VANDERSON GERALDO ROCHA

(Fonte: Lattes)
Índice h a partir de 2011
22
Projetos de Pesquisa
Unidades Organizacionais
Departamento de Clínica Médica, Faculdade de Medicina - Docente
Instituto Central, Hospital das Clínicas, Faculdade de Medicina
LIM/31 - Laboratório de Genética e Hematologia Molecular, Hospital das Clínicas, Faculdade de Medicina - Líder

Resultados de Busca

Agora exibindo 1 - 8 de 8
  • bookPart
    Leucemias Crônicas
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • bookPart
    Síndrome Mielodisplásica (SMD)
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • bookPart
    Leucemias Agudas
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • bookPart
    Mieloma Múltiplo
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • bookPart
    Doença de Hodgkin
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • article 23 Citação(ões) na Scopus
    Autoimmune manifestations in SCID due to IL7R mutations: Omenn syndrome and cytopenias
    (2014) ZAGO, Claudia Augusta; JACOB, Cristina Miuki Abe; DINIZ, Edna Maria de Albuquerque; LOVISOLO, Silvana Maria; ZERBINI, Maria Claudia Nogueira; DORNA, Mayra; WATANABE, Leticia; FERNANDES, Juliana Folloni; ROCHA, Vanderson; OLIVEIRA, Joao Bosco; CARNEIRO-SAMPAIO, Magda
    B+NK+SCID (severe combined immunodeficiency) due to IL7R alpha deficiency represents approximately 10% of American SCID cases. To better understand the spectrum of autoimmune disorders associated with IL7R alpha deficiency, we describe two unrelated IL7R alpha-deficient female SCID infants whose clinical picture was dominated by autoimmune manifestations: one with intrauterine Omenn syndrome (OS) and another with persistent thrombocytopenic purpura since 4 months of age. The OS baby harbored a homozygous p.C118Y mutation in IL7R. She presented dense eosinophilic infiltrates in several organs, including pancarditis, which may have contributed to her death (on the 2nd day of life). B cells were observed in lymph nodes, spleen, bone marrow and thymus. The second patient harbored compound heterozygous p.01 8Y and p.I121NfsX8 mutations. She underwent a successful unrelated cord blood transplant. In conclusion, early OS can be observed in patients with IL7R mutations, and autoimmune cytopenias could also complicate the clinical course of SCID babies with this type of defect. (C) 2014 Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics.
  • bookPart
    Linfoma Não-Hodgkin
    (2014) NOVIS, Yana; ROCHA, Vanderson; RODRIGUES, Celso Arrais; FERREIRA, Fernando Blumm; FONSECA, Guilherme Hencklain; VILELA, Volney; TUCUNDUVA, Luciana
  • conferenceObject
    Hemophagocytic Syndrome Due to Perforin-Deficiency in Three Brazilian Infants: Immunization Could be the Trigger?
    (2014) JACOB, Cristina Miuki Abe; SANTOS, Cristiane de Jesus Nunes dos; GOMES, Monizi Campelo; PASTORINO, Antonio Carlos; DORNA, Mayra de Barros; FERNANDES, Juliana Folloni; CASTRO, Ana Paula B. Moschione; ROCHA, Vanderson; HAMERSCHLAK, Nelson; SAINT-BASILE, Genevieve de; CARNEIRO-SAMPAIO, Magda M. Sales