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Eny Maria Goloni-Bertollo

Research Profile

Chemicals & Drugs

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Brazil

Procedures

Physiology

Disorders

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Infants

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Publications

TOP 3
Cristiani Cortez Mendes; Luciana Dutra Oliveira; Aline Maria Zanchetta de Aquino Raimundo; Maria Francesca Riccio; Helio Vannucchi; Bruna Lancia Zampieri; Joice Matos Biselli; Valdemir Melechco Carvalho; MN Eberlin; Eny Maria Goloni-Bertollo; R Haddad; Gustavo Henrique Marucci; Érika Cristina Pavarino
DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with down syndrome.
A L S Galbiatti; E C Pavarino; J A Padovani; H C Caldas; Eny Maria Goloni-Bertollo
Sensitivity of human laryngeal squamous cell carcinoma Hep-2 to metrotexate chemoterapy.
Joice Matos Biselli; Valdemir Carvalho; Marcos N Eberlin; M F R Fonseca; Eny Maria Goloni-Bertollo; R Haddad; Helio Vannucchi; B L Zampieri; E C Pavarino
Genetic polymorphisms modulate the folate metabolism of Brazilian individuals with Down syndrome.

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All Publications

2013: Cristiani Cortez Mendes; Luciana Dutra Oliveira; Aline Maria Zanchetta de Aquino Raimundo; Maria Francesca Riccio; Helio Vannucchi; Bruna Lancia Zampieri; Joice Matos Biselli; Valdemir Melechco Carvalho; MN Eberlin; Eny Maria Goloni-Bertollo; R Haddad; Gustavo Henrique Marucci; Érika Cristina Pavarino
DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with down syndrome.
Genetic testing and molecular biomarkers 2013;17(4):274-7.
2012: A L S Galbiatti; E C Pavarino; J A Padovani; H C Caldas; Eny Maria Goloni-Bertollo
Sensitivity of human laryngeal squamous cell carcinoma Hep-2 to metrotexate chemoterapy.
Experimental oncology 2012;34(4):367-9.
2012: Joice Matos Biselli; Valdemir Carvalho; Marcos N Eberlin; M F R Fonseca; Eny Maria Goloni-Bertollo; R Haddad; Helio Vannucchi; B L Zampieri; E C Pavarino
Genetic polymorphisms modulate the folate metabolism of Brazilian individuals with Down syndrome.
Molecular biology reports 2012;39(10):9277-84.
2012: Ana Lívia Silva Galbiatti; José Victor Maníglia; Erika Cristina Pavarino; Luis Sérgio Raposo; Mariangela Torreglosa Ruiz-Cintra; Lidia Maria Rebolho Batista da Silva; Eny Maria Goloni-Bertollo
Association between 11 genetic polymorphisms in folate-metabolising genes and head and neck cancer risk.
European journal of cancer (Oxford, England : 1990) 2012;48(10):1525-31.
2012: Bruna Lancia Zampieri; Joice Matos Biselli; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino
BHMT G742A and MTHFD1 G1958A polymorphisms and Down syndrome risk in the Brazilian population.
Genetic testing and molecular biomarkers 2012;16(6):628-31.
2012: Mariângela Torreglosa Ruiz; Ana Lívia Silva Galbiatti; José Victor Maniglia; Erika Cristina Pavarino; Eny Maria Goloni-Bertollo
Q36R polymorphism of KiSS-1 gene in Brazilian head and neck cancer patients.
Molecular biology reports 2012;39(5):6029-34.
2012: P M Biselli-Chicote; A R C P Oliveira; E C Pavarino; Eny Maria Goloni-Bertollo
VEGF gene alternative splicing: pro- and anti-angiogenic isoforms in cancer.
Journal of cancer research and clinical oncology 2012;138(3):363-70.
2012: Ana Lívia Silva Galbiatti; José Victor Maniglia; Erika Cristina Pavarino-Bertelli; Luis Sérgio Raposo; Mariangela Torreglosa Ruiz; Eny Maria Goloni-Bertollo
