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M Fanin

Showing results (21-30 of 68) with videos related to

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Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.
Neuropathology and Applied Neurobiology|November 8, 2019
Review: Danon disease: Review of natural history and recent advancesG Cenacchi, V Papa, V Pegoraro, et al.
Neurology|May 1, 1990
Enormous dystrophin in a patient with Becker muscular dystrophyC Angelini, A H Beggs, E P Hoffman, et al.
Muscle & Nerve|October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical courseM Fanin, G A Danieli, M Cadaldini, et al.
The New England Journal of Medicine|February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathyD J Duggan, J R Gorospe, M Fanin, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypesC Angelini, M Fanin, E Pegoraro, et al.
Journal of Child Neurology|January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boyL Salviati, A M Laverda, L Zancan, et al.
Cancer Chemotherapy and Pharmacology|January 4, 2001
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agentsD M Bonifati, C Ori, C R Rossi, et al.
Muscle & Nerve|September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?M Fanin, M P Freda, L Vitiello, et al.
Virchows Archiv : an International Journal of Pathology|August 1, 2019
Update on polyglucosan storage diseasesGiovanna Cenacchi, V Papa, R Costa, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.
Neuropathology and Applied Neurobiology|November 8, 2019
Review: Danon disease: Review of natural history and recent advancesG Cenacchi, V Papa, V Pegoraro, et al.
Neurology|May 1, 1990
Enormous dystrophin in a patient with Becker muscular dystrophyC Angelini, A H Beggs, E P Hoffman, et al.
Muscle & Nerve|October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical courseM Fanin, G A Danieli, M Cadaldini, et al.
The New England Journal of Medicine|February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathyD J Duggan, J R Gorospe, M Fanin, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypesC Angelini, M Fanin, E Pegoraro, et al.
Journal of Child Neurology|January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boyL Salviati, A M Laverda, L Zancan, et al.
Cancer Chemotherapy and Pharmacology|January 4, 2001
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agentsD M Bonifati, C Ori, C R Rossi, et al.
Muscle & Nerve|September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?M Fanin, M P Freda, L Vitiello, et al.
Virchows Archiv : an International Journal of Pathology|August 1, 2019
Update on polyglucosan storage diseasesGiovanna Cenacchi, V Papa, R Costa, et al.
Pageof 7