Zobrazeno 1 - 10
of 35
pro vyhledávání: '"B. Sferrazza"'
Autor:
Stefano C. Previtali, Angelo Quattrini, B. Sferrazza, C. Casellato, Sandro Iannaccone, Marina Scarlato, Eduardo Nobile-Orazio, Nilo Riva, Massimo Corbo, Giancarlo Comi, A. Lazzerini, Federica Cerri
Publikováno v:
Annals of Neurology. 69:197-201
Early differential diagnosis of motor neuropathies (MN) and lower motor neuron diseases (LMND) is important, as prognosis and therapeutic approaches are different. We evaluated the diagnostic contribution of the biopsy of the motor branch of the obtu
Autor:
Lucia De Monte, Stefano F. Cappa, Stefano Olivieri, Sandro Iannaccone, Massimo Alessio, B. Sferrazza, Antonio Conti, Diego Franciotta
Publikováno v:
PROTEOMICS - CLINICAL APPLICATIONS. 2:1628-1637
Amyotrophic lateral sclerosis (ALS) a fatal degenerative disease that selectively affects motor neurons, likely results from a complex interplay among oxidative injury, excitotoxic stimulation, protein aggregation and genetic factors. Ceruloplasmin (
Autor:
Mauro Manconi, Luigi Ferini-Strambi, B. Sferrazza, Marco Zucconi, Antonio Massimo, Sandro Iannaccone
Publikováno v:
Movement Disorders. 20:1646-1650
Propriospinal myoclonus is a rare motor disorder consisting of involuntary spinal-generated muscular jerks. Here, we report a severe and uncommon case of propriospinal myoclonus that appeared after a vertebral fracture of T11. In this patient, the po
Autor:
B. Sferrazza, V. Golzi, Sandro Iannaccone, F. de Rino, Salvatore Smirne, Luigi Ferini-Strambi
Publikováno v:
Headache: The Journal of Head and Face Pain. 39:666-669
Almost 95 cases of superficial siderosis of the central nervous system have been reported in the literature. These patients showed a clinical syndrome characterized by ataxia, deafness, pyramidal system involvement, and mental deterioration with xant
Autor:
Monica Consonni, Alberto Raggi, Daniela Perani, Stefano F. Cappa, Michele Zamboni, Sandro Iannaccone, B. Sferrazza
Objective To investigate the presence of sub-clinical cognitive dysfunction in non-demented patients with amyotrophic lateral sclerosis (ALS) using auditory event-related potentials (ERPs). Methods Ten subjects with ALS and 10 age- and sex-matched co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::720e07ab65be3ee397326c2dba8dcbb5
Autor:
Raffaello Nemni, Giovanni Ricevuti, Sandro Iannaccone, B. Sferrazza, Angelo Quattrini, A. Lazzerini, Giacomo Dell'Antonio
Publikováno v:
Neurology. 51:600-602
We report a 57-year-old man with progressive symmetric weakness and fasciculation affecting the legs. Electromyography revealed fibrillations and neurogenic motor unit potentials in the leg muscles. Biopsy of a motor branch of the obturator nerve rev
Autor:
Sandro Iannaccone, Massimiliano Beltramo, B. Sferrazza, Antonio Conti, Angela Bachi, Angela Cattaneo, Piero Ricchiuto, Massimo Alessio, Angelo Reggiani
Publikováno v:
Proteomics
Proteomics, Wiley-VCH Verlag, 2005, 5 (17), pp.4558-4567. ⟨10.1002/pmic.200402088⟩
Proteomics, Wiley-VCH Verlag, 2005, 5 (17), pp.4558-4567. ⟨10.1002/pmic.200402088⟩
Peripheral neuropathies are characterized by asymmetrical slowly progressive weakness with no upper motor neuron signs, and can occur either with or without pain. Due to poor knowledge of the disease mechanisms, available pain treatment is very limit
Autor:
Corrado Angelini, D. Toniolo, M. Trisciani, B. Sferrazza, Enrico Bertini, G. Comi, Angelo Quattrini, Paola Carrera, Stefano C. Previtali, Sandro Iannaccone, Sara Benedetti, Maurizio Ferrari
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 76(7)
The coexistence of neurogenic and myogenic features in scapuloperoneal syndrome is rarely ascribed to a single gene. Defects in the nuclear envelope protein lamin A/C, encoded by the LMNA gene, have been shown to be associated with a variety of disor
Publikováno v:
Sleep research online : SRO. 1(1)
Muscular pharyngeal structural changes, as fibre type disproportion, have been described in patients affected by Obstructive Sleep Apnea (OSA) and in an animal experimental OSA model. The unsolved question is whether these muscular abnormalities are
Autor:
S. Iannaccone, A. Quattrini, B. Sferrazza, L. Ferini-Strambi, F. Gemignani, A. Marbini, M. G. Terzano
Publikováno v:
Neurology. 54:1013-1014