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Victor Ferraz
Victor Ferraz
Professor - Departamento de Genética da Faculdade de Medicina de Ribeirão Preto, Universidade de São
E-mail confirmado em usp.br
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Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis?
T Vieira, I Schwartz, V Munoz, L Pinto, C Steiner, M Ribeiro, R Boy, ...
American Journal of Medical Genetics Part A 146 (13), 1741-1747, 2008
1232008
Genetic services and testing in Brazil
DDG Horovitz, VE de Faria Ferraz, S Dain, AP Marques-de-Faria
Journal of community genetics 4, 355-375, 2013
1192013
Genetics and genomics in Brazil: a promising future
MR Passos-Bueno, D Bertola, DDG Horovitz, VE de Faria Ferraz, LA Brito
Molecular genetics & genomic medicine 2 (4), 280, 2014
692014
Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and Barber-Say syndromes
S Marchegiani, T Davis, F Tessadori, G Van Haaften, F Brancati, ...
The American Journal of Human Genetics 97 (1), 99-110, 2015
672015
Clinical genetics in developing countries: the case of Brazil
AP Marques-de-Faria, VEF Ferraz, AX Acosta, D Brunoni
Public Health Genomics 7 (2-3), 95-105, 2004
612004
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: Analysis of a 21 gene panel in the Brazilian population
S da Costa e Silva Carvalho, NM Cury, DB Brotto, LF De Araujo, ...
BMC medical genomics 13, 1-24, 2020
472020
Genetic education, knowledge and experiences between nurses and physicians in primary care in Brazil: A cross‐sectional study
LC Lopes‐Júnior, PM Carvalho Junior, VE de Faria Ferraz, ...
Nursing & health sciences 19 (1), 66-74, 2017
472017
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families
NM Cury, VEF Ferraz, WA Silva
Hereditary cancer in clinical practice 12, 1-8, 2014
392014
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil
MB de Melo, AK Mandal, IM Tavares, MH Ali, M Kabra, ...
PLoS One 10 (5), e0127147, 2015
282015
Obesidade infanto-juvenil: uma proposta de classificação clínica
CAN de Almeida, MEC Baptista, GAN de Almeida, VE de Faria Ferraz
Pediatria (São Paulo) 26 (4), 257-67, 2004
282004
Ablepharon‐macrostomia syndrome: First report of familial occurrence
VEF Ferraz, DG Melo, SE Hansing, AAV Cruz, JM Pina‐Neto
American journal of medical genetics 94 (4), 281-283, 2000
262000
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 …
M Flória-Santos, LC Lopes-Júnior, LM Alvarenga, MS Ribeiro, VEF Ferraz, ...
Genetics and molecular biology 39, 178-183, 2016
242016
Congenital shortening of the anterior lamella of all eyelids: the so-called ablepharon macrostomia syndrome
AAV Cruz, FC Guimarães, HN Obeid, VEF Ferraz, TR Noce, FE Martinez
Ophthalmic Plastic & Reconstructive Surgery 11 (4), 284-287, 1995
221995
Aggravation of eyelid and conjunctival malignancies following photodynamic therapy in DeSanctis-Cacchione syndrome
F Procianoy, AAV Cruz, A Baccega, V Ferraz, F Chahud
Ophthalmic Plastic & Reconstructive Surgery 22 (6), 498-499, 2006
212006
Percepção de causas e risco oncológico, história familiar e comportamentos preventivos de usuários em aconselhamento oncogenético
TBC Silva, DJ MacDonald, VEF Ferraz, LC Nascimento, CB Santos, ...
Revista da Escola de Enfermagem da USP 47, 377-384, 2013
202013
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect
GA De Molfetta, TM Felix, M Riegel, VEF Ferraz, JM Pina Neto
Arquivos de Neuro-Psiquiatria 60, 1011-1014, 2002
202002
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries
EM Monteiro Santos, MD Valentin, F Carneiro, LP de Oliveira, ...
BMC cancer 12, 1-9, 2012
142012
Familial occurrence of ablepharon macrostomia syndrome: eyelid structure and surgical considerations
AAV Cruz, CA Souza, VEF Ferraz, CAC Monteiro, FA Martins
Archives of ophthalmology 118 (3), 429-430, 2000
142000
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN)
TM Félix, BM de Oliveira, M Artifon, I Carvalho, FA Bernardi, IVD Schwartz, ...
Orphanet Journal of Rare Diseases 17 (1), 84, 2022
132022
Perception of cancer causes and risk, family history and preventive behaviors of users in oncogenetic counseling
DJ MacDonald, VEF Ferraz, LC Nascimento, CB Santos, LC Lopes-Júnior, ...
Revista da Escola de Enfermagem da USP 47, 377-384, 2013
132013
O sistema não pode executar a operação agora. Tente novamente mais tarde.
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