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M Moggio

Showing results (51-60 of 121) with videos related to

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Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Brain : a Journal of Neurology|January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cellsP Baron, D Galimberti, L Meda, et al.
Clinical Neuropathology|July 1, 1991
Muscle biopsy in Alzheimer's disease: morphological and biochemical findingsC Mariani, N Bresolin, E Farina, et al.
Neurology|February 13, 2002
Women with pregnancy-related polymyositis and high serum CK levels in the newbornS Messina, G Fagiolari, C Lamperti, et al.
The Pediatric Infectious Disease Journal|October 1, 1995
Over five-year follow-up of Oka/Merck varicella vaccine recipients in 465 infants and adolescentsD A Clements, C B Armstrong, A M Ursano, et al.
Headache|August 1, 1988
Mitochondrial abnormalities in migraine. Preliminary findingsP Montagna, T Sacquegna, P Martinelli, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Clinical Neuropathology|April 10, 2009
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanomaM E Fruguglietti, L Napoli, M Sciacco, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 6, 2013
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patientS Lucchiari, G Ulzi, F Magri, et al.
Pageof 13

Showing results (51-60 of 121) with videos related to

Sort By:
Pageof 13
Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Brain : a Journal of Neurology|January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cellsP Baron, D Galimberti, L Meda, et al.
Clinical Neuropathology|July 1, 1991
Muscle biopsy in Alzheimer's disease: morphological and biochemical findingsC Mariani, N Bresolin, E Farina, et al.
Neurology|February 13, 2002
Women with pregnancy-related polymyositis and high serum CK levels in the newbornS Messina, G Fagiolari, C Lamperti, et al.
The Pediatric Infectious Disease Journal|October 1, 1995
Over five-year follow-up of Oka/Merck varicella vaccine recipients in 465 infants and adolescentsD A Clements, C B Armstrong, A M Ursano, et al.
Headache|August 1, 1988
Mitochondrial abnormalities in migraine. Preliminary findingsP Montagna, T Sacquegna, P Martinelli, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Clinical Neuropathology|April 10, 2009
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanomaM E Fruguglietti, L Napoli, M Sciacco, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 6, 2013
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patientS Lucchiari, G Ulzi, F Magri, et al.
Pageof 13