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Francesca Pasutto

Showing results (1-10 of 56) with videos related to

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Investigative Ophthalmology & Visual Science|November 22, 2021
Perifoveal Cone- and Rod-Mediated Temporal Contrast Sensitivities in Stargardt Disease/Fundus FlavimaculatusJulien Fars, Francesca Pasutto, Jan Kremers, et al.
Ophthalmic Genetics|September 28, 2018
Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophyFrancesca Pasutto, Arif Ekici, André Reis, et al.
Genes|April 3, 2021
An Assessment of GUCA1C Variants in Primary Congenital GlaucomaEmmanuelle Souzeau, Nicole Weisschuh, Jamie E Craig, et al.
BMC Genetics|January 30, 2010
Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German populationChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Investigative Ophthalmology & Visual Science|September 28, 2011
Regulation of lysyl oxidase-like 1 (LOXL1) and elastin-related genes by pathogenic factors associated with pseudoexfoliation syndromeMatthias Zenkel, Anita Krysta, Francesca Pasutto, et al.
Journal of Glaucoma|April 18, 2009
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucomaChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
BMC Medical Genetics|September 17, 2009
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control studyChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect (PDAC) syndrome due to STRA6 mutations--what are the minimal criteria?Reeval Segel, Ephrat Levy-Lahad, Francesca Pasutto, et al.
Human Mutation|May 13, 2008
Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzymeGabriela Chavarria-Soley, Heinrich Sticht, Eleni Aklillu, et al.
Pageof 6

Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Investigative Ophthalmology & Visual Science|November 22, 2021
Perifoveal Cone- and Rod-Mediated Temporal Contrast Sensitivities in Stargardt Disease/Fundus FlavimaculatusJulien Fars, Francesca Pasutto, Jan Kremers, et al.
Ophthalmic Genetics|September 28, 2018
Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophyFrancesca Pasutto, Arif Ekici, André Reis, et al.
Genes|April 3, 2021
An Assessment of GUCA1C Variants in Primary Congenital GlaucomaEmmanuelle Souzeau, Nicole Weisschuh, Jamie E Craig, et al.
BMC Genetics|January 30, 2010
Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German populationChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Investigative Ophthalmology & Visual Science|September 28, 2011
Regulation of lysyl oxidase-like 1 (LOXL1) and elastin-related genes by pathogenic factors associated with pseudoexfoliation syndromeMatthias Zenkel, Anita Krysta, Francesca Pasutto, et al.
Journal of Glaucoma|April 18, 2009
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucomaChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
BMC Medical Genetics|September 17, 2009
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control studyChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect (PDAC) syndrome due to STRA6 mutations--what are the minimal criteria?Reeval Segel, Ephrat Levy-Lahad, Francesca Pasutto, et al.
Human Mutation|May 13, 2008
Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzymeGabriela Chavarria-Soley, Heinrich Sticht, Eleni Aklillu, et al.
Pageof 6