Professor de Genética Clínica da Pontifícia Universidade Católica de Campinas-SP (Puccamp);
Membro da Câmara Técnica de Doenças Raras do Conselho Federal de Medicina (CFM).
Graduado em Medicina pela Universidade Federal do Amazonas (UFAM) em 2003.
Residência Médica em Pediatria no Hospital Infantil Cândido Fontoura em 2006;
Residência Médica em Genética Médica no Hospital São Paulo da Universidade Federal de São Paulo (Unifesp) em 2009.
Mestre em Ciências pela Faculdade de Medicina da Universidade de São Paulo em 2015.
Título de Genética pela Sociedade Brasileira de Genética Médica.
FRANCO, JOSÉ FRANCISCO DA SILVA; EL DIB, REGINA ; AGARWAL, ARNAV ; SOARES, DIOGO ; MILHAN, NOALA VICENSOTO MOREIRA ; ALBANO, LILIAN MARIA JOSÉ ; KIM, CHONG AE . Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy: Results from a single-center case series study. Intractable & Rare Diseases Research, v. 6, p. 183-190, 2017.
PAOLACCI, STEFANO ; BERTOLA, DEBORA ; FRANCO, JOSÉ ; MOHAMMED, SHEHLA ; TARTAGLIA, MARCO ; WOLLNIK, BERND ; HENNEKAM, RAOUL C. . Wiedemann-Rautenstrauch syndrome: A phenotype analysis. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 173, p. 1763-1772, 2017.
MONTAÑO, ADRIANA M LOCK-HOCK, NGU STEINER, ROBERT D GRAHAM, BRETT H SZLAGO, MARINA GREENSTEIN, ROBERT PINEDA, MERCEDES GONZALEZ-MENESES, ANTONIO ÇOKER, MAHMUT BARTHOLOMEW, DENNIS SANDS, MARK S WANG, RAYMOND GIUGLIANI, ROBERTO MACAYA, ALFONS PASTORES, GREGORY KETKO, ANASTASIA K EZGÜ, FATIH TANAKA, AKEMI ARASH, LAILA BECK, MICHAEL FALK, RENA E BHATTACHARYA, KAUSTUV FRANCO, JOSÉ WHITE, KLANE K MITCHELL, GRANT A , et al. ; Clinical course of sly syndrome (mucopolysaccharidosis type VII). JOURNAL OF MEDICAL GENETICS, v. 53, p. 403-418, 2016. Citações:1|7
FRANCO, J.F.; SOARES, D.C. ; TORRES, L.C. ; LEAL, G.N. ; CUNHA, M.T. ; HONJO, R.S. ; BERTOLA, D.R. ; KIM, C.A. . Short Communication Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings. GENETICS AND MOLECULAR RESEARCH, v. 15, p. 1-7, 2016.
ARANDA, CAROLINA ; MAGALHÃES, TATIANA DE SÁ PACHECO C. ; FRANCO, JOSÉ FRANCISCO ; ENSINA, LUIS FELIPE C. ; DE LACERDA, ALEX E. ; MARTINS, ANA MARIA . Laronidase hypersensitivity and desensitization of mucopolysaccharidosis I (Scheie syndrome) patient. MOLECULAR GENETICS AND METABOLISM, v. 117, p. S21-S22, 2016.
BORLOT, FELIPPE ; ARANTES, PAULA RICCI ; QUAIO, CAIO ROBLEDO ; FRANCO, JOSÉ FRANCISCO DA SILVA ; LOURENÇO, CHARLES MARQUES ; GOMY, ISRAEL ; BERTOLA, DEBORA ROMEO ; KIM, CHONG AE . Mucopolysaccharidosis type IVA: Evidence of primary and secondary central nervous system involvement. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 164, p. 1162-1169, 2014.
TORRES, LEURIDAN CAVALCANTE ; DE QUEIROZ SOARES, DIOGO CORDEIRO ; KULIKOWSKI, LESLIE DOMENICI ; Franco, Jose Francisco ; KIM, CHONG AE . NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene. CLINICAL IMMUNOLOGY, v. 154, p. 100-104, 2014.
BORLOT, FELIPPE ; ARANTES, PAULA RICCI ; QUAIO, CAIO ROBLEDO ; DA SILVA FRANCO, JOSÉ FRANCISCO ; LOURENÇO, CHARLES MARQUES ; BERTOLA, DEBORA ROMEO ; KIM, CHONG AE . New insights in mucopolysaccharidosis type VI: Neurological perspective. BRAIN & DEVELOPMENT, v. 7, p. Aug;36(7):585-9, 2013.
GOMES, C. Z. ; COURROL, L. C. ; FRANCO, JOSÉ FRANCISCO DA SILVA ; MARUMO, M. H. B. . Fluorescent study of human blood plasma albumin in diabetic patients. Journal of Biological Reasearch, v. 1, p. 1, 2012.
Atraso do desenvolvimento neuropsicomotor, deficiência intelectual, dismorfologia, erros intatos do metabolismo e aconselhamento genético.
, v. 173, p. 1763-1772, 2017.
1|
7
