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A Rufa

Showing results (31-40 of 36) with videos related to

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Journal of Submicroscopic Cytology and Pathology|December 16, 1998
Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic studyA Federico, M T Dotti, E Cardaioli, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
Journal of Neurology|February 20, 2010
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiaritiesS Bianchi, A Rufa, M Ragno, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Neuroscience|March 23, 2016
Visual impairment in FOXG1-mutated individuals and miceE M Boggio, L Pancrazi, M Gennaro, et al.
Science (New York, N.Y.)|November 9, 2023
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitorsMelissa L Boby, Daren Fearon, Matteo Ferla, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Submicroscopic Cytology and Pathology|December 16, 1998
Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic studyA Federico, M T Dotti, E Cardaioli, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
Journal of Neurology|February 20, 2010
High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiaritiesS Bianchi, A Rufa, M Ragno, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Neuroscience|March 23, 2016
Visual impairment in FOXG1-mutated individuals and miceE M Boggio, L Pancrazi, M Gennaro, et al.
Science (New York, N.Y.)|November 9, 2023
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitorsMelissa L Boby, Daren Fearon, Matteo Ferla, et al.
Pageof 4