Publications by authors named "Victor Ferraz"

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Therapeutic benefit of idebenone in Leber hereditary optic neuropathy: a systematic review and meta-analysis.
Paulo Victor Zattar Ribeiro, Lucas Pari Mitre, Mateus M Gauza, Paulo Henrique Furukawa, Victor Evangelista De Faria Ferraz

Ophthalmic Genet· December 2025

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Promoting Comprehensive Care for People With Rare Diseases in a Tertiary Care Setting in Brazil: Protocol for a Mixed Methods Implementation Study.
Domingos Alves, Filipe Andrade Bernardi, Vinicius Costa Lima, Diego Bettiol Yamada, Tatiana Takahasi Komoto, Victor Evangelista de Faria Ferraz

JMIR Res Protoc· August 2025

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Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies.
Dafne Dain Gandelman Horovitz, Têmis Maria Félix, Victor Evangelista de Faria Ferraz

Genes (Basel)· July 2024

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Importance of genetic cancer risk assessment as a strategy to stratify risk and provide precision prevention in high-risk patients and families.
Patricia Ashton-Prolla, Maria Isabel Waddington Achatz, Miguel Angelo Martins Moreira, Edenir Inez Palmero, Diogo Cordeiro de Queiroz Soares, Victor Evangelista de Faria Ferraz

Rev Assoc Med Bras (1992)· June 2024

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Risk for Hereditary Neoplastic Syndromes in Women with Mismatch Repair-Proficient Endometrial Cancer.
Jennifer Thalita Targino Dos Santos, Reginaldo Cruz Alves Rosa, Alison Luis Eburneo Pereira, Alan Vinicius Assunção-Luiz, Bruna Tavares Bacalá, Victor Evangelista de Faria Ferraz

Genes (Basel)· October 2023

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Health Policies for Rare Disease Patients: A Scoping Review.
Luís Carlos Lopes-Júnior, Victor Evangelista Faria Ferraz, Regina Aparecida Garcia Lima, Sara Isabel Pimentel Carvalho Schuab, Raphael Manhães Pessanha

Int J Environ Res Public Health· November 2022

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Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1.
Luiz Guilherme Darrigo Junior, Victor Evangelista de Faria Ferraz, Marina Candido Visontai Cormedi, Luissa Hikari Hayashi Araujo, Mariana Prado Silva Magalhães

Brain Behav· June 2022

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Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
Têmis Maria Félix, Bibiana Mello de Oliveira, Milena Artifon, Isabelle Carvalho, Filipe Andrade Bernardi, Victor E F Ferraz

Orphanet J Rare Dis· February 2022

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Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach.
Reginaldo Cruz Alves Rosa, Jessica Oliveira Santis, Lorena Alves Teixeira, Greice Andreotti Molfetta, Jennifer Thalita Targino Dos Santos, Victor Evangelista de Faria Ferraz

Gynecol Oncol· October 2020

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First description of ultramutated endometrial cancer caused by germline loss-of-function and somatic exonuclease domain mutations in POLE gene.
Reginaldo Cruz Alves Rosa, Andrey A Yurchenko, Fernando Chahud, Alfredo Ribeiro-Silva, Mariângela Ottoboni Brunaldi, Victor Evangelista de Faria Ferraz

Genet Mol Biol· September 2020

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Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.
Luiza Ferreira Araujo, Greice Andreotti Molfetta, Otavio Costa Vincenzi, Jair Huber, Lorena Alves Teixeira, Victor Evangelista Ferraz

Int J Biol Markers· March 2019

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Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
Simone da Costa E Silva Carvalho, Carlos Henrique Paiva Grangeiro, Clarissa Gondim Picanço-Albuquerque, Thaís Oliveira Dos Anjos, Greice Andreotti De Molfetta, Victor Evangelista de Faria Ferraz

BMC Res Notes· August 2018

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Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study.
Milena Flória-Santos, Luís Carlos Lopes-Júnior, Larissa de Melo Alvarenga, Mayara Segundo Ribeiro, Victor Evangelista de Faria Ferraz

Genet Mol Biol· June 2016

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Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.
Mônica Barbosa de Melo, Anil K Mandal, Ivan M Tavares, Mohammed Hasnat Ali, Meha Kabra, Victor E F Ferraz

PLoS One· April 2016

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Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.
Shannon Marchegiani, Taylor Davis, Federico Tessadori, Gijs van Haaften, Francesco Brancati, Victor Ferraz

Am J Hum Genet· July 2015

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[How the gynecologist can guide women with a family history of cancer?].
Victor Evangelista de Faria Ferraz, Nathalia Moreno Cury

Rev Bras Ginecol Obstet· August 2014

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TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families.
Nathalia M Cury, Victor Ef Ferraz, Wilson A Silva

Hered Cancer Clin Pract· March 2014

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Anterior cruciate ligament femoral socket drilling with a retrograde reamer: lessons from the learning curve.
Victor Ferraz, Paul Westerberg, Jefferson C Brand

Arthrosc Tech· January 2014

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Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.
Denny Schanze, Magdalena Harakalova, Cathy A Stevens, Francesco Brancati, Bruno Dallapiccola, Victor E F Ferraz

Am J Med Genet A· December 2013

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[Perception of cancer causes and risk, family history and preventive behaviors of users in oncogenetic counseling].
Tiago Barreto de Castro E Silva, Deborah J Macdonald, Victor Evangelista de Faria Ferraz, Lucila Castanheira Nascimento, Cláudia Benedita Dos Santos

Rev Esc Enferm USP· April 2013

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Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: Beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities.
Camila C Rebelo, João Mf Furtado, Rachel S Honjo, Kledione F Veiga, Ester S Ramos, Victor Ef Ferraz

Clin Dysmorphol· July 2009

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Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis?
Taiane Vieira, Ida Schwartz, Verónica Muñoz, Louise Pinto, Carlos Steiner, Victor Ferraz

Am J Med Genet A· July 2008

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Aggravation of eyelid and conjunctival malignancies following photodynamic therapy in DeSanctis-Cacchione syndrome.
Fernando Procianoy, Antonio A V Cruz, Adriano Baccega, Victor Ferraz, Fernando Chahud

Ophthalmic Plast Reconstr Surg· January 2007

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Clinical genetics in developing countries: the case of Brazil.
Antonia Paula Marques-de-Faria, Victor E Faria Ferraz, Angelina Xavier Acosta, Décio Brunoni

Community Genet· April 2005

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A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.
Greice Andreotti De Molfetta, Temis Maria Felix, Mariluce Riegel, Victor Evangelista de Faria Ferraz, João Monteiro de Pina Neto

Arq Neuropsiquiatr· December 2002

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