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G Parenti

Showing results (131-140 of 226) with videos related to

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Biochemistry|February 27, 1996
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particlesR Fato, E Estornell, S Di Bernardo, et al.
Rivista Di Neurologia|May 1, 1986
[Relation between neurologic damage and collateral circulation detected by Doppler CW in occlusive pathology of the internal carotid]C Giraldi, L Volpentesta, M Manetti, et al.
Journal of Cardiovascular Pharmacology|August 15, 2000
Antioxidant effect of oral dipyridamole during cerebral hypoperfusion with human carotid endarterectomyC Kusmic, C Petersen, E Picano, et al.
Radiology Case Reports|February 15, 2020
Imaging findings in Möbius-Poland syndromeVincent G Parenti, Xiaozhou Liu, Akshita Mehta, et al.
Human Genetics|December 1, 1987
Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 12, 2007
Genetics and biology of pheochromocytomaM Mannelli, L Simi, M S Gaglianò, et al.
European Journal of Pediatrics|July 1, 1987
Evidence of polyglandular involvement in Niemann-Pick disease type BP Strisciuglio, S Di Maio, G Parenti, et al.
American Journal of Medical Genetics|August 10, 1999
Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate formL Titomanlio, R Della Casa, M Lecora, et al.
Human Genetics|March 1, 1986
X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.
Clinical Genetics|July 3, 1998
A novel mutation of the beta-glucocerebrosidase gene associated with neurologic manifestations in three sibsG Parenti, M Filocamo, L Titomanlio, et al.
Pageof 23

Showing results (131-140 of 226) with videos related to

Sort By:
Pageof 23
Biochemistry|February 27, 1996
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particlesR Fato, E Estornell, S Di Bernardo, et al.
Rivista Di Neurologia|May 1, 1986
[Relation between neurologic damage and collateral circulation detected by Doppler CW in occlusive pathology of the internal carotid]C Giraldi, L Volpentesta, M Manetti, et al.
Journal of Cardiovascular Pharmacology|August 15, 2000
Antioxidant effect of oral dipyridamole during cerebral hypoperfusion with human carotid endarterectomyC Kusmic, C Petersen, E Picano, et al.
Radiology Case Reports|February 15, 2020
Imaging findings in Möbius-Poland syndromeVincent G Parenti, Xiaozhou Liu, Akshita Mehta, et al.
Human Genetics|December 1, 1987
Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 12, 2007
Genetics and biology of pheochromocytomaM Mannelli, L Simi, M S Gaglianò, et al.
European Journal of Pediatrics|July 1, 1987
Evidence of polyglandular involvement in Niemann-Pick disease type BP Strisciuglio, S Di Maio, G Parenti, et al.
American Journal of Medical Genetics|August 10, 1999
Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate formL Titomanlio, R Della Casa, M Lecora, et al.
Human Genetics|March 1, 1986
X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.
Clinical Genetics|July 3, 1998
A novel mutation of the beta-glucocerebrosidase gene associated with neurologic manifestations in three sibsG Parenti, M Filocamo, L Titomanlio, et al.
Pageof 23