Head and neck cancer: genetic polymorphisms and folate metabolism.
Brazilian journal of otorhinolaryngology 2012;78(1):132-9.
2012: Maurício José Cabral Ruback; Mariangela Torreglosa Ruiz-Cintra; Anelise Russo; Lidia Maria Rebolho Batista Arantes; Ana Lívia Galbiatti; José Victor Maniglia; Gustavo Henrique Marucci; Erika Cristina Pavarino; Luiz Sérgio Raposo; Eny Maria Goloni-Bertollo
Clinical and epidemiological characteristics of patients in the head and neck surgery department of a university hospital.
São Paulo medical journal = Revista paulista de medicina 2012;130(5):307-13.
2012: Bruna Lancia Zampieri; Helio Vannucchi; Joice Matos Biselli; Valdemir Carvalho; José Antônio Cordeiro; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino
Maternal risk for Down syndrome is modulated by genes involved in folate metabolism.
Disease markers 2012;32(2):73-81.
2012: Ana Lívia Silva Galbiatti; José Victor Maníglia; Érika Cristina Pavarino; Luiz Sérgio Raposo; Juliana Olsen Rodrigues; Mariangela Torreglosa Ruiz; Eny Maria Goloni-Bertollo
Polymorphisms and haplotypes in methylenetetrahydrofolate reductase gene and head and neck squamous cell carcinoma risk.
Molecular biology reports 2012;39(1):635-43.
2011: Lidia Maria Rebolho Batista da Silva; Maysa Succi; Ana Lívia Silva Galbiatti; José Víctor Maniglia; Erika Cristina Pavarino-Bertelli; Luiz Sérgio Raposo; Mariangela Torreglosa Ruiz; Jéssika Nunes Gomes da Silva; Eny Maria Goloni-Bertollo
Head and neck carconogenesis: impact of MTHFD1 G1958A polymorphism.
Revista da Associação Médica Brasileira (1992) 2011;57(2):194-9.
2011: Ana Lívia Silva Galbiatti; Mariangela Torreglosa Ruiz; Daniela Rezende Pinto; Luiz Sérgio Raposo; José Victor Maníglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
A80G polymorphism of reduced folate carrier 1 (RFC1) gene and head and neck squamous cell carcinoma etiology in Brazilian population.
Molecular biology reports 2011;38(2):1071-8.
2010: Juliana Olsen Rodrigues; Ana Lívia Silva Galbiatti; Mariangela Torreglosa Ruiz; Luiz Sergio Raposo; José Victor Maniglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene and risk of head and neck squamous cell carcinoma.
Brazilian journal of otorhinolaryngology 2010;76(6):776-82.
2010: Ana L S Galbiatti; José V Maniglia; Erika Cristina Pavarino-Bertelli; Luis S Raposo; Mariangela T Ruiz; Eny Maria Goloni-Bertollo
The association between CBS 844ins68 polymorphism and head and neck squamous cell carcinoma risk - a case-control analysis.
Archives of medical science : AMS 2010;6(5):772-9.
2010: Cristiani Cortez Mendes; Joice Matos Biselli; Bruna Lancia Zampieri; Eny Maria Goloni-Bertollo; MN Eberlin; R Haddad; Maria Francesca Riccio; Helio Vannucchi; Valdemir Carvalho; Erika Cristina Pavarino-Bertelli
19-base pair deletion polymorphism of the dihydrofolate reductase (DHFR) gene: maternal risk of Down syndrome and folate metabolism.
São Paulo medical journal = Revista paulista de medicina 2010;128(4):215-8.
2010: Cássia Veridiana Dourado Leme; Luis Sérgio Raposo; Mariangela Torreglosa Ruiz; Joice Matos Biselli; Ana Lívia Silva Galbiatti; José Victor Maniglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
[GSTM1 and GSTT1 genes analysis in head and neck cancer patients].
Revista da Associação Médica Brasileira (1992) 2010;56(3):299-303.
