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P Barboni

Showing results (21-30 of 33) with videos related to

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Human Immunology|December 1, 1990
Reassessment of HLA association with celiac disease in special reference to the DP associationM Colonna, W Mantovani, G R Corazza, 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.
Neurology|August 1, 1991
Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian familyP Cortelli, P Montagna, P Avoni, et al.
Neurology|July 1, 1995
Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutationB Barbiroli, P Montagna, P Cortelli, 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.
Tissue Antigens|October 1, 1992
HLA-DP polymorphism in northern Italian celiac patientsV Mantovani, G R Corazza, M Frisoni, et al.
Journal of the Neurological Sciences|May 1, 1997
Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS studyP Cortelli, P Montagna, G Pierangeli, et al.
Clinical and Experimental Immunology|January 1, 1991
Molecular analysis of HLA-DQ A alleles in coeliac disease lack of a unique disease-associated sequenceV Mantovani, G R Corazza, G Angelini, et al.
Journal of Medical Genetics|July 4, 2006
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotypeM L Valentino, P Barboni, C Rengo, et al.
American Journal of Human Genetics|May 1, 1997
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484A Torroni, M Petrozzi, L D'Urbano, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Human Immunology|December 1, 1990
Reassessment of HLA association with celiac disease in special reference to the DP associationM Colonna, W Mantovani, G R Corazza, 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.
Neurology|August 1, 1991
Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian familyP Cortelli, P Montagna, P Avoni, et al.
Neurology|July 1, 1995
Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutationB Barbiroli, P Montagna, P Cortelli, 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.
Tissue Antigens|October 1, 1992
HLA-DP polymorphism in northern Italian celiac patientsV Mantovani, G R Corazza, M Frisoni, et al.
Journal of the Neurological Sciences|May 1, 1997
Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS studyP Cortelli, P Montagna, G Pierangeli, et al.
Clinical and Experimental Immunology|January 1, 1991
Molecular analysis of HLA-DQ A alleles in coeliac disease lack of a unique disease-associated sequenceV Mantovani, G R Corazza, G Angelini, et al.
Journal of Medical Genetics|July 4, 2006
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotypeM L Valentino, P Barboni, C Rengo, et al.
American Journal of Human Genetics|May 1, 1997
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484A Torroni, M Petrozzi, L D'Urbano, et al.
Pageof 4