Browsing Comunicações em Eventos - FM/MPE by Issue Date

Browsing Comunicações em Eventos - FM/MPE by Issue Date

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  • BRAZ, L.; NICODEMO, A.; SOUZA, R.; SANTOS, N.; GODOY, N.; OKAY, T.; AMATO, V. (ELSEVIER SCI LTD, OXFORD, ENGLAND, 2012)
    Background: It is possible to perform the serological diagnosis of visceral leishmaniasis through k39 immunochromatographic test. However, usually in the co-infection visceral leishmaniasis with HIV k39 strip results are ...
  • ZAGO, C. A.; JACOB, C. M. A.; DINIZ, E. M. D. A.; ZERBINI, C.; DORNA, M.; FERNANDES, J.; ROCHA, V.; OLIVEIRA, J. B.; CARNEIRO-SAMPAIO, M. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Introduction: B+ SCID due to IL7Ra deficiency represents around 10% of SCID cases, and has seldom been described among Brazilian patients. Objective: We present two unrelated SCID female infants with IL7RA mutations and ...
  • ARANTES, J. M.; GRASSI, M. S.; SANTOS, N. M.; GUILHERME, L.; KULIKOWSKI, L. D.; DUTRA, R. L.; WATANABE, L. A.; JACOB, C. M. A.; ZAGO, C. A.; CARNEIRO-SAMPAIO, M. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Introduction: Chromosome 22q11 deletion is the most common human deletion and is found in the majority of patients with DiGeorge and velo-cardio-facial syndromes. Many patients have a mild to moderate immunodeficiency, and ...
  • LONGO-SANTOS, L. R.; TEODORO, W.; VELOSA, A. P.; MELLO, E.; PARRA, E.; COELHO, M. C.; ALVES, V.; CAPELOZZI, V.; TANNURI, U. (SPRINGER, NEW YORK, USA, 2012)
    Objective: Biliary atresia (BA) is the most common neonatal cholestatic disorder and the prime indication for liver transplantation (LTx) in children. Histopathological markers in liver biopsies emerge promise as indicator ...
  • DUARTE, R. J.; CRISTOFANI, L. M.; DENES, F. T.; GIRON, A. M.; ODONE-FILHO, V; SROUGI, M. (ELSEVIER SCIENCE BV, AMSTERDAM, NETHERLANDS, 2012)
    INTRODUCTION & OBJECTIVES: Modern image armamentarium allows the preoperative diagnosis of Wilms tumor and the use of preoperative chemotherapy as precluded by SIOP protocols without a biopsy specimen. However, misdiagnosis ...
  • SWENSSON, A.; CASTRO, A.; CASAGRANDE, R.; BITTENCOURT, T.; YONAMINE, G.; PASTORINO, A.; JACOB, C. (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background: Atopic dermatitis (AD) is a complex disease that can be or not related to atopy. The IgE levels and the presence of sensitisation has been associated to AD severity. The aim of this study is to evaluate the ...
  • BERGAMI-SANTOS, P. C.; CRISTOFANI, L.; ODONE-FILHO, V.; BARBUTO, J. A. (MARY ANN LIEBERT INC, NEW ROCHELLE, USA, 2012)
    Neuroblastoma is a common intra-abdominal tumor in children that may have an aggressive behavior and poor response to therapy, needing, therefore, new therapies. Monocyte-derived dendritic cells (Mo-DCs) can be applied in ...
  • WANG, X.; WAN, D.; JACOB, C.; FALCONE, F.; ALCOCER, M. (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background: Correlation between observed allergic clinical symptoms and specific IgE levels is poor in some cases. Current developments on basophil activation tests (BAT) are showing improved clinic relevance (compared to ...
  • HALLEY, Nathalia; CRISTOFANI, Lilian Maria; ALMEIDA, Maria Teresa Assis; MALUF-JUNIOR, Paulo Taufi; CORNACCHIONI, Ana Lucia Beltrati; TEIXEIRA, Roberto Augusto Plaza; ZAMPERLINI-NETO, Gabriele; GOMES, Alessandra Araujo; ODONE-FILHO, Vicente (WILEY PERIODICALS, INC, SAN FRANCISCO, USA, 2012)
    Purpose: Advanced neuroblastoma (stage 3 and 4) requires aggressive treatment, including surgery, chemo and radiotherapy and autologous bone marrow transplantation. Although long term survival rates are disappointing, those ...
  • BECK, C.; CASTRO, A.; GUSHKEN, A.; WATANABE, L.; BRANDAO, A.; YONAMINE, G.; PASTORINO, A.; JACOB, C. (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background: Food allergy affects about 6% of children and cow’s milk (CM) is the most important allergen. The majority of patients used to become tolerant during the first 3 years of life, but nowadays tolerance is being ...
