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P Tonin

Showing results (51-60 of 110) with videos related to

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Cancer|October 15, 1994
Hereditary and familial ovarian cancer in southern OntarioS A Narod, L Madlensky, L Bradley, et al.
Oncogene|June 26, 1997
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor geneN Rahman, L Arbour, P Tonin, et al.
Neurology|February 1, 1993
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)P Tonin, S Shanske, A F Miranda, et al.
Annals of Neurology|March 1, 1994
A splice junction mutation in a new myopathic variant of phosphoglycerate kinase deficiency (PGK North Carolina)S Tsujino, P Tonin, S Shanske, et al.
Rheumatology (Oxford, England)|July 10, 2008
Sarcoidosis and inclusion body myositisG Vattemi, P Tonin, M Marini, et al.
European Neurology|January 1, 1985
Effects of GM1 ganglioside in cerebrovascular diseases: a double-blind trial in 40 casesL Battistin, A Cesari, F Galligioni, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophyG Piccolo, G Azan, P Tonin, et al.
Brain Injury|July 24, 2019
What impact can hospitalization environment produce on the ANS functioning in patients with Unresponsive Wakefulness Syndrome? - 24-hour monitoringF Riganello, G Napoletano, M D Cortese, et al.
Neuromuscular Disorders : NMD|January 1, 1991
An adult-onset myopathy characterized by a double ring appearance of muscle fibersC L Coulter, W A Marks, J B Bodensteiner, et al.
Neurology|May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathyG Vattemi, P Tonin, M Mora, et al.
Pageof 11

Showing results (51-60 of 110) with videos related to

Sort By:
Pageof 11
Cancer|October 15, 1994
Hereditary and familial ovarian cancer in southern OntarioS A Narod, L Madlensky, L Bradley, et al.
Oncogene|June 26, 1997
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor geneN Rahman, L Arbour, P Tonin, et al.
Neurology|February 1, 1993
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)P Tonin, S Shanske, A F Miranda, et al.
Annals of Neurology|March 1, 1994
A splice junction mutation in a new myopathic variant of phosphoglycerate kinase deficiency (PGK North Carolina)S Tsujino, P Tonin, S Shanske, et al.
Rheumatology (Oxford, England)|July 10, 2008
Sarcoidosis and inclusion body myositisG Vattemi, P Tonin, M Marini, et al.
European Neurology|January 1, 1985
Effects of GM1 ganglioside in cerebrovascular diseases: a double-blind trial in 40 casesL Battistin, A Cesari, F Galligioni, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophyG Piccolo, G Azan, P Tonin, et al.
Brain Injury|July 24, 2019
What impact can hospitalization environment produce on the ANS functioning in patients with Unresponsive Wakefulness Syndrome? - 24-hour monitoringF Riganello, G Napoletano, M D Cortese, et al.
Neuromuscular Disorders : NMD|January 1, 1991
An adult-onset myopathy characterized by a double ring appearance of muscle fibersC L Coulter, W A Marks, J B Bodensteiner, et al.
Neurology|May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathyG Vattemi, P Tonin, M Mora, et al.
Pageof 11