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Fernanda Bender

Observed names: Bender Fernanda, Bender, Fernanda, F. Bender, Fernanda B. Pasetto, Fernanda Bender Pasetto, Fernanda Bender-Pasetto, Fernanda H. Bitencourt, Fernanda Hendges de Bitencourt
ORCID: 0000-0003-3169-9291
Observed ORCID: 0000-0003-3169-9291
OpenAlex ID: A5022970629
Oxidative stress and inflammation in mucopolysaccharidosis type IVA patients treated with enzyme replacement therapy
2015 · Bruna Donida, Desirèe P. Marchetti, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 71
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Genetic studies in a cluster of Mucopolysaccharidosis Type VI patients in Northeast Brazil
2011 · Fabiana Moura Costa-Motta, Angelina Xavier Acosta, et al. · Molecular Genetics and Metabolism · 42
Oxidative and nitrative stress and pro-inflammatory cytokines in Mucopolysaccharidosis type II patients: effect of long-term enzyme replacement therapy and relation with glycosaminoglycan accumulation
2016 · Carlos Eduardo Diaz Jacques, Bruna Donida, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 38
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Investigation of newborns with abnormal results in a newborn screening program for four lysosomal storage diseases in Brazil
2017 · Heydy Bravo, Eurico Camargo Neto, et al. · Molecular Genetics and Metabolism Reports · 37
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A Community-Based Study of Mucopolysaccharidosis Type VI in Brazil: The Influence of Founder Effect, Endogamy and Consanguinity
2014 · Fabiana Moura Costa-Motta, Fernanda Bender, et al. · Human Heredity · 36
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Updated birth prevalence and relative frequency of mucopolysaccharidoses across Brazilian regions
2021 · Juliana Alves Josahkian, Franciele Barbosa Trapp, et al. · Genetics and Molecular Biology · 26
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Elevation of glycosaminoglycans in the amniotic fluid of a fetus with mucopolysaccharidosis VII: Prenatal diagnosis of an MPS VII fetus
2017 · Francyne Kubaski, Ana Carolina Brusius-Facchin, et al. · Prenatal Diagnosis · 21
Neonatal screening for spinal muscular atrophy: A pilot study in Brazil
2023 · Alice Brinckmann Oliveira Netto, Ana Carolina Brusius-Facchin, et al. · Genetics and Molecular Biology · 19
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Reliable detection of mucopolysacchariduria in dried-urine filter paper samples
2012 · G. Civallero, F. Bender, et al. · Clinica Chimica Acta · 19
Population medical genetics: translating science to the community
2019 · Roberto Giugliani, Fernanda Bender, et al. · Genetics and Molecular Biology · 14
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Newborn screening for lysosomal disorders in Brazil: A pilot study using customized fluorimetric assays
2020 · Fernanda Bender, Maira G. Burin, et al. · Genetics and Molecular Biology · 11
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Medical Costs Related to Enzyme Replacement Therapy for Mucopolysaccharidosis Types I, II, and VI in Brazil: A Multicenter Study
2015 · Fernanda Hendges de Bitencourt, Taiane Alves Vieira, et al. · Value in Health Regional Issues · 9
Screening for Attenuated Forms of Mucopolysaccharidoses in Patients with Osteoarticular Problems of Unknown Etiology
2015 · Thabata Caroline da Rocha Siqueira, Carolina Fischinger Moura de Souza, et al. · JIMD Reports · 9
Follow-up of pre-motor symptoms of Parkinson’s disease in adult patients with Gaucher disease type 1 and analysis of their lysosomal enzyme profiles in the CSF
2023 · Matheus Vernet Machado Bressan Wilke, Fabiano Poswar, et al. · Orphanet Journal of Rare Diseases · 4
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Clinical and genetic features of Classic Galactosemia in the south of Brazil
2025 · Leonardo Simão Medeiros, Lucas Ferreira Teixeira, et al. · Molecular Genetics and Metabolism · 3
COVID-19 impact on the diagnosis of Inborn Errors of Metabolism: Data from a reference center in Brazil
2021 · Fernanda Medeiros Sebastião, Kristiane Michelin-Tirelli, et al. · Genetics and Molecular Biology · 3
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Diagnostic networks for IEM in Brazil: report on 10 years of activity of the LSD Brazil Network, helping Brazil and Latin America to identify patients with lysosomal storage diseases
2025 · Franciele Barbosa Trapp, Mariluce Riegel, et al. · Journal of Community Genetics · 2
Medium-chain acyl-CoA dehydrogenase deficiency: prevalence of ACADM pathogenic variants c.985A>G and c.199T>C in a healthy population in Rio Grande do Sul, Brazil
2022 · Mariana Lopes dos Santos, Dévora Natalia Randon, et al. · Reproductive and Developmental Medicine · 2
MPS I and MPS II: Minimal estimated incidence in Brazil and comparison to the rest of the world
2015 · Andressa Federhen, Carla de Cássia Cascaes Batista, et al. · Molecular Genetics and Metabolism · 2
A Brazilian patient with late infantile metachromatic leukodystrophy treated with lentiviral hematopoietic stem-cell gene therapy: A report from prenatal diagnosis to early treatment
2023 · Larissa Faqueti, Gabrielle Iop, et al. · Molecular Genetics and Metabolism · 1
Enzyme Replacement Therapy With Elosulfase Alfa Decreases Storage of Glycosaminoglycan in White Blood Cells of Patients With Morquio A Syndrome
2015 · Guilherme Baldo, Fabiano Poswar, et al. · Journal of Inborn Errors of Metabolism and Screening · 1
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Analysis of C6S/C4S ratio in Morquio syndrome type A patients
2015 · Francyne Kubaski, Tsutomu Shimada, et al. · Molecular Genetics and Metabolism · 1
Contents Vol. 77, 2014
2014 · Joël Zlotogora, Stavit A. Shalev, et al. · Human Heredity · 1
Newborn Screening for MPS VI in a High-incidence Area of Northeast Brazil: Preliminary Results of a Pilot Program
2012 · Roberto Giugliani, Fernanda Bender, et al. · Molecular Genetics and Metabolism · 1
Triagem neonatal para mucopolissacaridose tipo VI (Síndrome de Maroteux-Lamy) em uma região com alta incidência da doença
2011 · Fernanda Bender · Americanae (AECID Library) · 1
Works count: 62
Citation count: 374
H-index: 11
I10-index: 11
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