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A Simonati

Showing results (31-40 of 48) with videos related to

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Neurology|September 17, 1999
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22G M Fabrizi, T Cavallaro, F Taioli, et al.
Acta Neuropathologica|August 12, 2003
MELAS: clinical phenotype and morphological brain abnormalitiesM Sparaco, A Simonati, T Cavallaro, et al.
Acta Neuropathologica|August 31, 2000
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zeroG M Fabrizi, F Taioli, T Cavallaro, et al.
Annals of Neurology|February 1, 1997
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological studyL Bertolasi, A Priori, G Tomelleri, et al.
Neuropediatrics|November 9, 2000
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCLA Simonati, E Santorum, A Tessa, et al.
Journal of Medical Genetics|June 19, 2002
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1M Zortea, A Vettori, C P Trevisan, et al.
Rheumatology (Oxford, England)|July 10, 2008
Sarcoidosis and inclusion body myositisG Vattemi, P Tonin, M Marini, et al.
Muscle & Nerve|June 17, 1998
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty casesG M Fabrizi, A Simonati, M Morbin, et al.
Neuropediatrics|May 1, 1988
Cerebro-ocular dysplasia and muscular dystrophy: report of two casesA Federico, M T Dotti, A Malandrini, et al.
Neurobiology of Disease|November 12, 2023
Integrative human and murine multi-omics: Highlighting shared biomarkers in the neuronal ceroid lipofuscinosesN Gammaldi, F Pezzini, E Michelucci, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Neurology|September 17, 1999
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22G M Fabrizi, T Cavallaro, F Taioli, et al.
Acta Neuropathologica|August 12, 2003
MELAS: clinical phenotype and morphological brain abnormalitiesM Sparaco, A Simonati, T Cavallaro, et al.
Acta Neuropathologica|August 31, 2000
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zeroG M Fabrizi, F Taioli, T Cavallaro, et al.
Annals of Neurology|February 1, 1997
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological studyL Bertolasi, A Priori, G Tomelleri, et al.
Neuropediatrics|November 9, 2000
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCLA Simonati, E Santorum, A Tessa, et al.
Journal of Medical Genetics|June 19, 2002
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1M Zortea, A Vettori, C P Trevisan, et al.
Rheumatology (Oxford, England)|July 10, 2008
Sarcoidosis and inclusion body myositisG Vattemi, P Tonin, M Marini, et al.
Muscle & Nerve|June 17, 1998
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty casesG M Fabrizi, A Simonati, M Morbin, et al.
Neuropediatrics|May 1, 1988
Cerebro-ocular dysplasia and muscular dystrophy: report of two casesA Federico, M T Dotti, A Malandrini, et al.
Neurobiology of Disease|November 12, 2023
Integrative human and murine multi-omics: Highlighting shared biomarkers in the neuronal ceroid lipofuscinosesN Gammaldi, F Pezzini, E Michelucci, et al.
Pageof 5