Zobrazeno 1 - 10
of 12
pro vyhledávání: '"G P, Comi"'
Autor:
V. Montano, P. Lopriore, F. Gruosso, V. Carelli, G. P. Comi, M. Filosto, C. Lamperti, T. Mongini, O. Musumeci, S. Servidei, P. Tonin, A. Toscano, G. Primiano, M. L. Valentino, S. Bortolani, S. Marchet, G. Ricci, A. Modenese, S. Cotti Piccinelli, B. Risi, M. Meneri, I. G. Arena, G. Siciliano, Michelangelo Mancuso
Objectives To assess natural history and 12-month change of a series of scales and functional outcome measures in a cohort of 117 patients with primary mitochondrial myopathy (PMM). Methods Twelve months follow-up data of 117 patients with PMM were c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9129bcd1fff4ec5dec18846855237465
https://hdl.handle.net/11379/564661
https://hdl.handle.net/11379/564661
Autor:
J. Abutalebi, C. Arcari, M. A. Rocca, P. Rossi, M. Comola, G. C. Comi, M. Rovaris, M. Filippi
Publikováno v:
Behavioural Neurology, Vol 18, Iss 3, Pp 183-186 (2007)
Externí odkaz:
https://doaj.org/article/f20f85f4e6554ebca25ba5d1e1dd97a4
Autor:
L. Tancredi, F. Martinelli Boneschi, M. Braga, I. Santilli, C. Scaccabarozzi, P. Lattuada, M. Sessa, L. Fumagalli, S. Iurlaro, I. Neromante, M. L. De Lodovici, D. V. Roccatagliata, G. Giacalone, M. Arnaboldi, V. Crespi, E. Agostoni, G. C. Comi, C. Ferrarese, R. Sterzi
Publikováno v:
Stroke Research and Treatment, Vol 2013 (2013)
The aims of this study were (i) to evaluate the clinical features of a consecutive series of young patients with ischemic stroke and (ii) to assess the changes in the clinical management of these patients over the study period. All consecutive cases
Externí odkaz:
https://doaj.org/article/6df73bb01c7d4828ba252e225c8b3249
Autor:
Y. Torrente, M. Belicchi, C. Marchesi, G. D'antona, F. Cogiamanian, F. Pisati, M. Gavina, R. Giordano, R. Tonlorenzi, G. Fagiolari, C. Lamperti, L. Porretti, R. Lopa, M. Sampaolesi, L. Vicentini, N. Grimoldi, F. Tiberio, V. Songa, P. Baratta, A. Prelle, L. Forzenigo, M. Guglieri, O. Pansarasa, C. Rinaldi, V. Mouly, G. S. Butler-Browne, G. P. Comi, P. Biondetti, M. Moggio, S. M. Gaini, N. Stocchetti, A. Priori, M. G. D'angelo, A. Turconi, R. Bottinelli, G. Cossu, P. Rebulla, N. Bresolin
Publikováno v:
Cell Transplantation, Vol 16 (2007)
Duchenne muscular dystrophy (DMD) is a lethal X-linked recessive muscle disease due to defect on the gene encoding dystrophin. The lack of a functional dystrophin in muscles results in the fragility of the muscle fiber membrane with progressive muscl
Externí odkaz:
https://doaj.org/article/1c17f98f55584c398b44b1829742f0d3
Autor:
Y. Torrente, M. G. D'angelo, R. Del Bo, A. Deliso, R. Casati, R. Benti, S. Corti, G. P. Comi, P. Gerundini, A. Anichini, G. Scarlato, N. Bresolin
Publikováno v:
Cell Transplantation, Vol 8 (1999)
The deficiency of dystrophin, a sarcolemmal associated protein, is responsible for Duchenne muscular dystrophy (DMD). Gene replacement is attractive as a potential therapy. In this article, we describe a new method for myoblast transplantation and ex
Externí odkaz:
https://doaj.org/article/15ad3d922f4c4f4f9bdff16903d83f83
Autor:
Amira, Mili, Ilhem, Ben Charfeddine, Ons, Mamaï, Sonia, Abdelhak, Labiba, Adala, Abdelbasset, Amara, Serena, Pagliarani, Sabrina, Lucchiarri, Sabrina, Lucchiari, Abdelkarim, Ayadi, Neji, Tebib, Abdelaziz, Harbi, Jihene, Bouguila, Dorra, H'Mida, Ali, Saad, Khalifa, Limem, G P, Comi, Moez, Gribaa
Publikováno v:
Journal of human genetics. 57(3)
Glycogen storage disease type III (GSD III) is an autosomal recessive inborn error of metabolism caused by mutations in the glycogen debranching enzyme amylo-1,6-glucosidase gene, which is located on chromosome 1p21.2. GSD III is characterized by the
Publikováno v:
Histology and histopathology. 20(3)
Cell-based therapy may represent a new strategy to treat a vast array of clinical disorders including neurodegenerative diseases. Recent observations indicate that adult somatic stem cells have the capacity to contribute to the regeneration of differ
Autor:
A, Prelle, M, Sciacco, G P, Comi, S, Messina, M, Carpo, P, Ciscato, E, Nobile Orazio, F, Fortunato, G, Mora, V, Bignotti, G, Fagiolari, M, Moggio, G, Scarlato
Publikováno v:
Clinical neuropathology. 19(4)
Recently, abnormal expression of cyclin-dependent kinases was proposed as a possible cause of desminopathy. We describe an atypical case clinically characterized by severe respiratory distress. Muscle biopsy showed subsarcolemmal and intracytoplasmic
Autor:
Y. Torrente, M. Belicchi, C. Marchesi, G. D'antona, F. Cogiamanian, F. Pisati, M. Gavina, R. Giordano, R. Tonlorenzi, G. Fagiolari, C. Lamperti, L. Porretti, R. Lopa, M. Sampaolesi, L. Vicentini, N. Grimoldi, F. Tiberio, V. Songa, P. Baratta, A. Prelle, L. Forzenigo, M. Guglieri, O. Pansarasa, C. Rinaldi, V. Mouly, G. S. Butler-Browne, G. P. Comi, P. Biondetti, M. Moggio, S. M. Gaini, N. Stocchetti, A. Priori, M. G. D'angelo, A. Turconi, R. Bottinelli, G. Cossu, P. Rebulla, N. Bresolin
Publikováno v:
ResearcherID
Europe PubMed Central
Scopus-Elsevier
Cell Transplantation, Vol 16 (2007)
Europe PubMed Central
Scopus-Elsevier
Cell Transplantation, Vol 16 (2007)
Duchenne muscular dystrophy (DMD) is a lethal X-linked recessive muscle disease due to defect on the gene encoding dystrophin. The lack of a functional dystrophin in muscles results in the fragility of the muscle fiber membrane with progressive muscl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f5f5ac1a366bb0974a29b037ce1c9ed
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000249513200001&KeyUID=WOS:000249513200001
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000249513200001&KeyUID=WOS:000249513200001
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