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Akademický článek

Application of systems biology-based in silico tools to optimize treatment strategy identification in Still’s disease

Autor: Cristina Segú-Vergés, Mireia Coma, Christoph Kessel, Serge Smeets, Dirk Foell, Anna Aldea

Publikováno v: Arthritis Research & Therapy, Vol 23, Iss 1, Pp 1-12 (2021)

Abstract Background Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are manifestations of an autoinflammatory disorder with complex pathophysiology and significant morbidity, together also termed Still’s disea

Externí odkaz: https://doaj.org/article/90648241b76a4414a9ae761e3e05b9b4

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Time intervals in the care pathway to cancer diagnosis during the COVID-19 pandemic: A large retrospective study from a high-volume center

Autor: Xavier Bosch, Elisabet Montori‐Palacin, Rosa Martínez‐Ferrer, Anna Aldea, Pedro Moreno, Alfonso López‐Soto

Publikováno v: International journal of cancer. 152(3)

Despite extensive research on cancer care during the COVID-19 pandemic, evidence on the impact on prediagnostic time intervals is lacking. To better understand how COVID-19 changed the pathway to diagnosis of cancer, we examined the length of interva

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843580488f53c7e6ce7852ef097311bc
https://pubmed.ncbi.nlm.nih.gov/36053784

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Everolimus plus minimized tacrolimus on kidney function in liver transplantation: REDUCE, a prospective, randomized controlled study

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona
Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

BACKGROUND AND AIM: reduction in calcineurin inhibitor levels is considered crucial to decrease the incidence of kidney dysfunction in liver transplant (LT) recipients. The aim of this study was to evaluate the safety and impact of everolimus plus re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7879ad58eede2c8120168984d2b4c405
http://hdl.handle.net/2445/187444

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Application of systems biology-based in silico tools to optimize treatment strategy identification in Still’s disease

Autor: Anna Aldea, Mireia Coma, Serge J. Smeets, Christoph Kessel, Dirk Foell, Cristina Segú-Vergés

Publikováno v: Arthritis Research & Therapy
Arthritis Research & Therapy, Vol 23, Iss 1, Pp 1-12 (2021)

Background Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are manifestations of an autoinflammatory disorder with complex pathophysiology and significant morbidity, together also termed Still’s disease. The o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7832a14a27ccd1be72fd44a953036cb9
http://europepmc.org/articles/PMC8063416

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Etanercept plus colchicine treatment in a child with tumour necrosis factor receptor-associated periodic syndrome abolishes auto-inflammatory episodes without normalising the subclinical acute phase response

Autor: S Plaza, Samuel Gómez, Anna Aldea, Jordi Yagüe, Pilar Bahillo, Jordi Vives, Pilar Solís, Josefa Rius, Juan I. Aróstegui, Teresa Cantero

Publikováno v: European Journal of Pediatrics. 164:13-16

We investigated the cause of hereditary periodic fever syndrome in a Spanish child with recurrent long episodes of fever, migratory skin rash, myalgia, arthralgia, conjunctivitis and abdominal pain. Infectious and autoimmune causes were ruled out. No

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52d5ae6fe9508d049fca5d20e134cfe0
https://doi.org/10.1007/s00431-004-1563-1

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Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with theCIAS1/PYPAF1/NALP3gene

Autor: Maria Jesús Rua, Eduardo Ramos, Jordi Yagüe, María Antonia González-Enseñat, Jordi Vives, Juan I. Aróstegui, Consuelo Modesto, Federico Arguelles, S Plaza, Anna Aldea, Josefa Rius

Publikováno v: Arthritis & Rheumatism. 50:4045-4050

Objective To investigate the involvement of the CIAS1/PYPAF1/NALP3 gene in 7 unrelated Spanish families with recurrent autoinflammatory diseases characterized by early onset, recurrent fever, and a chronic urticarial rash, in whom a clinical diagnosi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::78fcaa6a885c505143994bb47d4bbab9
https://doi.org/10.1002/art.20633

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A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: An unusual familial Mediterranean fever phenotype or another MEFV-associated periodic

Autor: Josep M. Campistol, Jordi Yagüe, Juan I. Aróstegui, Josefa Rius, Anna Aldea, Montserrat Masó, Jordi Vives

Publikováno v: American Journal of Medical Genetics Part A. :67-73

Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurring short attacks of fever and serositis. Secondary AA amyloidosis is the worst complication of the disease and often determines the prognosis. The MEFV gene,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54fcb503f7cbf8cf7efdd17ec5986421
https://doi.org/10.1002/ajmg.a.20296

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The west side story: MEFV haplotype in Spanish FMF patients and controls, and evidence of high LD and a recombination 'hot-spot' at the MEFV locus

Autor: Anna, Aldea, Francesc, Calafell, Juan I, Aróstegui, Oscar, Lao, Josefa, Rius, Susana, Plaza, Montserrat, Masó, Jordi, Vives, Joan, Buades, Jordi, Yagüe

Publikováno v: Human mutation. 23(4)

Mutations at the MEFV gene cause, with various degrees of penetrance, familial Mediterranean fever (FMF). This disease is more prevalent in the Middle East than elsewhere, and most studies have focused on those populations. However, FMF occurs also i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d10d90cb138e8a807f60426cfdbe799f
https://pubmed.ncbi.nlm.nih.gov/15024744

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