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Showing results (171-180 of 190) with videos related to

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Nature|April 13, 2018
Anomalously weak Labrador Sea convection and Atlantic overturning during the past 150 yearsDavid J R Thornalley, Delia W Oppo, Pablo Ortega, et al.
Msystems|September 16, 2020
Gut Microbiota and Metabolome Alterations Associated with Parkinson's DiseaseSarah Vascellari, Vanessa Palmas, Marta Melis, et al.
Neuromuscular Disorders : NMD|October 14, 2011
Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophyNicola Carboni, Marco Mura, Eugenio Mercuri, et al.
Plos Pathogens|June 30, 2023
α-Synuclein seeding activity in duodenum biopsies from Parkinson's disease patientsSarah Vascellari, Christina D Orrù, Bradley R Groveman, et al.
Metabolism: Clinical and Experimental|September 10, 2015
Mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophiesFrederic Reinier, Magdalena Zoledziewska, David Hanna, et al.
Journal of Human Genetics|October 14, 2016
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in OmanFlavia Palombo, Nadia Al-Wardy, Guido Alberto Gnecchi Ruscone, et al.
Journal of Neurology|December 23, 2020
Levodopa-carbidopa intrajejunal infusion in Parkinson's disease: untangling the role of ageFrancesca Morgante, Valentina Oppo, Margherita Fabbri, et al.
BMC Medical Genetics|January 16, 2019
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case reportRita Maria Alves, Paolo Uva, Marielza F Veiga, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2015
Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive OsteopetrosisEleonora Palagano, Harry C Blair, Alessandra Pangrazio, et al.
Clinical Genetics|March 13, 2019
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnosesAndrea Angius, Paolo Uva, Manuela Oppo, et al.
Pageof 19

Showing results (171-180 of 190) with videos related to

Sort By:
Pageof 19
Nature|April 13, 2018
Anomalously weak Labrador Sea convection and Atlantic overturning during the past 150 yearsDavid J R Thornalley, Delia W Oppo, Pablo Ortega, et al.
Msystems|September 16, 2020
Gut Microbiota and Metabolome Alterations Associated with Parkinson's DiseaseSarah Vascellari, Vanessa Palmas, Marta Melis, et al.
Neuromuscular Disorders : NMD|October 14, 2011
Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophyNicola Carboni, Marco Mura, Eugenio Mercuri, et al.
Plos Pathogens|June 30, 2023
α-Synuclein seeding activity in duodenum biopsies from Parkinson's disease patientsSarah Vascellari, Christina D Orrù, Bradley R Groveman, et al.
Metabolism: Clinical and Experimental|September 10, 2015
Mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophiesFrederic Reinier, Magdalena Zoledziewska, David Hanna, et al.
Journal of Human Genetics|October 14, 2016
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in OmanFlavia Palombo, Nadia Al-Wardy, Guido Alberto Gnecchi Ruscone, et al.
Journal of Neurology|December 23, 2020
Levodopa-carbidopa intrajejunal infusion in Parkinson's disease: untangling the role of ageFrancesca Morgante, Valentina Oppo, Margherita Fabbri, et al.
BMC Medical Genetics|January 16, 2019
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case reportRita Maria Alves, Paolo Uva, Marielza F Veiga, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2015
Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive OsteopetrosisEleonora Palagano, Harry C Blair, Alessandra Pangrazio, et al.
Clinical Genetics|March 13, 2019
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnosesAndrea Angius, Paolo Uva, Manuela Oppo, et al.
Pageof 19