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Cancer
|
October 15, 1994
Hereditary and familial ovarian cancer in southern Ontario
S 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 gene
N 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 myositis
G 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 cases
L 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 dystrophy
G 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 monitoring
F 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 fibers
C 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 myopathy
G Vattemi, P Tonin, M Mora, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 110) with videos related to
Sort By:
Page
of 11
Cancer
|
October 15, 1994
Hereditary and familial ovarian cancer in southern Ontario
S 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 gene
N 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 myositis
G 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 cases
L 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 dystrophy
G 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 monitoring
F 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 fibers
C 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 myopathy
G Vattemi, P Tonin, M Mora, et al.
Page
of 11