Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alex Papadimitriou"'
Autor:
Georgios M. Hadjigeorgiou, Evangelia E. Tsironi, Efthimios H Mikropoulos, Afroditi A. Papathanasiou, Alex Papadimitriou
Publikováno v:
The Open Neurology Journal. 4:92-99
Introduction: The Blink Reflex Test (BRT) is a neurophysiological examination used for evaluation of brain- stem reflex circuits. MRI is the most precise modality for evaluation of MS lesion anatomy. Our study objective was to investigate how the fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66eb0be4e6dd1f49dfe91d75b70009be
https://doi.org/10.2174/1874205x01004010092
https://doi.org/10.2174/1874205x01004010092
Publikováno v:
Annals of Neurology. 41:25-31
We describe 2 Greek siblings who developed a rapidly progressive oculopharyngeal somatic syndrome, at the ages of 11 and 14 years, with muscle biopsies showing rimmed vacuoles and, in 1 case, cytoplasmic and intranuclear tubulofilamentous inclusions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::351b29ac37f0a2e1df236f1276dab566
https://doi.org/10.1002/ana.410410107
https://doi.org/10.1002/ana.410410107
Autor:
Efthimios H, Mikropoulos, Afroditi A, Papathanasiou, Georgios, Hadjigeorgiou, Evangelia, Tsironi, Alex, Papadimitriou
Publikováno v:
The Open Neurology Journal
Introduction The Blink Reflex Test (BRT) is a neurophysiological examination used for evaluation of brainstem reflex circuits. MRI is the most precise modality for evaluation of MS lesion anatomy. Our study objective was to investigate how the functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d457ec628328194a0334a88a337dba29
https://pubmed.ncbi.nlm.nih.gov/21347209
https://pubmed.ncbi.nlm.nih.gov/21347209
Autor:
Maria Bonsignore, Monica Sciacco, Andrea Martinuzzi, Antonio Toscano, Alessandro Prelle, Alex Papadimitriou, Marco Crimi, Giacomo P. Comi, Carmelo Rodolico, Anastasia Garufi, Sara Galbiati, Andreina Bordoni, Dimitra Papadimitriou, Efi Katsarou, M.’hammed Aguennouz, Nereo Bresolin
Publikováno v:
Pediatric neurology. 34(3)
Mitochondrial deoxyribonucleic acid depletion syndromes are autosomal recessive disorders characterized by a reduction of the amount of mitochondrial deoxyribonucleic acid, which impairs the synthesis of respiratory chain complexes. Mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e3c2d618b95e76df855c204dd14dea6
https://pubmed.ncbi.nlm.nih.gov/16504786
https://pubmed.ncbi.nlm.nih.gov/16504786
Autor:
Alex Agathonikou, Sybille Ried, Matthias J. Koepp, Chrysostomos P. Panayiotopoulos, Alex Papadimitriou, Gordon T. Plant, Michael Koutroumanidis, Mark P. Richardson, Carol Camfield, John S. Duncan
Publikováno v:
Brain : a journal of neurology. 121
We present the clinical and electrographic data of 17 patients with reading-induced seizures documented with ictal video-EEG studies during provocation with language related tasks. The median age at onset was 15 years (range 11-22 years) and the male
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a53806c3c6335ad8d1a402816db7b952
https://pubmed.ncbi.nlm.nih.gov/9712004
https://pubmed.ncbi.nlm.nih.gov/9712004
Autor:
Guglielmo Scarlato, Andreina Bordoni, Nicoletta Checcarelli, Giacomo P. Comi, Maurizio Moggio, Alex Papadimitriou, Allessandro Prelle, Nereo Bresolin, Gigliola Fagiolari
Publikováno v:
Journal of the neurological sciences. 123(1-2)
Multiple deletions of mitochondrial DNA (mtDNA) were first identified in patients with mitochondrial encephalomyopathy with a clear mendelian inheritance. We found this genetic alteration in four atypical and sporadic cases of mitochondrial encephalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd9b88bda40dcce8f1ebe9f55123e75f
https://pubmed.ncbi.nlm.nih.gov/8064325
https://pubmed.ncbi.nlm.nih.gov/8064325
Autor:
Gigliola Fagiolari, Francesco Fortunato, Giacomo P. Comi, Lucia Tancredi, Maurizio Moggio, Costanza Lamperti, L. Adobbati, Patrizia Ciscato, Alessandro Prelle, L. Napoli, Nereo Bresolin, Monica Sciacco, Antonio Toscano, Alessandro Battistel, Luca Chiveri, Stefano Messina, Filippo Martinelli-Boneschi, Maria Paola Perini, Alex Papadimitriou, Guglielmo Scarlato, Andreina Bordoni
Publikováno v:
Scopus-Elsevier
Mitochondrial disorders are human genetic diseases with extremely variable clinical and genetic features. To better define them, we made a genotype-phenotype correlation in a series of 207 affected patients, and we examined most of them with six labo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22528683cb5a57151f431d2e30649f4e
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034870693&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034870693&partnerID=MN8TOARS
