Ivan Foeldvari

ORCID: 0000-0003-0659-5298
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About
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Research Areas
  • Autoimmune and Inflammatory Disorders Research
  • Systemic Sclerosis and Related Diseases
  • Adolescent and Pediatric Healthcare
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Acute Lymphoblastic Leukemia research
  • Inflammasome and immune disorders
  • Ocular Diseases and Behçet’s Syndrome
  • Systemic Lupus Erythematosus Research
  • Dermatologic Treatments and Research
  • Dermatological and Skeletal Disorders
  • Rheumatoid Arthritis Research and Therapies
  • Childhood Cancer Survivors' Quality of Life
  • Inflammatory Myopathies and Dermatomyositis
  • Immunodeficiency and Autoimmune Disorders
  • Pharmaceutical studies and practices
  • Mast cells and histamine
  • Pulmonary Hypertension Research and Treatments
  • Eosinophilic Disorders and Syndromes
  • Kawasaki Disease and Coronary Complications
  • Autoimmune Bullous Skin Diseases
  • Skin Diseases and Diabetes
  • Otitis Media and Relapsing Polychondritis
  • Renal Diseases and Glomerulopathies
  • Lymphoma Diagnosis and Treatment
  • Child and Adolescent Health

Schön Klinik Hamburg Eilbek
2016-2025

Durham VA Medical Center
2022-2024

Kinderkrebs-Zentrum Hamburg
2015-2024

German Center for Pediatric and Adolescent Rheumatology
2018-2024

Asklepios
2015-2024

University of North Carolina at Chapel Hill
2022-2024

AID Atlanta
2024

American College of Rheumatology
2022-2024

Emory University
2022-2024

Convergence
2024

Tumor necrosis factor (TNF) has a pathogenic role in juvenile rheumatoid arthritis. We evaluated the efficacy and safety of adalimumab, fully human monoclonal anti-TNF antibody, children with polyarticular-course arthritis.Patients 4 to 17 years age active arthritis who had previously received treatment nonsteroidal antiinflammatory drugs underwent stratification according methotrexate use 24 mg adalimumab per square meter body-surface area (maximum dose, 40 mg) subcutaneously every other...

10.1056/nejmoa0706290 article EN New England Journal of Medicine 2008-08-20

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

The modified Rodnan skin score (mRSS) is a measure of thickness and used as primary or secondary outcome in clinical trials systemic sclerosis (scleroderma). This state-of-art review provides historical perspective the development mRSS, summarizes performance mRSS an measure, guidance on assessing makes recommendations for incorporation into trials.

10.5301/jsrd.5000231 article EN Journal of Scleroderma and Related Disorders 2017-01-01

Objective: Etanercept monotherapy has been studied and approved for treatment of polyarticular juvenile idiopathic arthritis (JIA). The following study evaluates the safety efficacy combination therapy etanercept methotrexate compared to in JIA. Methods: We perfomed an open, non-randomised on patients who had previously failed respond at least one disease-modifying antirheumatic drug (DMARD). A total 722 with JIA whom 1 item follow-up data was recorded were identified; these, 118 treated...

10.1136/ard.2007.087593 article EN Annals of the Rheumatic Diseases 2008-04-15

<h3>Context</h3>Novel therapies have improved the remission rate in chronic inflammatory disorders including juvenile idiopathic arthritis (JIA). Therefore, strategies of tapering therapy and reliable parameters for detecting subclinical inflammation now become challenging questions.<h3>Objectives</h3>To analyze whether longer methotrexate treatment during JIA prevents flares after withdrawal medication specific biomarkers identify patients at risk flares.<h3>Design, Setting,...

10.1001/jama.2010.375 article EN JAMA 2010-04-07

Abstract The term ‘sclerosing diseases of the skin' comprises specific dermatological entities, which have fibrotic changes skin in common. These mostly manifest different clinical subtypes according to cutaneous and extracutaneous involvement can sometimes be difficult distinguish from each other. present guideline focuses on characteristic histopathological features, diagnostic scores serum autoantibodies most useful for differential diagnosis. In addition, current strategies first‐...

10.1111/jdv.14458 article EN Journal of the European Academy of Dermatology and Venereology 2017-08-09

In 2012, a European initiative called Single Hub and Access point for pediatric Rheumatology in Europe (SHARE) was launched to optimise disseminate diagnostic management regimens children young adults with rheumatic diseases. Juvenile idiopathic arthritis (JIA) is the most common disease uveitis possibly its devastating extra-articular manifestation. Evidence-based guidelines are sparse mostly based on physicians' experience. Consequently, treatment practices differ widely, within between...

