Maria Odete Esteves Hilário

ORCID: 0000-0003-4867-789X
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About
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Research Areas
  • Autoimmune and Inflammatory Disorders Research
  • Systemic Lupus Erythematosus Research
  • Adolescent and Pediatric Healthcare
  • Inflammatory Myopathies and Dermatomyositis
  • Childhood Cancer Survivors' Quality of Life
  • Renal Diseases and Glomerulopathies
  • Vasculitis and related conditions
  • Streptococcal Infections and Treatments
  • Immunodeficiency and Autoimmune Disorders
  • Inflammasome and immune disorders
  • Rheumatoid Arthritis Research and Therapies
  • Systemic Sclerosis and Related Diseases
  • Dermatological and Skeletal Disorders
  • Ocular Diseases and Behçet’s Syndrome
  • Hematological disorders and diagnostics
  • Eosinophilic Disorders and Syndromes
  • Bone health and treatments
  • Musculoskeletal Disorders and Rehabilitation
  • Hemoglobinopathies and Related Disorders
  • Acute Lymphoblastic Leukemia research
  • Chronic Lymphocytic Leukemia Research
  • Spondyloarthritis Studies and Treatments
  • Eosinophilic Esophagitis
  • Otitis Media and Relapsing Polychondritis
  • Whipple's Disease and Interleukins

Universidade Federal de Ciências da Saúde de Porto Alegre
2019-2021

Rafael Advanced Defense Systems (Israel)
2019

Universidade Federal de São Paulo
2008-2018

Santa Casa de Misericórdia de Marília
2017

Irmandade da Santa Casa de Misericórdia de São Paulo
2017

Fundação de Apoio à Universidade Federal de São Paulo
2003-2013

Universidade de São Paulo
2004-2009

Charles University
2004

Hospital Universitario La Paz
2004

Cornell University
2004

<h3>Objectives</h3> To validate the previously proposed classification criteria for Henoch–Schönlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA). <h3>Methods</h3> Step 1: retrospective/prospective web-data collection children with HSP, c-PAN, c-WG c-TA age at diagnosis ≤18 years. 2: blinded by consensus panel of a representative sample 280 cases. 3: statistical (sensitivity, specificity, area under curve κ-agreement)...

10.1136/ard.2009.116657 article EN Annals of the Rheumatic Diseases 2010-04-22

Objective. Juvenile localized scleroderma (JLS) includes a number of conditions often grouped together. With the long-term goal developing uniform classification criteria, we studied epidemiological, clinical and immunological features children with JLS followed by paediatric rheumatology dermatology centres.

10.1093/rheumatology/kei251 article EN Lara D. Veeken 2005-12-20

OBJETIVOS: Avaliar a confiabilidade e validade da versão brasileira do questionário genérico Pediatric Quality of Life InventoryTM (PedsQL TM 4.0) mensurar qualidade de vida crianças adolescentes saudáveis pacientes com doenças reumáticas. MÉTODOS: No processo validação, seguimos metodologia proposta pelos idealizadores original em inglês PedsQL 4.0. O instrumento foi administrado por entrevista dois grupos: 240 aparentemente São Paulo (SP) 105 reumáticas crônicas, pareados idade, aos...

10.1590/s0021-75572008000400005 article PT Jornal de Pediatria 2008-08-01
Michael J. Ombrello Elaine F. Remmers Ioanna Tachmazidou Alexei A. Grom Dirk Foell and 95 more Johannes‐Peter Haas Alberto Martini Marco Gattorno Seza Özen Sampath Prahalad Andrew Zeft John F. Bohnsack Elizabeth Mellins Norman T. Ilowite Ricardo Russo Cláudio Arnaldo Len Maria Odete Esteves Hilário Sheila Oliveira Rae S. M. Yeung Alan Rosenberg Lucy R. Wedderburn Jordi Antón Tobias Schwarz Anne Hinks Yelda Bilginer Jane Park Joanna Cobb Colleen Satorius Buhm Han Elizabeth Baskin Sara Signa Richard H. Duerr J ACHKAR M. Ilyas Kamboh Kenneth M. Kaufman Leah C. Kottyan Dalila Pinto Stephen W. Scherer Marta E. Alarcón‐Riquelme Elisa Docampo Xavier Estivill Ahmet Gül Paul I. W. de Bakker Soumya Raychaudhuri Carl D. Langefeld Susan D. Thompson Eleftheria Zeggini Wendy Thomson Daniel L. Kastner Patricia Woo J ACHKAR Marta E. Alarcón‐Riquelme Roger C. Allen Jordi Antón Elizabeth Baskin Stefan Berg Bianca Bica Yelda Bilginer John F. Bohnsack André Cavalcanti Jeffrey Chaitow Joanna Cobb Rubin Cuttica Paul I. W. de Bakker Elisa Docampo Richard H. Duerr Justine A. Ellis Xavier Estivill Terri H. Finkel Dirk Foell Marco Gattorno Alexei A. Grom Ahmet Gül Johannes‐Peter Haas Hákon Hákonarson Buhm Han Maria Odete Esteves Hilário Anne Hinks Norman T. Ilowite M. Ilyas Kamboh Daniel L. Kastner Kenneth M. Kaufman Leah C. Kottyan Carl Langefeld Cláudio Arnaldo Len Alberto Martini Elizabeth Mellins Kirstin Minden Kevin Murray Sheila Knupp Feitosa de Oliveira Michael J. Ombrello Seza Özen Jane Park Dalila Pinto Sampath Prahalad Pierre Quartier Soumya Raychaudhuri Elaine F. Remmers Alan Rosenberg Ricardo Russo

