| Early risks of death, stroke/systemic embolism, and major bleeding in patients with newly diagnosed atrial fibrillation: results from the GARFIELD-AF registry JP Bassand, S Virdone, SZ Goldhaber, AJ Camm, DA Fitzmaurice, ... Circulation 139 (6), 787-798, 2019 | 76 | 2019 |
| Effects of FTO RS9939906 and MC4R RS17782313 on obesity, type 2 diabetes mellitus and blood pressure in patients with hypertension A Marcadenti, FD Fuchs, U Matte, F Sperb, LB Moreira, SC Fuchs Cardiovascular diabetology 12, 1-8, 2013 | 71 | 2013 |
| Management and 1‐year outcomes of patients with newly diagnosed atrial fibrillation and chronic kidney disease: results from the prospective GARFIELD‐AF registry S Goto, P Angchaisuksiri, JP Bassand, AJ Camm, H Dominguez, ... Journal of the American Heart Association 8 (3), e010510, 2019 | 59 | 2019 |
| Mucolipidosis II and III alpha/beta in Brazil: analysis of the GNPTAB gene GK Cury, U Matte, O Artigalás, T Alegra, RV Velho, F Sperb, MG Burin, ... Gene 524 (1), 59-64, 2013 | 45 | 2013 |
| Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis F Sperb, F Vairo, M Burin, FQ Mayer, U Matte, R Giugliani Gene 512 (1), 113-116, 2013 | 39 | 2013 |
| Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databases GR Weber Hoss, F Sperb‐Ludwig, IVD Schwartz, HJ Blom Molecular Genetics & Genomic Medicine 8 (6), e1214, 2020 | 37 | 2020 |
| Analyses of disease-related GNPTABmutations define a novel GlcNAc-1-phosphotransferase interaction domain and an alternative site-1 protease cleavage site RV VELHO, R DE PACE, S KLUNDER, F Sperb-Ludwig, CM LOURENCO, ... | 33* | |
| Silver nanoparticle–ionic silsesquioxane: a new system proposed as an antibacterial agent AC Schneid, EW Roesch, F Sperb, U Matte, NP da Silveira, TMH Costa, ... Journal of Materials Chemistry B 2 (8), 1079-1086, 2014 | 32 | 2014 |
| Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients T Borsatto, F Sperb-Ludwig, SE Lima, MR S. Carvalho, PA S. Fonseca, ... PLoS One 12 (5), e0177503, 2017 | 31 | 2017 |
| Population analysis of the GLB1 gene in South Brazil C Baiotto, F Sperb, U Matte, CD Silva, R Sano, JC Coelho, R Giugliani Genetics and molecular biology 34, 45-48, 2011 | 29 | 2011 |
| CBS mutations are good predictors for B6‐responsiveness: A study based on the analysis of 35 Brazilian Classical Homocystinuria patients S Poloni, F Sperb‐Ludwig, T Borsatto, G Weber Hoss, MJR Doriqui, ... Molecular genetics & genomic medicine 6 (2), 160-170, 2018 | 27 | 2018 |
| Fabry disease: a new approach for the screening of females in high-risk groups G Pasqualim, L Simon, F Sperb-Ludwig, MG Burin, K Michelin-Tirelli, ... Clinical biochemistry 47 (7-8), 657-662, 2014 | 26 | 2014 |
| Biotinidase deficiency: clinical and genetic studies of 38 Brazilian patients T Borsatto, F Sperb-Ludwig, LLC Pinto, GR De Luca, FL Carvalho, ... BMC medical genetics 15, 1-7, 2014 | 24 | 2014 |
| Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry JPS Sawhney, VA Kothiwale, V Bisne, R Durgaprasad, P Jadhav, ... Indian heart journal 70 (6), 828-835, 2018 | 21 | 2018 |
| Determination of amylose/amylopectin ratio of starches T Nalin, F Sperb-Ludwig, K Venema, TGJ Derks, IVD Schwartz Journal of inherited metabolic disease 38, 985-986, 2015 | 20 | 2015 |
| Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease G Scaini, T Tonon, CF Moura de Souza, PF Schuck, GC Ferreira, ... Journal of Inherited Metabolic Disease 41, 631-640, 2018 | 19 | 2018 |
| Comparison of international normalized ratio audit parameters in patients enrolled in GARFIELD‐AF and treated with vitamin K antagonists DA Fitzmaurice, G Accetta, S Haas, G Kayani, H Lucas Luciardi, ... British journal of haematology 174 (4), 610-623, 2016 | 19 | 2016 |
| Enigmatic in vivo GlcNAc-1-phosphotransferase (GNPTG) transcript correction to wild type in two mucolipidosis III gamma siblings homozygous for nonsense mutations RV Velho, NF Ludwig, T Alegra, F Sperb-Ludwig, NR Guarany, U Matte, ... Journal of human genetics 61 (6), 555-560, 2016 | 18 | 2016 |
| Brain-derived neurotrophic factor expression increases after enzyme replacement therapy in Gaucher disease F Vairo, F Sperb-Ludwig, M Wilke, K Michellin-Tirelli, C Netto, EC Neto, ... Journal of neuroimmunology 278, 190-193, 2015 | 18 | 2015 |
| A de novo or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counseling RV Velho, T Alegra, F Sperb, NF Ludwig, ML Saraiva-Pereira, U Matte, ... Molecular Genetics and Metabolism Reports 1, 98-102, 2014 | 15 | 2014 |
