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F Cardone

Showing results (11-20 of 27) with videos related to

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Springerplus|September 22, 2016
The molecular characterization by SSRs reveals a new South Italian kinship and the origin of the cultivar Uva di TroiaC Bergamini, R Perniola, M F Cardone, et al.
Clinical Neuropathology|May 1, 1996
A panencephalopathic type of Creutzfeldt-Jakob disease with selective lesions of the thalamic nuclei in 2 Swiss patientsA Carota, G P Pizzolato, P Gailloud, et al.
Intervirology|January 1, 1997
Highly infectious purified preparations of disease-specific amyloid of transmissible spongiform encephalopathies are not devoid of nucleic acids of viral sizeH Diringer, M Beekes, M Ozel, et al.
Neurology|January 10, 2002
Increased CSF levels of prostaglandin E(2) in variant Creutzfeldt-Jakob diseaseL Minghetti, F Cardone, A Greco, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 1, 1989
Influence of lactate on isoproterenol-induced lipolysis and beta-adrenoceptors distribution in human fat cellsG De Pergola, M Cignarelli, G Nardelli, et al.
Neurology|March 9, 2005
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein geneS Capellari, F Cardone, S Notari, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 23, 2008
Primate chromosome evolution: ancestral karyotypes, marker order and neocentromeresR Stanyon, M Rocchi, O Capozzi, et al.
European Journal of Histochemistry : EJH|June 23, 2004
Localization of beta-defensin genes in non human primatesM Ventura, M Boniotto, M Pazienza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob diseaseM Salvatore, M Pocchiari, F Cardone, et al.
Brain Research Bulletin|September 14, 1999
Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patientsF Cardone, Q G Liu, R Petraroli, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Springerplus|September 22, 2016
The molecular characterization by SSRs reveals a new South Italian kinship and the origin of the cultivar Uva di TroiaC Bergamini, R Perniola, M F Cardone, et al.
Clinical Neuropathology|May 1, 1996
A panencephalopathic type of Creutzfeldt-Jakob disease with selective lesions of the thalamic nuclei in 2 Swiss patientsA Carota, G P Pizzolato, P Gailloud, et al.
Intervirology|January 1, 1997
Highly infectious purified preparations of disease-specific amyloid of transmissible spongiform encephalopathies are not devoid of nucleic acids of viral sizeH Diringer, M Beekes, M Ozel, et al.
Neurology|January 10, 2002
Increased CSF levels of prostaglandin E(2) in variant Creutzfeldt-Jakob diseaseL Minghetti, F Cardone, A Greco, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 1, 1989
Influence of lactate on isoproterenol-induced lipolysis and beta-adrenoceptors distribution in human fat cellsG De Pergola, M Cignarelli, G Nardelli, et al.
Neurology|March 9, 2005
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein geneS Capellari, F Cardone, S Notari, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 23, 2008
Primate chromosome evolution: ancestral karyotypes, marker order and neocentromeresR Stanyon, M Rocchi, O Capozzi, et al.
European Journal of Histochemistry : EJH|June 23, 2004
Localization of beta-defensin genes in non human primatesM Ventura, M Boniotto, M Pazienza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob diseaseM Salvatore, M Pocchiari, F Cardone, et al.
Brain Research Bulletin|September 14, 1999
Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patientsF Cardone, Q G Liu, R Petraroli, et al.
Pageof 3