.1093/brain/120.12.2131
https://doi.org/10.1093/brain/120.12.2131
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cbb16c4763e2a30651a4587526c7353
https://doi.org/10.1055/s-2007-996312
https://doi.org/10.1055/s-2007-996312
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e87b09d212ad8f8d9d653d33051c28eb
https://pubmed.ncbi.nlm.nih.gov/22632054
https://pubmed.ncbi.nlm.nih.gov/22632054
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7823489dd6a03b49c522614d737e072
https://doi.org/10.1111/j.1755-3768.2010.4335.x
https://doi.org/10.1111/j.1755-3768.2010.4335.x
Akademický článek
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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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7ab415b7d41eb695f6f711639ca4471
https://doi.org/10.1055/s-2008-1060773
https://doi.org/10.1055/s-2008-1060773
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b851b6ae0ffe156c56f719b83800fb1
https://pubmed.ncbi.nlm.nih.gov/9403486
https://pubmed.ncbi.nlm.nih.gov/9403486
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d3aec9f42de4aba3ce4b7d976f38ec4
https://pubmed.ncbi.nlm.nih.gov/9298339
https://pubmed.ncbi.nlm.nih.gov/9298339
Publikováno v:
Musclenerve. 20(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db64a1f2e7ce768daa88d845346de05e
https://pubmed.ncbi.nlm.nih.gov/9040663
https://pubmed.ncbi.nlm.nih.gov/9040663