Bone marrow failure

by Rodrigo T. Calado
Published 2020-10-01

Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child

by Cresio Alves, Julia Constanca Fernandes, Silvana Sampaio, Raquel de Melo Alves Paiva, Rodrigo Tocantins Calado
Published 2013-01-01

Direct comparison of flow-FISH and qPCR as diagnostic tests for telomere length measurement in humans.

by Fernanda Gutierrez-Rodrigues, Bárbara A Santana-Lemos, Priscila S Scheucher, Raquel M Alves-Paiva, Rodrigo T Calado
Published 2014-01-01

Ex vivo evaluation of intravitreal mesenchymal stromal cell viability using bioluminescence imaging

by Carolina Assis P. Vilela, Lucas Eduardo B. Souza, Rubens C. Siqueira, Rodrigo T. Calado, Dimas T. Covas, Jayter S. Paula
Published 2018-06-01

Telomere length correlates with disease severity and inflammation in sickle cell disease

by Marina Pereira Colella, Barbara A. Santana, Nicola Conran, Vinicius Tomazini, Fernando F. Costa, Rodrigo T. Calado, Sara T. Olalla Saad

BCL2A1a over-expression in murine hematopoietic stem and progenitor cells decreases apoptosis and results in hematopoietic transformation.

by Jean-Yves Métais, Thomas Winkler, Julia T Geyer, Rodrigo T Calado, Peter D Aplan, Michael A Eckhaus, Cynthia E Dunbar
Published 2012-01-01

Splicing factor SF3B1 mutations and ring sideroblasts in myelodysplastic syndromes: a Brazilian cohort screening study

by Flávia Sacilotto Donaires, Felipe Martelli, Raquel de Melo Alves-Paiva, Silvia Maria Meira Magalhães, Ronald Feitosa Pinheiro, Rodrigo Tocantins Calado

Familial pulmonary fibrosis: a heterogeneous spectrum of presentations

by Ana Beatriz Hortense, Marcel Koenigkam dos Santos, Danilo Wada, Alexandre Todorovic Fabro, Mariana Lima, Silvia Rodrigues, Rodrigo Tocantins Calado, José Baddini-Martinez

THPO gene variants in patients with acquired aplastic anemia

by Pedro Henrique Padilha, Gustavo Borges, Barbara Amélia Santana, Larissa Alessandra Medeiros, Samir Kanaan Nabhan, Ricardo Pasquini, Flavia Sacilotto Donaires, Rodrigo Tocantins Calado
Published 2018-10-01

A spectrum of severe familial liver disorders associate with telomerase mutations.

by Rodrigo T Calado, Joshua A Regal, David E Kleiner, David S Schrump, Nathan R Peterson, Veronica Pons, Stephen J Chanock, Peter M Lansdorp, Neal S Young
Published 2009-11-01

Efficacy of COVID-19 outbreak management in a skilled nursing facility based on serial testing for early detection and control

by Pedro M.M. Garibaldi, Natasha N. Ferreira, Glenda R. Moraes, José C. Moura, Danillo L.A. Espósito, Gustavo J. Volpe, Rodrigo T. Calado, Benedito A.L. Fonseca, Marcos C. Borges
Published 2021-03-01

Telomere biology and telomerase mutations in cirrhotic patients with hepatocellular carcinoma.

by Flávia S Donaires, Natália F Scatena, Raquel M Alves-Paiva, Joshua D Podlevsky, Dhenugen Logeswaran, Barbara A Santana, Andreza C Teixeira, Julian J-L Chen, Rodrigo T Calado, Ana L C Martinelli
Published 2017-01-01

Is the telomere length associated with neurocognitive disabilities in HIV-1-infected subjects?

by Marilia Ladeira de Araújo, Wellington Duarte, Augusto César Penalva de Oliveira, Maria Rita Polo Gascón, Luiz Augusto Marcondes Fonseca, Raquel de Melo Alves Paiva, Bárbara Santana, Rodrigo Tocantins Calado, Jorge Casseb
Published 2018-04-01

Telomere dynamics and hematopoietic differentiation of human DKC1-mutant induced pluripotent stem cells

by Flavia S. Donaires, Raquel M. Alves-Paiva, Fernanda Gutierrez-Rodrigues, Fernanda Borges da Silva, Maria Florencia Tellechea, Lilian Figueiredo Moreira, Barbara A. Santana, Fabiola Traina, Cynthia E. Dunbar, Thomas Winkler, Rodrigo T. Calado
Published 2019-10-01

Anti-complement Treatment for Paroxysmal Nocturnal Hemoglobinuria: Time for Proximal Complement Inhibition? A Position Paper From the SAAWP of the EBMT

by Antonio M. Risitano, Antonio M. Risitano, Serena Marotta, Serena Marotta, Patrizia Ricci, Luana Marano, Camilla Frieri, Fabiana Cacace, Michela Sica, Austin Kulasekararaj, Austin Kulasekararaj, Rodrigo T. Calado, Phillip Scheinberg, Rosario Notaro, Regis Peffault de Latour, Regis Peffault de Latour
Published 2019-06-01

GATA2 mutation in long stand Mycobacterium kansasii infection, myelodysplasia and MonoMAC syndrome: a case-report

by Daniela Palheiro Mendes-de-Almeida, Francianne Gomes Andrade, Gustavo Borges, Filipe V. dos Santos-Bueno, Iracema F. Vieira, Luana Kelly M. da S. da Rocha, Daniella A. Mendes-da-Cruz, Rosely M. Zancopé-Oliveira, Rodrigo T. Calado, Maria S. Pombo-de-Oliveira
Published 2019-04-01