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Eva Trevisson

Showing results (31-40 of 86) with videos related to

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Cancers|November 20, 2019
Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment RecommendationsMatteo Cassina, Luisa Frizziero, Enrico Opocher, et al.
Biochimica Et Biophysica Acta|October 22, 2013
Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiencyMara Doimo, Eva Trevisson, Rannar Airik, et al.
Cancers|March 25, 2022
Choroidal Abnormalities in Pediatric NF1: A Cohort Natural History StudyEleonora Cosmo, Luisa Frizziero, Giacomo Miglionico, et al.
Human Mutation|February 28, 2007
Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogeneEva Trevisson, Leonardo Salviati, Maria Cristina Baldoin, et al.
Molecular Genetics & Genomic Medicine|March 8, 2019
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromasEva Trevisson, Valeria Morbidoni, Monica Forzan, et al.
Retina (Philadelphia, Pa.)|August 25, 2020
RETINAL VASCULAR ABNORMALITIES RELATED TO NEUROFIBROMATOSIS TYPE 1: Natural History and Classification by Optical Coherence Tomography Angiography in 473 PatientsRaffaele Parrozzani, Luisa Frizziero, Sara Trainiti, et al.
The Journal of Biological Chemistry|August 26, 2009
Functional complementation in yeast allows molecular characterization of missense argininosuccinate lyase mutationsEva Trevisson, Alberto Burlina, Mara Doimo, et al.
Journal of Neuro-Oncology|June 4, 2017
Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1Eva Trevisson, Matteo Cassina, Enrico Opocher, et al.
Acta Ophthalmologica|October 5, 2018
Correlation of peripapillary retinal nerve fibre layer thickness with visual acuity in paediatric patients affected by optic pathway gliomaRaffaele Parrozzani, Giacomo Miglionico, Francesca Leonardi, et al.
Biochemical and Biophysical Research Communications|October 11, 2005
hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assemblySabrina Sacconi, Eva Trevisson, Francesca Pistollato, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
Cancers|November 20, 2019
Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment RecommendationsMatteo Cassina, Luisa Frizziero, Enrico Opocher, et al.
Biochimica Et Biophysica Acta|October 22, 2013
Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiencyMara Doimo, Eva Trevisson, Rannar Airik, et al.
Cancers|March 25, 2022
Choroidal Abnormalities in Pediatric NF1: A Cohort Natural History StudyEleonora Cosmo, Luisa Frizziero, Giacomo Miglionico, et al.
Human Mutation|February 28, 2007
Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogeneEva Trevisson, Leonardo Salviati, Maria Cristina Baldoin, et al.
Molecular Genetics & Genomic Medicine|March 8, 2019
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromasEva Trevisson, Valeria Morbidoni, Monica Forzan, et al.
Retina (Philadelphia, Pa.)|August 25, 2020
RETINAL VASCULAR ABNORMALITIES RELATED TO NEUROFIBROMATOSIS TYPE 1: Natural History and Classification by Optical Coherence Tomography Angiography in 473 PatientsRaffaele Parrozzani, Luisa Frizziero, Sara Trainiti, et al.
The Journal of Biological Chemistry|August 26, 2009
Functional complementation in yeast allows molecular characterization of missense argininosuccinate lyase mutationsEva Trevisson, Alberto Burlina, Mara Doimo, et al.
Journal of Neuro-Oncology|June 4, 2017
Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1Eva Trevisson, Matteo Cassina, Enrico Opocher, et al.
Acta Ophthalmologica|October 5, 2018
Correlation of peripapillary retinal nerve fibre layer thickness with visual acuity in paediatric patients affected by optic pathway gliomaRaffaele Parrozzani, Giacomo Miglionico, Francesca Leonardi, et al.
Biochemical and Biophysical Research Communications|October 11, 2005
hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assemblySabrina Sacconi, Eva Trevisson, Francesca Pistollato, et al.
Pageof 9