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Showing results (131-140 of 346) with videos related to

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Science (New York, N.Y.)|August 5, 2000
Role of adenine nucleotide translocator 1 in mtDNA maintenanceJ Kaukonen, J K Juselius, V Tiranti, et al.
Nucleic Acids Research|May 25, 1988
An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoterR Mantovani, N Malgaretti, S Nicolis, et al.
Blood|December 1, 1980
Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriersB Giglioni, P Comi, R Taramelli, et al.
Journal of Child Neurology|January 8, 2013
Congenital myasthenic syndrome due to choline acetyltransferase mutations in infants: clinical suspicion and comprehensive electrophysiological assessment are important for early diagnosisRobertino Dilena, Angela Abicht, Paola Sergi, et al.
Cell|May 1, 1976
A direct estimate of the number of human gamma-globin genesJ Old, J B Clegg, D J Weatherall, et al.
Blood|March 1, 1988
Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoterS Ottolenghi, S Nicolis, R Taramelli, et al.
Frontiers in Neurology|June 1, 2022
Newly Diagnosed Hepatic Encephalopathy Presenting as Non-convulsive Status Epilepticus: A Case Report and Literature ReviewMarco Olivero, Delia Gagliardi, Gianluca Costamagna, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Pageof 35

Showing results (131-140 of 346) with videos related to

Sort By:
Pageof 35
Science (New York, N.Y.)|August 5, 2000
Role of adenine nucleotide translocator 1 in mtDNA maintenanceJ Kaukonen, J K Juselius, V Tiranti, et al.
Nucleic Acids Research|May 25, 1988
An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoterR Mantovani, N Malgaretti, S Nicolis, et al.
Blood|December 1, 1980
Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriersB Giglioni, P Comi, R Taramelli, et al.
Journal of Child Neurology|January 8, 2013
Congenital myasthenic syndrome due to choline acetyltransferase mutations in infants: clinical suspicion and comprehensive electrophysiological assessment are important for early diagnosisRobertino Dilena, Angela Abicht, Paola Sergi, et al.
Cell|May 1, 1976
A direct estimate of the number of human gamma-globin genesJ Old, J B Clegg, D J Weatherall, et al.
Blood|March 1, 1988
Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoterS Ottolenghi, S Nicolis, R Taramelli, et al.
Frontiers in Neurology|June 1, 2022
Newly Diagnosed Hepatic Encephalopathy Presenting as Non-convulsive Status Epilepticus: A Case Report and Literature ReviewMarco Olivero, Delia Gagliardi, Gianluca Costamagna, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Pageof 35