2010: A L S Galbiatti; M T Ruiz; P M Biselli-Chicote; P M Chicote-Biselli; L S Raposo; J V Maniglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
5-Methyltetrahydrofolate-homocysteine methyltransferase gene polymorphism (MTR) and risk of head and neck cancer.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2010;43(5):445-50.
2010: Mariangela Torreglosa Ruiz; Janayna Fernanda Balachi; Raquel Aldrighi Fernandes; Ana Lívia Silva Galbiatti; José Victor Maniglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Analysis of the TAX1BP1 gene in head and neck cancer patients.
Brazilian journal of otorhinolaryngology 2010;76(2):193-8.
2010: M T Ruiz; Patrícia Matos Biselli; J V Maniglia; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Genetic variability of vascular endothelial growth factor and prognosis of head and neck cancer in a Brazilian population.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2010;43(2):127-33.
2010: Patrícia Matos Biselli; Alexandre Rodrigues Guerzoni; Moacir Fernandes de Godoy; MN Eberlin; R Haddad; Valdemir Carvalho; Helio Vannucchi; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease.
Journal of thrombosis and thrombolysis 2010;29(1):32-40.
2009: Erika Cristina Pavarino-Bertelli; Joice Matos Biselli; Daiana Bonfim; Eny Maria Goloni-Bertollo
Clinical profile of children with Down syndrome treated in a genetics outpatient service in the southeast of Brazil.
Revista da Associação Médica Brasileira (1992) 2009;55(5):547-52.
2009: Patrícia Matos Biselli; Alexandre Rodrigues Guerzoni; Eny Maria Goloni-Bertollo; Moacir Fernandes de Godoy; Juliana Aparecida Barcelos Abou-Chahla; Erika Cristina Pavarino-Bertelli
[MTHFR genetic variability on coronary artery disease development].
Revista da Associação Médica Brasileira (1992) 2009;55(3):274-8.
2009: Alexandre Rodrigues Guerzoni; Patrícia Matos Biselli; Moacir Fernandes de Godoy; Dorotéia Rossi Silva Souza; R Haddad; MN Eberlin; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Homocysteine and MTHFR and VEGF gene polymorphisms: impact on coronary artery disease.
Arquivos brasileiros de cardiologia 2009;92(4):263-8.
2009: Joice Matos Biselli; Filipe Brum Machado; B L Zampieri; A F Alves da Silva; Eny Maria Goloni-Bertollo; R Haddad; Marcos N Eberlin; Helio Vannucchi; Valdemir Carvalho; E Medina-Acosta; Erika Cristina Pavarino-Bertelli
Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
Genetic counseling (Geneva, Switzerland) 2009;20(3):225-34.
2008: Joice Matos Biselli; Daniela Brumati; Vivian Fernanda Frigeri; Bruna Lancia Zampieri; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli
A80G polymorphism of reduced folate carrier 1 (RFC1) and C776G polymorphism of transcobalamin 2 (TC2) genes in Down's syndrome etiology.
São Paulo medical journal = Revista paulista de medicina 2008;126(6):329-32.
2008: Geraldo Gaspar Paes Leme Coutinho; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli
Effectiveness of two programs of intermittent ferrous supplementation for treating iron-deficiency anemia in infants: randomized clinical trial.
São Paulo medical journal = Revista paulista de medicina 2008;126(6):314-8.
2008: Patrícia Matos Biselli; Alexandre Rodrigues Guerzoni; Moacir Fernandes de Godoy; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Vascular endothelial growth factor genetic variability and coronary artery disease in Brazilian population.
Heart and vessels 2008;23(6):371-5.
