Browsing Comunicações em Eventos - LIM/56 by Issue Date

Browsing Comunicações em Eventos - LIM/56 by Issue Date

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  • BATISTA, V. G.; TOLEDO, M. S.; STRAUS, A. H.; TAKAHASHI, H. K.; VASCONCELOS, D. Moraes; DUARTE, A. J.; BENARD, G. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Paracoccidioidomycosis (PCM) is the most important systemic mycosis in Latin America. As in other endemic infectious diseases, only a minority of the exposed individuals will develop the disease; however, the mechanisms ...
  • ALMEIDA, Lais Pinto de; LEITE, Olavo Henrique Munhoz; NICODEMO, Antonio Carlos; ORII, Noemia Mie; DIAS, Alana dos Santos; MORAES-VASCONCELOS, Dewton de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    HLA class I deficiency is a rare immunodeficiency characterized by recurrent respiratory infections and skin ulcers with granuloma. Herein we describe two patients with HLA class I deficiency with skin lesions and sinopulmonary ...
  • MORAES-VASCONCELOS, D.; PAGGIARO, A. O.; ISAAC, C.; RIBEIRO, R. L.; NICODEMO, A. C. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Human leukocyte antigen class I (HLA-I) deficiency is a rare disease (less than 30 reported cases in the world) with remarkable clinical and biological heterogeneity. It presents a 90-99% reduction reduction in the expression ...
  • ALMEIDA, L. P.; KHOURY, Z.; SZESZS, M. W.; BEZERRA, T. Almeida; ORII, N. M.; MORAES-VASCONCELOS, D. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    The host immune response to C. neoformans infection is the result of a complex interplay between cellular and humoral immunity that often guarantees the control of infection in the immunocompetent host. Mendelian susceptibility ...
  • SILVA, E. G.; SOARES, Maria Cecilia Pereira; MORAES-VASCONCELOS, Dewton de; DIAS, A. L. T.; CHANG, M. R.; RUIZ, L. S.; GAMBALE, Valderez; PRATES, R. A.; RIBEIRO, M. S.; PAULA, Claudete Rodrigues de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    The model of systemic cryptococcosis in BALB/c SCID mice is useful for immunological and therapeutic study of the disease in immunodeficient hosts. They are susceptible to experimental cryptococcosis by C. neoformans var. ...
  • ORFALI, Raquel Lean; RIVITTI, Evandro; SATO, Maria Notomi; TAKAOKA, Roberto; AOKI, Valeria (MOSBY-ELSEVIER, NEW YORK, USA, 2012)
    Objective: Evaluation of interleukins (IL) 17, 22, and 23 induced by Staphylococcus aureus enterotoxin stimulation in peripheral blood mononuclear cells (PBMC) of adults with atopic dermatitis. Background: Atopic dermatitis ...
  • LOUREIRO, Vivian Barzi; MARUTA, Celina; SANTI, Claudia Giuli; AOKI, Valeria (MOSBY-ELSEVIER, NEW YORK, USA, 2012)
    Background: Pemphigus is a rare autoimunne bullous disease, characterized by blisters and erosions of the skin and/or mucous membranes. Its potentially life-threatening condition has been modified after the introduction ...
  • HIRAYAMA, Andre; MARUTA, Celina; SANTI, Claudia; AOKI, Valeria (MOSBY-ELSEVIER, NEW YORK, USA, 2012)
    Background: Lichen planus pemphigoides (LPP) is a rare autoimmune subepidermal blistering disease that shares clinical and/or immunopathologic features of lichen planus (LP) and bullous pemphigoid (BP). Epitope-spreading ...
  • GRUMACH, Anete Sevciovic; BARROS, Noac Chuffi; DOMINGUES-FERREIRA, Mauricio; ALMEIDA, Lais Pinto de; BEZERRA, Thiago de Almeida; LEVY, Ariel; MADALENA, Cintia Vargas; DUARTE, Alberto Jose da Silva; MORAES-VASCONCELOS, Dewton de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Hereditary angioedema (HAE) is characterized by deficiency of the C1 esterase inhibitor. This protein controls the activation of complement and also the process of coagulation, fibrinolysis, and bradykinin pathway. It is ...
