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G Guazzi

Showing results (21-30 of 28) with videos related to

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Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndromeG M Fabrizi, E Cardaioli, G S Grieco, et al.
Journal of the Neurological Sciences|June 1, 1994
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a familyA Malandrini, G M Fabrizi, F Truschi, et al.
The Journal of Rheumatology|May 17, 2000
Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 casesA Malandrini, E Selvi, M Villanova, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
La Radiologia Medica|October 1, 1996
[Interstitial photocoagulation with laser in the treatment of liver metastasis]C M Pacella, G Bizzarri, F S Ferrari, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndromeG M Fabrizi, E Cardaioli, G S Grieco, et al.
Journal of the Neurological Sciences|June 1, 1994
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a familyA Malandrini, G M Fabrizi, F Truschi, et al.
The Journal of Rheumatology|May 17, 2000
Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 casesA Malandrini, E Selvi, M Villanova, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
La Radiologia Medica|October 1, 1996
[Interstitial photocoagulation with laser in the treatment of liver metastasis]C M Pacella, G Bizzarri, F S Ferrari, et al.
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