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L Morandi

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European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|August 23, 2016
The impact of field cancerization on the extent of duct carcinoma in situ (DCIS) in breast tissue after conservative excisionS Asioli, L Morandi, C Cavatorta, et al.
Experimental Cell Research|August 20, 2011
Fibroblasts from the muscles of Duchenne muscular dystrophy patients are resistant to cell detachment apoptosisS Zanotti, S Gibertini, C Bragato, et al.
Revue Neurologique|January 1, 1986
[Acute myopathy and hyperthyroidism]E Bottacchi, F Cornelio, M Camerlingo, et al.
Virchows Archiv : an International Journal of Pathology|January 15, 2002
TT virus-related acute recurrent hepatitis. Histological features of a case and review of the literatureM P Foschini, L Morandi, S Macchia, et al.
Giornale Italiano Di Cardiologia|September 1, 1988
Dilated cardiomyopathy and successful cardiac transplantation in Becker's muscular distrophy. Follow-up after two yearsF Casazza, G Brambilla, A Salvato, et al.
Journal of Neurology|June 9, 1998
A new non-radioactive method for the screening and prenatal diagnosis of myotonic dystrophy patientsR Brugnoni, L Morandi, B Brambati, et al.
Journal of Neurology|July 1, 1989
Neurogenic muscle hypertrophy. Report of two casesD Pareyson, L Morandi, V Scaioli, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 12, 2010
Low bone density and bone metabolism alterations in Duchenne muscular dystrophy: response to calcium and vitamin D treatmentM L Bianchi, L Morandi, E Andreucci, et al.
Acta Neuropathologica|October 1, 1996
Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriersC Di Blasi, L Morandi, R Barresi, et al.
Brain : a Journal of Neurology|April 5, 2001
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingC Di Blasi, Y He, L Morandi, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|August 23, 2016
The impact of field cancerization on the extent of duct carcinoma in situ (DCIS) in breast tissue after conservative excisionS Asioli, L Morandi, C Cavatorta, et al.
Experimental Cell Research|August 20, 2011
Fibroblasts from the muscles of Duchenne muscular dystrophy patients are resistant to cell detachment apoptosisS Zanotti, S Gibertini, C Bragato, et al.
Revue Neurologique|January 1, 1986
[Acute myopathy and hyperthyroidism]E Bottacchi, F Cornelio, M Camerlingo, et al.
Virchows Archiv : an International Journal of Pathology|January 15, 2002
TT virus-related acute recurrent hepatitis. Histological features of a case and review of the literatureM P Foschini, L Morandi, S Macchia, et al.
Giornale Italiano Di Cardiologia|September 1, 1988
Dilated cardiomyopathy and successful cardiac transplantation in Becker's muscular distrophy. Follow-up after two yearsF Casazza, G Brambilla, A Salvato, et al.
Journal of Neurology|June 9, 1998
A new non-radioactive method for the screening and prenatal diagnosis of myotonic dystrophy patientsR Brugnoni, L Morandi, B Brambati, et al.
Journal of Neurology|July 1, 1989
Neurogenic muscle hypertrophy. Report of two casesD Pareyson, L Morandi, V Scaioli, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 12, 2010
Low bone density and bone metabolism alterations in Duchenne muscular dystrophy: response to calcium and vitamin D treatmentM L Bianchi, L Morandi, E Andreucci, et al.
Acta Neuropathologica|October 1, 1996
Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriersC Di Blasi, L Morandi, R Barresi, et al.
Brain : a Journal of Neurology|April 5, 2001
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingC Di Blasi, Y He, L Morandi, et al.
Pageof 11