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P Tonin

Showing results (21-30 of 110) with videos related to

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Neuromuscular Disorders : NMD|June 19, 2001
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagiaM Spagnolo, G Tomelleri, G Vattemi, et al.
Electromyography and Clinical Neurophysiology|February 20, 2002
Masked myoclonus in corticobasal degeneration: neurophysiological study of a caseF Piccione, F Meneghello, K Priftis, et al.
American Journal of Human Genetics|May 1, 1994
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiencyS Tsujino, S Servidei, P Tonin, et al.
Neuropathology and Applied Neurobiology|February 13, 2003
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseasesM Filosto, P Tonin, G Vattemi, et al.
Lancet (London, England)|January 22, 1994
Histology of BRCA1-associated ovarian tumoursS Narod, P Tonin, H Lynch, et al.
Minerva Pediatrica|March 1, 1991
[Myopathy with lipid accumulation and type-II glutaric aciduria]G Tomelleri, A Burlina, L Deotto, et al.
Journal of Neuroimmunology|November 7, 2000
T-cell anti-apoptotic mechanisms in inflammatory myopathiesG Vattemi, P Tonin, M Filosto, et al.
Neurology|September 25, 2003
Reversible upper limb muscle weakness with selective loss of thick filamentsG Vattemi, P Tonin, M Filosto, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotypeB Garavaglia, V Colamaria, F Carrara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 4, 2001
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case reportM Filosto, P Tonin, G Vattemi, et al.
Pageof 11

Showing results (21-30 of 110) with videos related to

Sort By:
Pageof 11
Neuromuscular Disorders : NMD|June 19, 2001
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagiaM Spagnolo, G Tomelleri, G Vattemi, et al.
Electromyography and Clinical Neurophysiology|February 20, 2002
Masked myoclonus in corticobasal degeneration: neurophysiological study of a caseF Piccione, F Meneghello, K Priftis, et al.
American Journal of Human Genetics|May 1, 1994
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiencyS Tsujino, S Servidei, P Tonin, et al.
Neuropathology and Applied Neurobiology|February 13, 2003
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseasesM Filosto, P Tonin, G Vattemi, et al.
Lancet (London, England)|January 22, 1994
Histology of BRCA1-associated ovarian tumoursS Narod, P Tonin, H Lynch, et al.
Minerva Pediatrica|March 1, 1991
[Myopathy with lipid accumulation and type-II glutaric aciduria]G Tomelleri, A Burlina, L Deotto, et al.
Journal of Neuroimmunology|November 7, 2000
T-cell anti-apoptotic mechanisms in inflammatory myopathiesG Vattemi, P Tonin, M Filosto, et al.
Neurology|September 25, 2003
Reversible upper limb muscle weakness with selective loss of thick filamentsG Vattemi, P Tonin, M Filosto, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotypeB Garavaglia, V Colamaria, F Carrara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 4, 2001
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case reportM Filosto, P Tonin, G Vattemi, et al.
Pageof 11