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V Carelli

Showing results (61-70 of 104) with videos related to

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Current Molecular Medicine|October 18, 2014
Genetic Basis of Mitochondrial Optic NeuropathiesA Maresca, L Caporali, D Strobbe, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Cephalalgia : an International Journal of Headache|December 1, 1993
Testing models for genetic determination in migraineM Mochi, S Sangiorgi, P Cortelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathyR Lodi, V Carelli, P Cortelli, et al.
Biochimica Et Biophysica Acta|January 8, 1991
1H-NMR study and structure determination of 4,4- and 4,6-dimers from electrochemical reduction of NADP+E Ragg, L Scaglioni, R Mondelli, et al.
BMC Neurology|January 1, 2020
Functional MRI study in a case of Charles Bonnet syndrome related to LHONV Vacchiano, C Tonon, M Mitolo, et al.
Journal of the Neurological Sciences|December 16, 1998
Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientV Carelli, P Barboni, A Zacchini, et al.
The International Journal of Neuroscience|June 4, 2021
Behavior and electrophysiological effects on striatum-nigra circuit after high frequency stimulation. Relevance to Parkinson and epilepsyIgor Tchaikovsky, Marilia Marinho Lucena, Belmira-Lara da Silveira Andrade da Costa, et al.
Epilepsia|June 1, 1997
Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic studyA Parmeggiani, A E Lehesjoki, V Carelli, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Current Molecular Medicine|October 18, 2014
Genetic Basis of Mitochondrial Optic NeuropathiesA Maresca, L Caporali, D Strobbe, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Cephalalgia : an International Journal of Headache|December 1, 1993
Testing models for genetic determination in migraineM Mochi, S Sangiorgi, P Cortelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathyR Lodi, V Carelli, P Cortelli, et al.
Biochimica Et Biophysica Acta|January 8, 1991
1H-NMR study and structure determination of 4,4- and 4,6-dimers from electrochemical reduction of NADP+E Ragg, L Scaglioni, R Mondelli, et al.
BMC Neurology|January 1, 2020
Functional MRI study in a case of Charles Bonnet syndrome related to LHONV Vacchiano, C Tonon, M Mitolo, et al.
Journal of the Neurological Sciences|December 16, 1998
Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientV Carelli, P Barboni, A Zacchini, et al.
The International Journal of Neuroscience|June 4, 2021
Behavior and electrophysiological effects on striatum-nigra circuit after high frequency stimulation. Relevance to Parkinson and epilepsyIgor Tchaikovsky, Marilia Marinho Lucena, Belmira-Lara da Silveira Andrade da Costa, et al.
Epilepsia|June 1, 1997
Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic studyA Parmeggiani, A E Lehesjoki, V Carelli, et al.
Pageof 11