Systemic juvenile idiopathic arthritis (sJIA) is an often severe, potentially life-threatening childhood inflammatory disease, the pathophysiology of which poorly understood. To determine whether genetic variation within MHC locus on chromosome 6 influences sJIA susceptibility, we performed association study 982 children with and 8,010 healthy control subjects from nine countries. Using meta-analysis directly observed imputed SNP genotypes classic HLA types, identified as a bona fide...

10.1073/pnas.1520779112 article EN Proceedings of the National Academy of Sciences 2015-11-23

Objectives Juvenile idiopathic arthritis (JIA) is a heterogeneous group of conditions unified by the presence chronic childhood without an identifiable cause. Systemic JIA (sJIA) rare form characterised systemic inflammation. sJIA distinguished from other forms unique clinical features and treatment responses that are similar to autoinflammatory diseases. However, approximately half children with develop destructive, long-standing appears JIA. Using genomic approaches, we sought gain novel...

10.1136/annrheumdis-2016-210324 article EN cc-by-nc Annals of the Rheumatic Diseases 2016-12-07

CONTEXTO: A autopercepção e a satisfação com imagem corporal são fatores preponderantes na auto-aceitação do adolescente podem gerar atitudes inadequadas que prejudicam seu crescimento desenvolvimento. OBJETIVO: Relacionar o estado nutricional percepção da tem de si próprio. MÉTODOS: informação índice massa (IMC) foi obtida por dados antropométricos para classificar nutricional. Utilizaram-se silhuetas padronizadas avaliar um questionário autopreenchimento determinar corporal. RESULTADOS:...

10.1590/s0101-60832006000600001 article PT Archives of Clinical Psychiatry (São Paulo) 2006-01-01

Sera from 214 healthy children and adolescents (108 females [50.4%]) aged 6 months to 20 years (mean 8.7 years) 116 patients with rheumatic diseases were assayed for antinuclear antibody (ANA) by indirect immunofluorescence (IIF) using HEp-2 cells as substrate. Twenty-seven (12.6%) presented a positive ANA test; there was no difference between genders, we observed trend higher frequency of ≥1/80 among 5 10 years. Eight the 27 test reevaluated 36 later, none them had developed any disease,...

10.1177/000992280404300709 article EN Clinical Pediatrics 2004-09-01

To evaluate the quality of life in children and adolescents with sickle cell disease attending a blood reference center, to assess their relatives.Cross-sectional study that included 100 patients disease, which were divided into three subgroups according age: 5 7 (n=18), 8 12 (n=32), 13 18 years-old (n=50), parents. The Control Group 50 healthy from public local school, also same age caregivers. Pediatric Quality Inventory (PedsQL), version 4.0, was applied both groups. generic questionnaire...

10.1590/s0103-05822013000100005 article EN cc-by Revista Paulista de Pediatria 2013-03-01

Musculoskeletal complaints may be associated with neoplasias as an initial manifestation of the disease. When these symptoms predominate at onset disease, differential diagnosis includes several rheumatic diseases.To assess frequency, clinical features and types cancer manifested in children presenting musculoskeletal over a seven-year period.Retrospective.Discipline Allergy, Clinical Immunology Rheumatology, Universidade Federal de São Paulo-Escola Paulista Medicina.The medical records...

10.1590/s1516-31802005000100005 article EN cc-by Sao Paulo Medical Journal 2005-01-01

We evaluated the prevalence and clinical associations of amenorrhea in 298 female juvenile systemic lupus erythematosus (JSLE) patients (ACR criteria) followed 12 Brazilian Paediatric Rheumatology centres. Amenorrhea was observed 35 (11.7%) with a mean duration 7.2 ± 3.6 months. The hormones were performed 32/35 none them had FSH LH levels above estradiol below normal range according to pubertal changes. JSLE younger (15.04 2.5 versus 17.8 3.1 years; P = 0.001), shorter period time between...

10.1177/0961203307079300 article EN Lupus 2007-07-01

OBJETIVOS: Avaliar o consumo alimentar de crianças e adolescentes com artrite idiopática juvenil (AIJ) lúpus eritematoso sistêmico (LES) por recordatório 24 horas relacioná-lo características clínicas antropométricas os medicamentos empregados. MÉTODOS: Em estudo transversal, avaliamos recordatórios pacientes ambulatoriais. O estado nutricional foi classificado pelo CDC, 2000. Para cálculo da ingestão, utilizamos software NutWin UNIFESP-EPM. a análise quantitativa qualitativa, adotamos as...

10.1590/s0021-75572009000600007 article PT Jornal de Pediatria 2009-12-01
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