نتائج البحث - Mário Teruo Sato
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Distrofia retiniana com onda rápida escotópica (DRORE) associada à síndrome dos cabelos anágenos frouxos (SCAF). Parte II: Genética حسب Mário Teruo Sato, Rodrigo Marzagão, Nina Amália Brancia Pagnan, N. Freire‐Maia, Carlos Augusto Moreira Júnior
منشور في 2004Artigo -
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Epidemiological profile of age-related macular degeneration patients in Federal University of Parana, Brazil حسب Fernando Pradella, Renato Nisihara, Mário Teruo Sato, Alexandre Achille Grandinetti, Sergio B. Novello, Marcelo Pires, Diego José Schebelski, Iara Messias-Reason
منشور في 2016Artigo -
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New Insights on the Regulatory Gene Network Disturbed in Central Areolar Choroidal Dystrophy—Beyond Classical Gene Candidates حسب João Paulo Kazmierczak de Camargo, Giovanna Nazaré de Barros Prezia, Naoye Shiokawa, Mário Teruo Sato, Roberto Rosati, Angelica Beate Winter Boldt
منشور في 2022Revisão -
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Neurosyphilis and ocular syphilis clinical and cerebrospinal fluid characteristics: a case series حسب Conrado Regis Borges, Sérgio Monteiro de Almeida, Karen Sue, Jéssyca Luana Alves Koslyk, Mário Teruo Sato, Naoye Shiokawa, Hélio Afonso Ghizoni Teive
منشور في 2018Artigo -
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Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família حسب Mário Teruo Sato, Fabiane Mulinari Brenner, Rodrigo Marzagão, Fábio Sabbag, Gisele Bordignon, José Fillus Neto, Daura Regina Eiras-Stofella, Antonio Franco, Carlos Augusto Moreira Júnior
منشور في 2004Artigo -
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APLICAÇÃO DO MÉTODO "CAGE" PARA ESTUDO DA PREVALÊNCIA E DETECÇÃO PRECOCE DO ALCOOLISMO EM ENFERMARIASGERAIS E ESPECIALIZADAS DE UM HOSPITAL UNIVERSITÁRIO حسب Marilinda Bettina S.S Santos, Ademar Z. Gailit, Mário Teruo Sato, Marcos Lawrynink, Jean Boutros Sater, José Carlos Czpak, Luiz Fernando Ribas, Nelson de Andrade Oliveira
منشور في 1994Artigo -
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Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive Ataxias حسب Hélio Afonso Ghizoni Teive, Carlos Henrique Ferreira Camargo, Mário Teruo Sato, Naoye Shiokawa, César Luiz Boguszewski, Salmo Raskin, Cassandra Buck, Stephanie B. Seminara, Renato P. Munhoz
منشور في 2017Artigo -
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Descrição de nova distrofia macular associada à síndrome dos cabelos anágenos frouxos حسب Mário Teruo Sato, Rodrigo Marzagão, Christine Graff, Jaime Arana, Ana Tereza Ramos Moreira, Nina Amália Brancia Pagnan, Enilze Maria de Souza Fonseca Ribeiro, Carlos Augusto Moreira Júnior
منشور في 2002Artigo -
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Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction حسب Katarína Štingl, Britta Baumann, Pietro De Angeli, Ajoy Vincent, Elise Héon, Monique Cordonnier, Elfride De Baere, Salmo Raskin, Mário Teruo Sato, Naoye Shiokawa, Susanne Kohl, Bernd Wissinger
منشور في 2022Artigo -
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Therapeutic potential of human neural precursor cells in diabetic retinopathy—preclinical model حسب Cláudia Sayuri Saçaki, Bassam Felipe Mogharbel, Priscila Elias Ferreira Stricker, Dilcele Silva Moreira Dziedzic, Ana Carolina Irioda, Maiara Carolina Perussolo, Fabiano Montiani Ferreira, Juan Carlos Duque Moreno, Peterson Triches Dornbusch, Mário Teruo Sato, Naoye Shiokawa, Lúcia de Noronha, Marianna Bacelar Galdino, Eltyeb Abdelwahid, Célia Regina Cavichiolo Franco, Katherine Athayde Teixeira de Carvalho
منشور في 2021Artigo -
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Therapeutic Potential Of Human Neural Precursor Cells in Diabetic Retinopathy – Preclinical Model حسب Cláudia Sayuri Saçaki, Bassam Felipe Mogharbel, Priscila Elias Ferreira Stricker, Dilcele Silva Moreira Dziedzic, Ana Carolina Irioda, Maiara Carolina Perussolo, Fabiano Montiani‐Ferreira, Juan Carlos Duque Moreno, Peterson Triches Dornbusch, Mário Teruo Sato, Naoye Shiokawa, Lúcia de Noronha, Seigo Nagashima, Marianna Bacellar‐Galdino, Célia Regina Cavichiolo Franco, Eltyeb Abdelwahid, Katherine Athayde Teixeira de Carvalho
منشور في 2021Pré-impressão
أدوات البحث:
موضوعات ذات صلة
Medicine
Ophthalmology
Biology
Gene
Genetics
Pathology
Retinal
Diabetes mellitus
Electroretinography
Endocrinology
Internal medicine
Psychiatry
Ataxia
Diabetic retinopathy
Disease
Neuroscience
Phenotype
Retina
Allele
Compound heterozygosity
Computational biology
Erg
Gynecology
Humanities
Macular degeneration
Mutation
Optometry
Philosophy
Photoreceptor cell
Spinocerebellar ataxia