2008: Eny Maria Goloni-Bertollo; Mariangela Torreglosa Ruiz; Cristina B Vendrame Goloni; Marcos Pontes Muniz; Nelson Iguimar Valério; Erika Cristina Pavarino-Bertelli
GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
American journal of medical genetics. Part A 2008;146A(12):1523-9.
2008: Leonor Varela-Lema; Emanuela Taioli; Alberto Ruano-Ravina; Juan Miguel Barros-Dios; Devasena Anantharaman; Simone Benhamou; Stefania Boccia; Rajani A Bhisey; Gabriella Cadoni; Ettore Capoluongo; Chien-Jen Chen; William Foulkes; Eny Maria Goloni-Bertollo; Ana Hatagima; Richard Hayes; Takahiko Katoh; Sergio Koifman; Phillip Lazarus; Johannes J Manni; Manoj Mahimkar; Shunji Morita; Jong Park; Kwang-Kyun Park; Erika Cristina Pavarino-Bertelli; Enilze Maria de Souza Fonseca Ribeiro; Bidyut Roy; Margaret R Spitz; Richard C Strange; Qingyi Wei; Camille C Ragin
Meta-analysis and pooled analysis of GSTM1 and CYP1A1 polymorphisms and oral and pharyngeal cancers: a HuGE-GSEC review.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(6):369-84.
2008: Maria Paula Sanches de Alvarenga; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Comparing techniques for the identification of the MTHFR A1298C polymorphism.
Journal of biomolecular techniques : JBT 2008;19(2):103-5.
2008: José Roberto Lopes Ferraz Filho; Marcos Pontes Munis; Antonio Soares Souza; Rafael Angelo Sanches; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli
Unidentified bright objects on brain MRI in children as a diagnostic criterion for neurofibromatosis type 1.
Pediatric radiology 2008;38(3):305-10.
2008: Rosa Sayoko Kawasaki-Oyama; Domingo Braile; Heloisa Cristina Caldas; João Carlos Ferreira Leal; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli; Mário Abbud-Filho; Izaura Dos Santos
[Blood mesenchymal stem cell culture from the umbilical cord with and without Ficoll-Paque density gradient method].
Revista brasileira de cirurgia cardiovascular : órgão oficial da Sociedade Brasileira de Cirurgia Cardiovascular 2008;23(1):29-34.
2008: Joice Matos Biselli; Eny Maria Goloni-Bertollo; B L Zampieri; R Haddad; M N Eberlin; Erika Cristina Pavarino-Bertelli
Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: maternal risk factors for Down syndrome in Brazil.
Genetics and molecular research : GMR 2008;7(1):33-42.
2008: Joice Matos Biselli; Eny Maria Goloni-Bertollo; R Haddad; M N Eberlin; Erika Cristina Pavarino-Bertelli
The MTR A2756G polymorphism is associated with an increase of plasma homocysteine concentration in Brazilian individuals with Down syndrome.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2008;41(1):34-40.
2007: Patrícia Matos Biselli; M P Sanches de Alvarenga; Mário Abbud-Filho; M A S Ferreira-Baptista; A L S Galbiatti; M T Y Goto; M A Cardoso; MN Eberlin; R Haddad; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli
Effect of folate, vitamin B6, and vitamin B12 intake and MTHFR C677T polymorphism on homocysteine concentrations of renal transplant recipients.
Transplantation proceedings 2007;39(10):3163-5.
2007: M P S de Alvarenga; Erika Cristina Pavarino-Bertelli; Mário Abbud-Filho; M A S Ferreira-Baptista; R Haddad; MN Eberlin; Eny Maria Goloni-Bertollo
Combination of angiotensin-converting enzyme and methylenetetrahydrofolate reductase gene polymorphisms as determinant risk factors for chronic allograft dysfunction.
Transplantation proceedings 2007;39(1):78-80.
