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R Barresi

Showing results (21-30 of 39) with videos related to

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Neuromuscular Disorders : NMD|June 29, 2010
Calpainopathy presenting as foot drop in a 41 year oldG Burke, C Hillier, J Cole, et al.
Clinical Genetics|July 14, 2016
Muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletionT A Willis, C L Wood, J Hudson, et al.
The Journal of Clinical Investigation|August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokineP Bernasconi, E Torchiana, P Confalonieri, et al.
Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.
Journal of the Neurological Sciences|October 1, 1995
Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotypeL Morandi, M Mora, V Confalonieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2009
Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigreeT D Miller, A P Jackson, R Barresi, et al.
Journal of Medical Genetics|February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutationsR Barresi, C Di Blasi, T Negri, et al.
Transfusion Science|June 1, 2000
PCR testing for HCV in anti-HCV negative blood donors involved in the so called HCV +ve post-transfusion hepatitisM R Ruzzenenti, M C De Luigi, R Bruni, et al.
Neurology|April 2, 2008
A refined diagnostic algorithm for Bethlem myopathyD Hicks, A K Lampe, R Barresi, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrumL Klinge, A F Dean, W Kress, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|June 29, 2010
Calpainopathy presenting as foot drop in a 41 year oldG Burke, C Hillier, J Cole, et al.
Clinical Genetics|July 14, 2016
Muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletionT A Willis, C L Wood, J Hudson, et al.
The Journal of Clinical Investigation|August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokineP Bernasconi, E Torchiana, P Confalonieri, et al.
Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.
Journal of the Neurological Sciences|October 1, 1995
Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotypeL Morandi, M Mora, V Confalonieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2009
Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigreeT D Miller, A P Jackson, R Barresi, et al.
Journal of Medical Genetics|February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutationsR Barresi, C Di Blasi, T Negri, et al.
Transfusion Science|June 1, 2000
PCR testing for HCV in anti-HCV negative blood donors involved in the so called HCV +ve post-transfusion hepatitisM R Ruzzenenti, M C De Luigi, R Bruni, et al.
Neurology|April 2, 2008
A refined diagnostic algorithm for Bethlem myopathyD Hicks, A K Lampe, R Barresi, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrumL Klinge, A F Dean, W Kress, et al.
Pageof 4