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Titolo Data di pubblicazione Autore(i) File
Sensivity and specificity of different electrophysiologic tests in evalutation of lumbosacral radiculopathies 1-gen-1990 Zappia, M.; Bono, F.; Valentino, P.; Puccio, G.; Lavano, A
F-WAVE NORMATIVE studies in different nerves of helthy subjects 1-gen-1993 Zappia, M; Valentino, P; Marchello, Lp; Paniccia, P; Montagna, M
Chronic inflammatory demyelinating polyneuropathy in patient with rheumatoid arthritis 1-gen-1995 Zappia, M; Valentino, P; Bono, F; Vita, G; Aguglia, U; Messina, C; Quattrone, A.
CHRONIC INFIAMMATORY DEMYELINATING POLYNEUROPATHY IN PATIENT WITH RHEUMATOID ARTHRITIS 1-gen-1995 Zappia, M; Valentino, P; Bono, F; Vita, G; Messina, C; Quattrone, A
Negative myoclonus during valproate-related stupor. Neurophysiological evidence of a cortical non-epileptic origin. 1-gen-1995 Aguglia, U; Gambardella, A; Zappia, M; Valentino, P; Quattrone, A.
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths 1-gen-1996 Quattrone, A.; Gambardella, A; Bono, F.; Aguglia, U.; Bolino, A.; Bruni, Ac.; Montesi, Mp.; Oliveri, Rl.; Sabatelli, M.; Tamburrini, O.; Valentino, P.; Van Broeckhoven, C.; Zappia, M.
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family. 1-gen-1996 Quattrone, A; Gambardella, A; Bono, F; Aguglia, U; Bolino, A; Bruni, Ac; Montesi, Mp; Oliveri, Rl; Sabatelli, M; Tamburrini, O; Valentino, P; Van Broeckhoven, C; Zappia, M.
Action palatal tremor in a patient with primary intestinal lymphoma 1-gen-1997 Gambardella, A; Zappia, M.; Valentino, P.; Aguglia, U.; Fera, F.; Pardatscher, K.; A. Quattrone.,
ACTION PALATAL TREMOR IN PATIENT WITH PRIMARY INTESTINAL LYMPHOMA 1-gen-1997 Gambardella, A; Zappia, M; Valentino, P; Aguglia, A; Fera, F; Pardatscher, ; Qattrone, A
Palatal tremor in a patient with primary intestinal lymphoma 1-gen-1997 Gambardella, A; Zappia, M; Valentino, P; Aguglia, U; Fera, F; Pardatscher, K; Quattrone, A
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) 1-gen-1998 Gambardella, A; Bolino, A.; Muglia, M.; Bono, F.; Valentino, P.; Oliveri, Rl.; Sabatelli, M.; Md, ; VAN BROECKHOVEN, C.; Romeo, G.; Devoto, M.; A. QUATTRONE.,
PULSED METHYLPREDNISOLONE INDUCES A REVERSIBLE IMPAIRMENT OF MEMORY IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS 1-gen-1998 Oliveri, Rl; Sibilia, G; Valentino, P; Russo, C; Romeo, N; Quattrone, A
GENETIC HETEROGENEITY IN AUTOSOMAL RECESSIVE HEREDITARY MOTOR AND SENSORY NEUROPHATY WITH FOCALLY FOLDED MYELIN SHEATHS (CMT4B) 1-gen-1998 Gambardella, A; Bolino, A; Muglia, M; Valentino, P; Bono, F; Oliver, Rl; Sabatelli, M; Brancolini, V; VAN BROCKHOVEN, C; Romeo, G; Devot, M; Quattrone, A
Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study 1-gen-1998 Oliveri, Rl; Valentino, P; Russo, C; Sibilia, G; Aguglia, U; Bono, F; Fera, F; Zappia, M; Pardatscher, K; Quattrone, A.; Gambardella, A
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 1-gen-1998 Gambardella, A; Mazzei, R; Toscano, A; Annesi, G; Pasqua, A; Annesi, F; Quattrone, F; Oliveri, Rl; Valentino, P; Bono, F; Aguglia, U; Zappia, M; Vita, G; Quattrone, A.
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 1-gen-1998 Gambardella, A; Mazzei, R; Toscano, A; Annesi, G; Pasqua, A; Annesi, F; Quattrone, F; Oliveri, Rl; Valentino, P; Bono, F; Aguglia, U; Quattrone, A
Kufs’ disease presenting as late-onset epilepsia partialis continua 1-gen-1998 Gambardella, A.; Pasquinelli, G.; Cittadella, R.; Bono, F.; Oliveri, Rl.; Zappia, M.; Aguglia, U; Gambardella, A; Valentino, P
RANDOMIZED TRIAL COMPARING TWO DIFFERENT HIGH DOSES OF METHYLPREDNISOLONE IN MS: A CLINICAL AND MRI SUDY 1-gen-1998 Oliver, Rl; Valentino, P; Russo, C; Sibilia, G; Aguglia, U; Bono, F; Fera, F; Gambardella, A; Zappia, M; Pardatscher, K; Quattrone, A
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity 1-gen-1998 Gambardella, A; Annesi, G; Bono, F; Spadafora, P; Valentino, P; Pasqua, Aa; Mazzei, R; Montesanti, R; Conforti, Fl; Oliveri, Rl; Zappia, M; Aguglia, U; Quattrone, A.
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) 1-gen-1999 Gambardella, A; Bono, F; Muglia, M; Quattrone, A; Valentino, P
Mostrati risultati da 1 a 20 di 155
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