2006: Joice Matos Biselli; Renata Cristina de Angelo Calsaverini Leal; Mariângela Torreglosa Ruiz; Eny Maria Goloni-Bertollo; José Victor Maníglia; Andréa Regina Baptista Rossit; Erika Cristina Pavarino-Bertelli
GSTT1 and GSTM1 polymorphism in cigarette smokers with head and neck squamous cell carcinoma.
Brazilian journal of otorhinolaryngology 2006;72(5):654-8.
2006: Eny Maria Goloni-Bertollo; Joice Matos Biselli; Léa Carolina Delima Corrêa; José Victor Maníglia; Andréa Regina Baptista Rossit; Mariângela Torreglosa Ruiz; Erika Cristina Pavarino-Bertelli
[Evaluation of the influence of GSTT1 and GSTM1 null genotypes in head and neck carcinogenesis].
Revista da Associação Médica Brasileira (1992) 2006;52(5):365-8.
2006: Marcos R H Estécio; E M Youssef; Paula Rahal; Erica E Fukuyama; J F Góis-Filho; J V Maniglia; Eny Maria Goloni-Bertollo; Jean-Pierre J Issa; Eloiza H Tajara
LHX6 is a sensitive methylation marker in head and neck carcinomas.
Oncogene 2006;25(36):5018-26.
2006: Patrícia Matos Biselli; Mário Abbud-Filho; M A S Ferreira-Baptista; M P S de Alvarenga; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino-Bertelli
Angiotensin-converting enzyme gene polymorphism in chronic allograft nephropathy.
Transplantation proceedings 2006;38(5):1327-8.
2005: Alessandra B Trovó-Marqui; Eny Maria Goloni-Bertollo; N I Valério; Erika Cristina Pavarino-Bertelli; M P Muniz; M F Teixeira; J R Antonio; Eloiza H Tajara
High frequencies of plexiform neurofibromas, mental retardation, learning difficulties, and scoliosis in Brazilian patients with neurofibromatosis type 1.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2005;38(9):1441-7.
2005: Geraldo Gaspar Paes Leme Coutinho; Eny Maria Goloni-Bertollo; Erika Cristina Pavarino Bertelli
Iron deficiency anemia in children: a challenge for public health and for society.
São Paulo medical journal = Revista paulista de medicina 2005;123(2):88-92.
2004: Erika Cristina Pavarino-Bertelli; M P Sanches de Alvarenga; Eny Maria Goloni-Bertollo; M A S F Baptista; R Haddad; N F Hoerh; MN Eberlin; Mário Abbud-Filho
Hyperhomocysteinemia and MTHFR C677T and A1298C polymorphisms are associated with chronic allograft nephropathy in renal transplant recipients.
Transplantation proceedings 2004;36(10):2979-81.
2004: Alessandra B Trovó-Marqui; Eny Maria Goloni-Bertollo; Marta F Teixeira; Eloiza H Tajara
Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae.
Ophthalmic research 2004;36(6):349-52.
2004: Ana Carolina de Sá Viana; Raphael Roio Liberatore Junior; Eny Maria Goloni-Bertollo
[Puberty and growth in children and adolescents with neuro fibromatosis type 1].
Revista da Associação Médica Brasileira (1992) 2004;50(2):163-6.
2003: Eny Maria Goloni-Bertollo; Andréa Regina Baptista Rossit; João Batista Salomão Junior; Agnes Cristina Fett-Conte; Salmo Raskin
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from São Paulo State, Brazil.
Human biology 2003;75(3):393-8.
2002: Mário Abbud-Filho; Erika Cristina Pavarino-Bertelli; M P S Alvarenga; I M M Fernandes; R A Toledo; Eloiza H Tajara; M Savoldi-Barbosa; G H Goldmann; Eny Maria Goloni-Bertollo
Systemic lupus erythematosus and microchimerism in autoimmunity.
Transplantation proceedings 2002;34(7):2951-2.
2002: Ana Elizabete Silva; Sheila Adami Vayego-Lourenco; Agnes Cristina Fett-Conte; Eny Maria Goloni-Bertollo; Marileila Varella-Garcia
Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder.
Arquivos de neuro-psiquiatria 2002;60(2-A):290-4.