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Mario Teruo Sato

Showing results (1-10 of 9) with videos related to

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Arquivos Brasileiros De Oftalmologia|February 10, 2021
Clinical and electroretinographic profile of 27 patients with Stargardt disease treated at a hospital in BrazilLetícia Schemberger Schafranski, Izabelle Yumi Honda Müller, Mario Teruo Sato
Frontiers in Genetics|June 3, 2022
New Insights on the Regulatory Gene Network Disturbed in Central Areolar Choroidal Dystrophy-Beyond Classical Gene CandidatesJoão Paulo Kazmierczak de Camargo, Giovanna Nazaré de Barros Prezia, Naoye Shiokawa, et al.
Arquivos De Neuro-Psiquiatria|July 5, 2018
Neurosyphilis and ocular syphilis clinical and cerebrospinal fluid characteristics: a case seriesConrado Regis Borges, Sérgio Monteiro de Almeida, Karen Sue, et al.
Veterinary Ophthalmology|March 6, 2023
Preliminary characterization of a novel form of progressive retinal atrophy in the German Spitz dog associated with a frameshift mutation in GUCY2DMariza Bortolini, Paige A Winkler, Juan Carlos Duque Moreno, et al.
Cerebellum (London, England)|December 18, 2017
Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive AtaxiasHélio Afonso Ghizoni Teive, Carlos Henrique F Camargo, Mario Teruo Sato, et al.
Veterinary Ophthalmology|November 30, 2016
Characterization of a novel form of progressive retinal atrophy in Whippet dogs: a clinical, electroretinographic, and breeding studyAndré Tavares Somma, Juan Carlos Duque Moreno, Mario Teruo Sato, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
European Archives of Psychiatry and Clinical Neuroscience|March 17, 2023
Retinal layers and symptoms and inflammation in schizophreniaMarcelo Alves Carriello, Diogo F Bornancin Costa, Pedro Henrique Pereira Alvim, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Arquivos Brasileiros De Oftalmologia|February 10, 2021
Clinical and electroretinographic profile of 27 patients with Stargardt disease treated at a hospital in BrazilLetícia Schemberger Schafranski, Izabelle Yumi Honda Müller, Mario Teruo Sato
Frontiers in Genetics|June 3, 2022
New Insights on the Regulatory Gene Network Disturbed in Central Areolar Choroidal Dystrophy-Beyond Classical Gene CandidatesJoão Paulo Kazmierczak de Camargo, Giovanna Nazaré de Barros Prezia, Naoye Shiokawa, et al.
Arquivos De Neuro-Psiquiatria|July 5, 2018
Neurosyphilis and ocular syphilis clinical and cerebrospinal fluid characteristics: a case seriesConrado Regis Borges, Sérgio Monteiro de Almeida, Karen Sue, et al.
Veterinary Ophthalmology|March 6, 2023
Preliminary characterization of a novel form of progressive retinal atrophy in the German Spitz dog associated with a frameshift mutation in GUCY2DMariza Bortolini, Paige A Winkler, Juan Carlos Duque Moreno, et al.
Cerebellum (London, England)|December 18, 2017
Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive AtaxiasHélio Afonso Ghizoni Teive, Carlos Henrique F Camargo, Mario Teruo Sato, et al.
Veterinary Ophthalmology|November 30, 2016
Characterization of a novel form of progressive retinal atrophy in Whippet dogs: a clinical, electroretinographic, and breeding studyAndré Tavares Somma, Juan Carlos Duque Moreno, Mario Teruo Sato, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
European Archives of Psychiatry and Clinical Neuroscience|March 17, 2023
Retinal layers and symptoms and inflammation in schizophreniaMarcelo Alves Carriello, Diogo F Bornancin Costa, Pedro Henrique Pereira Alvim, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Pageof 1