  • SOARES, Maria Cecilia Pereira; COLLANIERI, Anna Cristina; YASUHARA, Fabiana; DUARTE, Alberto Jose da Silva; MORAES-VASCONCELOS, Dewton de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Common variable immunodeficiency (CVID) is a humoral immunodeficiency. Recently the discovery of genes related to the cause of CVID has been reported, among them ICOS. ICOS is a co-stimulatory molecule expressed in T cells ...
  • BEZERRA, Thiago de Almeida; ALMEIDA, Lais Pinto de; PEREIRA, Juliana; DUARTE, Alberto Jose da Silva; MORAES-VASCONCELOS, Dewton de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Angioedema due to acquired C1-inhibitor deficiency is a rare, life-threatening disease with poorly defined etiology, therapy, and prognosis. It is characterized by increase in vascular permeability (angioedema) of the skin, ...
  • COLLANIERI, Anna Cristina; SOARES, Maria Cecilia Pereira; ALMEIDA, Lais Pinto de; BEZERRA, Thiago de Almeida; DUARTE, Alberto Jose da Silva; MORAES-VASCONCELOS, Dewton de (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Common variable immunodeficiency (CVID) is a humoral immunodeficiency. In recent years, the discovery of related genes has broadened, including TACI, ICOS, CD19, CD20, CD81 and BAFF-R. We selected 20 CVID patients and 20 ...
  • NALI, L. H. S.; SUMITA, L. M.; FINK, M. C. D.; OLIVAL, G. S.; SANTIAGO, T. F.; V, J. E. Bermudez; MORAES, L.; CAVENAGHI, V; TILBERY, C. P.; CALLEGARO, D.; CASSEB, J. S.; PENALVA-DE-OLIVEIRA, A. C.; ROMANO, C. M. (SAGE PUBLICATIONS LTD, LONDON, ENGLAND, 2012)
  • MORAES-VASCONCELOS, D.; RIGATO, P. O.; DIAS, A. Santos; ALVES, C.; ORII, N. M.; OGUSUKU, S.; FERREIRA, M. Domingues (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Primary immunodeficiencies are rare and usually first manifest during childhood. Invasive aspergillosis is the leading cause of mortality in phagocyte defects, reflecting the key role of these cells in the host defense ...
  • MORAES-VASCONCELOS, D.; ORII, N. M.; DIAS, A. Santos; BEZERRA, T. Almeida; CAMPEAS, A.; LIAN, Y. C.; BRASIL, R. A. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Mendelian inheritance to mycobacterial disease (MSMD) refers to a group of diseases characterized by predisposition to clinical disease caused by environmental non-tuberculous or poorly virulent mycobacterial species such ...
  • RAMALHO, V. D.; VASCONCELOS, D.; ROXO, P.; SILVA, M. T. N. da; VILELA, M. M. S. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    Background: X-linked agammaglobulinemia (XLA) is a humoral primary immunodeficiency in which affected patients have very low levels of peripheral B cells and a profound deficiency of all immunoglobulin isotypes. The ...
  • CENTEVILLE, M.; VANESSA, R. D.; ABRAMCZUK, B. M.; MAZZOLA, T. N.; VASCONCELOS, D. M.; ROXO, P.; SILVA, M. T. N. da; VILELA, M. M. S. (SPRINGER/PLENUM PUBLISHERS, NEW YORK, USA, 2012)
    The aim of this study was to investigate whether X- Linked Agammaglobulinaemia (XLA) patients with BCG scars can alter the subset composition, activation or function of specific BCG T cells and pro and anti inflammatory ...
  • THOMAZ, R. B.; OLIVAL, G. S.; TILBERY, C. P.; BERMUDEZ, J. V.; NALI, L. H. S.; ROMANO, C. M.; MORAES, L.; CALLEGARO, D.; CAVENAGHI, V.; CASSEB, J. S.; OLIVEIRA, A. C. Penalva de; FINK, C.; SUMITA, L. S. (SAGE PUBLICATIONS LTD, LONDON, ENGLAND, 2012)
  • ORFALI, R. L.; SATO, M. N.; SANTOS, V. G. Dos; TITZ, T. O.; DUARTE, A. S.; TAKAOKA, R.; AOKI, V. (NATURE PUBLISHING GROUP, NEW YORK, USA, 2013)
    The aim of this study was to evaluate the profile of anti-Staphylococcus aureus enterotoxin B (SEB) antibody (Ab) response in adults with AD. We selected 38 patients diagnosed as AD (Hanifin & Rajka's criteria), aged between ...
  • DELGADO, Livia; MARUTA, Celina W.; SANTI, Claudia G.; MYAMOTO, Denise; AOKI, Valeria (MOSBY-ELSEVIER, NEW YORK, USA, 2013)
    Background: Pemphigus is a rare autoimmune blistering dermatosis. The shift from a disease to another is known as ‘‘epitope spreading’’ (ES). A primary inflammatory/autoimmune process releases ‘‘hidden’’ epitopes, and ...

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