  • ANDRADE, Luis Eduardo C.; PEREIRA, Kaline M. C.; FARIA, Atila G. A.; LIPHAUS, Bernadete; JESUS, Adriana A.; SILVA, Clovis; CARNEIRO-SAMPAIO, Magda (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background/Purpose: C4 is an important component of the Complement system and plays an essential role in the activation cascade of the classical Complement pathway. Complete C4 deficiency is among the strongest genetic ...
  • PERAZZIO, Sandro F.; SALOMAO, Reinaldo; SILVA, Neusa P.; CARNEIRO-SAMPAIO, Magda; ANDRADE, Luis Eduardo C. (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background/Purpose: Systemic Lupus Erythematosus (SLE) is known to be associated with deficiency of C1q, C4, and C2. There is high frequency of discoid lesions (2.7%) and SLE (0.5%) in Chronic Granulomatous Disease (CGD). ...
  • ALVAREZ, H. T.; SUZUKI, A. C. F.; TAKIUTI, J. H.; FERRIANI, M. P.; DORNA, M.; SANTOS, C.; PASTORINO, A. C.; CASTRO, A. P. B.; CARNEIRO-SAMPAIO, M.; JACOB, C. M. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Introduction: Primary immunodeficiencies (PID) are genetic diseases characterized by high susceptibility to infections. Although the manifestations affect all organs, there are few reports about ocular complications. ...
  • TORRES, L. C.; SOARES, D. C.; QUAIO, C. R. D. C.; FRANCO, J. F.; GOMY, I.; KULIKOWSKI, L. D.; BERTOLA, D. R.; SAMPAIO, M. Carneiro; KIM, C. A. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    The mucopolysaccharidoses (MPSs) are a group of rare diseases characterized by deficiencies in different enzymes required for degradation of complex carbohydrates. The enzymatic deficiencies lead to abnormal accumulation ...
  • TORRES, L. C.; QUAIO, C. R. D. C.; FRANCO, J. F.; GOMY, I.; BERTOLA, D. R.; KULIKOWSKI, L. D.; SAMPAIO, M. Carneiro; KIM, C. A. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Mucopolysaccharidoses (MPSs) are a group of inherited metabolic disorders characterized by the deficient activity of catabolic enzymes in the lysosomes and its consequent abnormal accumulation of deposits of glycosaminoglycans. ...
  • DEPNER, M.; WANDERS, J.; STAUSS, H.; JANSSON, A.; DUECKERS, G.; NIEHUES, T.; BAUMANN, U.; PEDERSEN, A. Stray; KILIC, S. S.; ATKINSON, T. P.; PUCK, J. M.; FRANCO, J. L.; DEVLIN, L.; JENSEN, T. D.; HENDERSON, P.; MATTHIJS, G.; SHOSHAN, M. Ben; MCCUSKER, C.; JACOB, C. M.; GRIMBACHER, B. (WILEY-BLACKWELL, HOBOKEN, USA, 2012)
    Background: Chronic mucocutaneous candidiasis (CMC) is characterized by recurrent or persistent infections of skin, nails or mucosa with candida species. Most of the cases are sporadic; however, both autosomal dominant and ...
  • JACOB, Cristina Miuki Abe; SANTOS, Cristiane de Jesus Nunes dos; SAINT-BASILE, Genevieve de; CASTRO, Ana Paula B. Moschione; PASTORINO, Antonio Carlos; FERNANDES, Juliana Folloni; ROCHA, Vanderson; CARNEIRO-SAMPAIO, Magda M. Sales (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Two female monozygotic twins presented: Case1-at2mo presented fever and vomiting after vaccination with DTP, Haemophilus, Salk, Rotavirus. The initial evaluation showed: anemia, hepatosplenomegaly, pancytopenia, LDH=0760 ...
  • FERREIRA, Leticia Bellinaso; DIAS, Diana Kimie; CASTRO, Ana Paula B. Moschione; PASTORINO, Antonio Carlos; DORNA, Mayra de Barros; ZAMPERLINI, Gustavo; CARNEIRO-SAMPAIO, Magda M. Sales; JACOB, Cristina Miuki Abe (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    A Brazilian boy with Ataxia-Telangiectasia (AT) diagnosed at 7 years of age, looked for the hospital at the age of 9 complaining of vomiting and disseminated hematomas for 10 days. The initial evaluation revealed only ...
  • DUARTE, R. J.; CRISTOFANI, L. M.; GIRON, A. M.; DENES, F. T.; ODONE-FILHO, V; TANNURI, U.; SROUGI, M. (ELSEVIER SCIENCE BV, AMSTERDAM, NETHERLANDS, 2012)
    INTRODUCTION & OBJECTIVES: Bilateral Wilms’ tumor represents 3% of all cases. The challenge of this situation is curing these patients preserving their renal function and quality of life (dialysis free status). Our purpose ...
  • DORNA, Mayra de Barros; CASTRO, Ana Paula B. Moschione; PASTORINO, Antonio Carlos; CARNEIRO-SAMPAIO, Magda M. Sales; JACOB, Cristina Miuki Abe (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Retrospective evaluation of 30 patients (21 M) aged 4.6–23.4 y (median 16.7 y) with predominantly humoral PID(9IDCV;14XLA;7HIGM).Mediantimeof follow-up9.2y(1.8–17.5). Median age of symptoms’ onset8mo(1–96 mo), age at ...

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