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A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry.
Papa, Riccardo; Doglio, Matteo; Lachmann, Helen J; Ozen, Seza; Frenkel, Joost; Simon, Anna; Neven, Bénédicte; Kuemmerle-Deschner, Jasmin; Ozgodan, Huri; Caorsi, Roberta; Federici, Silvia; Finetti, Martina; Trachana, Maria; Brunner, Jurgen; Bezrodnik, Liliana; Pinedo Gago, Mari Carmen; Maggio, Maria Cristina; Tsitsami, Elena; Al Suwairi, Wafaa; Espada, Graciela; Shcherbina, Anna; Aksu, Guzide; Ruperto, Nicolino; Martini, Alberto; Ceccherini, Isabella; Gattorno, Marco.
Afiliación
  • Papa R; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy. papariccardo86@gmail.com.
  • Doglio M; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Lachmann HJ; National Amyloidosis Centre, Royal Free Campus, University College Division of Medicine, London, UK.
  • Ozen S; Department of Pediatric Nephrology and Rheumatology, Hacettepe University, Ankara, Turkey.
  • Frenkel J; Division of Pediatrics, University Medical Center, Utrecht, The Netherlands.
  • Simon A; Department of Internal Medicine, Radboudumc Expertise Centre for Immunodeficiency and Autoinflammation, Radboudumc, Nijmegen, The Netherlands.
  • Neven B; Centre de reference national pour les Arthrites Juveniles, Unite d'Immunologie, Hematologie et Rhumatologie Pediatrique, Universite Paris-Descartes, IMAGINE Institute, Hopital Necker-Enfants Malades, Paris, France.
  • Kuemmerle-Deschner J; Rheumatologisches Zentrum/Ambulanzfur Autoimmunerkrankungen, Universitatsklinikum Tubingen, Tubingen, Germany.
  • Ozgodan H; Ic Hastaliklari ABD, Romatoloji BD, Istanbul Universitesi Cerrahpasa Tip Fakültesi, Istanbul, Turkey.
  • Caorsi R; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Federici S; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Finetti M; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Trachana M; Department of Pediatrics I, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Brunner J; Department fur Kinder-und Jugendheilkunde, Klinikfur Padiatrie I, Padiatrische Rheumatologie, Medizinische Universität Innsbruck, Innsbruck, Austria.
  • Bezrodnik L; Immunology Unit, Hospital de Ninos Ricardo Gutierrez, Buenos Aires, Argentina.
  • Pinedo Gago MC; Unidad de Reumatología Pediátrica, Hospital Universitario Cruces, Bilbao, Spain.
  • Maggio MC; Dipartimento Universitario, Ospedale dei Bambini, Palermo, Italy.
  • Tsitsami E; Pediatric Rheumatology Unit, 1st Department of Pediatrics, Children's Hospital Aghia Sophia, University of Athens, Athens, Greece.
  • Al Suwairi W; Department of Pediatrics, King Abdulaziz Medical City, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.
  • Espada G; Seccion Reumatologia, Hospital de Niños Ricardo Gutierrez, Buenos Aires, Argentina.
  • Shcherbina A; Research Institute for Paediatric Hematology, Moscow, Russia.
  • Aksu G; EgeUniversitesi Tip Fakultesi, Pediatrik Romatoloji, Izmir, Turkey.
  • Ruperto N; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Martini A; Direzione Scientifica, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Ceccherini I; UOC Medical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Gattorno M; EULAR Centre of Excellence in Rheumatology 2008-2018, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Orphanet J Rare Dis ; 12(1): 167, 2017 10 18.
Article en En | MEDLINE | ID: mdl-29047407
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema de Registros / Enfermedades Autoinflamatorias Hereditarias / Estudios de Asociación Genética Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema de Registros / Enfermedades Autoinflamatorias Hereditarias / Estudios de Asociación Genética Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Italia