10.1136/annrheumdis-2018-213131 article EN cc-by Annals of the Rheumatic Diseases 2018-03-28
Alessandro Consolaro Gabriella Giancane Alessandra Alongi E. H. Pieter van Dijkhuizen Amita Aggarwal and 95 more Sulaiman M. Al‐Mayouf Francesca Bovis Jaime de Inocencio Arocena Erkan Demirkaya Berit Flatø Dirk Foell Stella Maris Garay Călin Lazăr Daniel J. Lovell Carolina Montobbio Päivi Miettunen Dimitrina Mihaylova Susan Nielsen Ilonka Orbán Ingrîda Rumba-Rozenfelde Cláudia Saad Magalhães Nahid Shafaie Gordana Sušić Maria Trachana Nico Wulffraat Angela Pistorio Alberto Martini Nicolino Ruperto Angelo Ravelli Reem Abdwani Yahya Aghighi M. Aïche Constantin Ailioaie Nuray Aktay Ayaz Safiya Al‐Abrawi Е.I. Alexeeva Jordi Antón Adriana Apostol O Arguedas Tadej Avčin Patrizia Barone Lillemor Berntson Alina Boteanu Yaryna Boyko Rubén Burgos‐Vargas Inmaculada Calvo Penadés Gaëlle Chédeville Rolando Cimaz Adele Civino Rita Consolini Tamás Constantin Rubén Cuttica Inmaculada Tomás Neil A. Martin Silvia Magni‐Manzoni Carmen De Cunto Pavla Doležalová Maria Ekelund Yasser El Miedany Graciela Espada Anne Estmann Christensen Ivan Foeldvari Romina Gallizzi Gerd Ganser V. Gerloni Johannes‐Peter Haas Liora Harel Miroslav Harjaček Soad Hashad Troels Herlin Cristina Herrera Michaël Hofer Dirk Holzinger Gerd Horneff Hans-Iko Huppertz N Iagăru Amparo Ibanez Estrella Maka Ioseliani Rik Joos Sheila Knupp Feitosa de Oliveira Sylvia Kamphuis Özgür Kasapçopur María Martha Katsicas Raju Khubchandani Anuela Kondi Liisa Kröger Francesco La Torre Matilda Láday Pekka Lahdenne Maria Cristina Maggio Maria Greca Magnolia Clara Malagón Merja Malin Silvana Martino José Melo‐Gomes Pablo Mesa-del-Castillo Andrea Militaru Kirsten Minden Angela Miniaci Mohammad Hasan Moradinejad

10.1016/s2352-4642(19)30027-6 article EN The Lancet Child & Adolescent Health 2019-02-26

Abstract Objective We previously documented that abatacept was effective and safe in patients with juvenile idiopathic arthritis (JIA) who had not achieved a satisfactory clinical response disease‐modifying antirheumatic drugs or tumor necrosis factor blockade. Here, we report results from the long‐term extension (LTE) phase of study. Methods This describes long‐term, open‐label double‐blind, randomized, controlled withdrawal trial 190 JIA ages 6–17 years. Children were treated 10 mg/kg...

10.1002/art.27431 article EN Arthritis & Rheumatism 2010-02-26

To determine the clinical and immunologic features of systemic sclerosis (SSc) in a large group children describe evolution disease compare it with adult form.Data on 153 patients juvenile SSc collected from 55 pediatric rheumatology centers Europe, Asia, South North America were analyzed. Demographic, clinical, characteristics at onset, diagnosis, during course evaluated.Raynaud's phenomenon was most frequent symptom, followed by skin induration approximately 75% patients. Musculoskeletal...

10.1002/art.22207 article EN Arthritis & Rheumatism 2006-11-28

Abstract Objective To develop criteria for the classification of systemic sclerosis (SSc) in children (juvenile SSc). Methods The study consisted 3 phases: 1) collection data on signs and symptoms actual patients with juvenile SSc that are useful defining involvement a particular organ; 2) selection parameters essential preparation set provisional (PCC) using 2 Delphi surveys; 3) consensus conference consisting steps: discussion rating clinical profiles 160 definite SSc, possible or other...

10.1002/art.22551 article EN Arthritis Care & Research 2007-02-28

Abstract Introduction In the present study, we analysed in detail nuclear autoantibodies and their associations systemic sclerosis (SSc) patients included German Network for Systemic Scleroderma Registry. Methods Sera of 863 were according to a standardised protocol including immunofluorescence, immunoprecipitation, line immunoassay immunodiffusion. Results Antinuclear antibodies (ANA) detected 94.2% patients. 81.6%, at least one highly associated with SSc or overlap syndromes scleroderma...

10.1186/ar3495 article EN cc-by Arthritis Research & Therapy 2011-10-21

To validate a core set of outcome measures for the evaluation response to treatment in patients with juvenile dermatomyositis (DM).In 2001, preliminary consensus-derived evaluating therapy DM was established. In present study, validated through an evidence-based, large-scale data collection that led enrollment 294 from 36 countries. Consecutive active disease were assessed at baseline and after 6 months. The validation procedures included assessment feasibility, responsiveness, discriminant...

10.1002/art.23248 article EN Arthritis Care & Research 2007-12-28

<h3>Objective</h3> To assess the long-term efficacy and safety of infliximab plus methotrexate in juvenile rheumatoid arthritis (JRA). <h3>Methods</h3> Patients eligible for open-label extension (OLE, weeks 52–204) received 3–6 mg/kg every 8 methotrexate. <h3>Results</h3> Of 78/122 (64%) children entering OLE, 42 discontinued infliximab, most commonly due to consent withdrawal (11 patients), lack (eight patients) or patient/physician/sponsor requirement patients). Infliximab (mean dose 4.4...

10.1136/ard.2009.100354 article EN Annals of the Rheumatic Diseases 2010-03-17

<h3>Abstract</h3> Antifungal resistance in pathogenic fungi is a growing global health concern. Non-pathogenic laboratory strains of <i>Saccharomyces cerevisiae</i> are useful model for studying mechanisms antifungal that relevant to understanding the same processes fungi. We developed series lab modules which high school students used experimental evolution study by isolating azole-resistant <i>S. and examining genetic basis resistance. All 99 sequenced clones from these experiments...

10.1136/annrheumdis-2012-203046 article EN cc-by-nc Annals of the Rheumatic Diseases 2013-05-21

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children and adolescents. Immunomodulatory drugs are used frequently its treatment. Using nominal group technique (NGT) Delphi method, we created a multidisciplinary, evidence- consensus-based treatment guideline for JIA based on systematic literature analysis three consensus conferences. Conferences were headed by professional moderator attended representatives who had been nominated their scientific societies or...

10.1016/j.clim.2011.10.003 article EN cc-by-nc-nd Clinical Immunology 2011-10-29
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