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Henrique Ferrer
Henrique Ferrer
Estudante de Medicina, Universidade Federal de São Paulo
Verified email at unifesp.br
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Cited by
Year
Correlation between GLA variants and alpha-Galactosidase A profile in dried blood spot: an observational study in Brazilian patients
P Varela, G Mastroianni Kirsztajn, FL Motta, RP Martin, LT Turaça, ...
Orphanet journal of rare diseases 15, 1-12, 2020
182020
Functional Characterization and Pharmacological Evaluation of a Novel GLA Missense Mutation Found in a Severely Affected Fabry Disease Family
P Varela, G Mastroianni Kirsztajn, H Ferrer, C Aranda, K Wallbach, ...
Nephron 144 (3), 147-155, 2020
112020
Identification of a novel GLA mutation in a family with classical phenotype of Fabry disease
HLF Ferrer, JB Pesquero, P Varela, C Aranda, AM Martins
Molecular Genetics and Metabolism 123 (2), S44-S45, 2018
2018
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Articles 1–3