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P Sabatelli

Showing results (31-40 of 56) with videos related to

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Histochemistry|September 1, 1992
A combined ultrastructural approach to the study of nuclear matrix thermal stabilizationE Falcieri, P Gobbi, P Sabatelli, et al.
Acta Neuropathologica|February 9, 2000
Hepatitis C virus infection and myositis: a polymerase chain reaction studyM Villanova, C Caudai, P Sabatelli, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjectsS Squarzoni, M Villanova, P Sabatelli, et al.
Muscle & Nerve|July 9, 1999
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophyA Ognibene, P Sabatelli, S Petrini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2001
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VIO Camacho Vanegas, E Bertini, R Z Zhang, et al.
Free Radical Biology & Medicine|July 15, 2014
Monoamine oxidase inhibition prevents mitochondrial dysfunction and apoptosis in myoblasts from patients with collagen VI myopathiesE Sorato, S Menazza, A Zulian, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Minerva Anestesiologica|July 1, 1997
[Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine]S Faenza, R Fato, S Lari, et al.
Neuropathology and Applied Neurobiology|January 28, 2010
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' musclesR Massa, M B Panico, S Caldarola, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Histochemistry|September 1, 1992
A combined ultrastructural approach to the study of nuclear matrix thermal stabilizationE Falcieri, P Gobbi, P Sabatelli, et al.
Acta Neuropathologica|February 9, 2000
Hepatitis C virus infection and myositis: a polymerase chain reaction studyM Villanova, C Caudai, P Sabatelli, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjectsS Squarzoni, M Villanova, P Sabatelli, et al.
Muscle & Nerve|July 9, 1999
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophyA Ognibene, P Sabatelli, S Petrini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2001
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VIO Camacho Vanegas, E Bertini, R Z Zhang, et al.
Free Radical Biology & Medicine|July 15, 2014
Monoamine oxidase inhibition prevents mitochondrial dysfunction and apoptosis in myoblasts from patients with collagen VI myopathiesE Sorato, S Menazza, A Zulian, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Minerva Anestesiologica|July 1, 1997
[Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine]S Faenza, R Fato, S Lari, et al.
Neuropathology and Applied Neurobiology|January 28, 2010
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' musclesR Massa, M B Panico, S Caldarola, et al.
Pageof 6