| The specific impact of uremic toxins upon cognitive domains: a review ÁO Franco, RT Starosta, M Roriz-Cruz Brazilian Journal of Nephrology 41, 103-111, 2018 | 24 | 2018 |
| Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for … RT Starosta, S Boyer, S Tahata, K Raymond, HE Lee, LA Wolfe, C Lam, ... Orphanet Journal of Rare Diseases 16 (1), 1-12, 2021 | 22 | 2021 |
| Fetal glycosylation defect due to ALG3 and COG5 variants detected via amniocentesis: Complex glycosylation defect with embryonic lethal phenotype A Ferrer, RT Starosta, W Ranatunga, D Ungar, T Kozicz, E Klee, LM Rust, ... Molecular genetics and metabolism 131 (4), 424-429, 2020 | 12 | 2020 |
| Liver involvement in patients with Gaucher disease types I and III RT Starosta, FP e Vairo, AD Dornelles, SP Basgalupp, M Siebert, ... Molecular Genetics and Metabolism Reports 22, 100564, 2020 | 11 | 2020 |
| Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) initially diagnosed as ALG6-CDG: Functional evidence for benignity of the ALG6 c. 391T> C (p. Tyr131His) variant and … RT Starosta, J Tarnowski, FP e Vairo, K Raymond, G Preston, E Morava European Journal of Medical Genetics, 103941, 2020 | 7 | 2020 |
| Bone marrow burden score is not useful as a follow-up parameter in stable patients with type 1 Gaucher disease after 5 years of treatment LÁ Paskulin, RT Starosta, D Bertholdo, FP Vairo, L Vedolin, IVD Schwartz Blood Cells, Molecules, and Diseases 90, 102591, 2021 | 5 | 2021 |
| Elastic fibers density: a new parameter of improvement of NAFLD in bariatric surgery patients C Leite, RT Starosta, EN Trindade, E de Melo Monteiro, PF Pereira, ... Obesity Surgery 30 (10), 3839-3846, 2020 | 5 | 2020 |
| Hepatocellular carcinoma in Gaucher disease: Reinforcing the proposed guidelines. RT Starosta, FP Vairo, AD Dornelles, CTS Cerski, MR Álvares-da-Silva, ... Blood cells, molecules & diseases 74, 34, 2019 | 5 | 2019 |
| The frontal-subcortical syndrome RT Starosta, MV Vidor, M Roriz-Cruz Journal of Alzheimer's Disease & Parkinsonism. Califórnia. Vol. 6, no. 4 …, 2016 | 5 | 2016 |
| Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1 LA Paskulin, RT Starosta, VS Zizemer, S Basgalupp, D Bertholdo, ... Molecular Genetics and Metabolism Reports 21, 100544, 2019 | 4 | 2019 |
| DDOST‐CDG: Clinical and molecular characterization of a third patient with a milder and a predominantly movement disorder phenotype I Elsharkawi, P Wongkittichote, EJP Daniel, RT Starosta, K Ueda, BG Ng, ... Journal of Inherited Metabolic Disease 46 (1), 92-100, 2023 | 3 | 2023 |
| Misdiagnosis of Streptococcus gallolyticus endocarditis RT Starosta, R Rivero, FH de Oliveira, E Lopes, MR Cerski Autopsy & Case Reports 6 (3), 29, 2016 | 3 | 2016 |
| A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study MVMB Wilke, BM de Oliveira, RT Starosta, M Shinawi, L Lu, M He, Y Ma, ... Biomedicines 11 (2), 363, 2023 | 2 | 2023 |
| Corrected integrated density: a novel method for liver elastic fibers quantification in chronic hepatitis C C Leite, RT Starosta, EN Trindade, MRM Trindade, MR Álvares-da-Silva, ... Surgical and Experimental Pathology 3 (1), 1-7, 2020 | 2 | 2020 |
| Nuclear morphometry and chromatin texture changes in hepatocellular carcinoma samples may predict outcomes of liver transplanted patients JB Dos Santos, RT Starosta, EFS Pilar, JD Kunz, J Tomedi, CTS Cerski, ... BMC gastroenterology 22 (1), 1-9, 2022 | 1 | 2022 |
| Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations RT Starosta, YCC Hou, K Leestma, P Singh, L Viehl, L Manwaring, ... Frontiers in Pediatrics 10, 944178, 2022 | 1 | 2022 |
| Histomorphometric analysis of liver biopsies of treated patients with Gaucher disease type 1 RT Starosta, M Siebert, FP Vairo, BLL Costa, CT Ponzoni, IVD Schwartz, ... Autopsy and Case Reports 11, 2021 | 1 | 2021 |
| Nuclear Abnormalities in LMNA p.(Glu2Lys) Variant Segregating with LMNA-Associated Cardiocutaneous Progeria Syndrome MVMB Wilke, M Wick, TL Schwab, RT Starosta, KJ Clark, HM Connolly, ... Genes 15 (1), 112, 2024 | | 2024 |
| PIGO‐CDG: A case study with a new genotype, expansion of the phenotype, literature review, and nosological considerations RT Starosta, N Kerashvili, C Pruitt, MJ Schultz, SW Boyer, E Morava, ... JIMD reports 64 (6), 424-433, 2023 | | 2023 |
| Primary Mitochondrial Disorders in the Neonate RT Starosta, M Shinawi NeoReviews 23 (12), e796-e812, 2022 | | 2022 |
