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A Ferlini

Showing results (21-30 of 88) with videos related to

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American Journal of Human Genetics|July 31, 1998
A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathyA Ferlini, N Galié, L Merlini, et al.
Electrophoresis|May 1, 1994
Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: the case of Kennedy's diseaseM Nesi, P G Righetti, M C Patrosso, et al.
Electroencephalography and Clinical Neurophysiology|October 1, 1996
Electromyographic findings in transthyretin (TTR)-related familial amyloid polyneuropathy (FAP)P Montagna, L Marchello, R Plasmati, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcriptsA M Barbieri, N Soriani, A Ferlini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosisA Ferlini, S Fini, F Salvi, et al.
Human Mutation|July 5, 2001
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTRG Feriotto, A Ferlini, A Ravani, et al.
BMC Cardiovascular Disorders|May 4, 2019
Predictors of cardiac arrhythmic events in non coronary artery disease patientsC Balla, F Vitali, A Brieda, et al.
Advances in Neurology|January 1, 1988
Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studiesA Ferlini, G Romeo, C A Tassinari, et al.
American Journal of Medical Genetics|May 30, 1998
Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosisM C Patrosso, F Salvi, D De Grandis, et al.
Neuropathology and Applied Neurobiology|June 4, 2009
Calpain 3 deficiency presenting as fibre type disproportionG Vattemi, P Tonin, M Neri, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|July 31, 1998
A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathyA Ferlini, N Galié, L Merlini, et al.
Electrophoresis|May 1, 1994
Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: the case of Kennedy's diseaseM Nesi, P G Righetti, M C Patrosso, et al.
Electroencephalography and Clinical Neurophysiology|October 1, 1996
Electromyographic findings in transthyretin (TTR)-related familial amyloid polyneuropathy (FAP)P Montagna, L Marchello, R Plasmati, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcriptsA M Barbieri, N Soriani, A Ferlini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosisA Ferlini, S Fini, F Salvi, et al.
Human Mutation|July 5, 2001
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTRG Feriotto, A Ferlini, A Ravani, et al.
BMC Cardiovascular Disorders|May 4, 2019
Predictors of cardiac arrhythmic events in non coronary artery disease patientsC Balla, F Vitali, A Brieda, et al.
Advances in Neurology|January 1, 1988
Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studiesA Ferlini, G Romeo, C A Tassinari, et al.
American Journal of Medical Genetics|May 30, 1998
Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosisM C Patrosso, F Salvi, D De Grandis, et al.
Neuropathology and Applied Neurobiology|June 4, 2009
Calpain 3 deficiency presenting as fibre type disproportionG Vattemi, P Tonin, M Neri, et al.
Pageof 9