Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Hereditary periodic fever syndromes"'
Autor:
Marianna Pinheiro Moraes de Moraes, Renan Rodrigues Neves Ribeiro do Nascimento, Fabiano Ferreira Abrantes, José Luiz Pedroso, Sandro Félix Perazzio, Orlando Graziani Povoas Barsottini
Publikováno v:
Brain Sciences, Vol 13, Iss 9, p 1351 (2023)
Autoinflammatory disorders encompass a wide range of conditions with systemic and neurological symptoms, which can be acquired or inherited. These diseases are characterized by an abnormal response of the innate immune system, leading to an excessive
Externí odkaz:
https://doaj.org/article/8d4f520a2c634fbab6fd92a7be99e634
Publikováno v:
Seminars in arthritis and rheumatism. 51(6)
Background The development of biological treatments has transformed the management of a broad spectrum of autoimmune/inflammatory diseases. However, little is known about their use in solid-organ transplant recipients. This study aimed to evaluate co
Publikováno v:
Oxford Textbook of Medicine
The hereditary periodic fever syndromes or hereditary autoinflammatory diseases are disorders of innate immunity that mostly present in childhood and are characterized by recurrent, self-limiting, seemingly unprovoked episodes of fever and systemic i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4176ff1ccb0a0708fe08ae9f7ad9fe
https://doi.org/10.1093/med/9780198746690.003.0240
https://doi.org/10.1093/med/9780198746690.003.0240
Akademický článek
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Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 12, Pp 6469-6484 (2017)
Familial Mediterranean fever, an autosomal recessive disorder, is a member of the periodic fever syndromes, and considered to be the most common cause of recurrent febrile episodes in children. It is important to understand the disorder as familial M
Autor:
Antonio Torrelo, G. Xirotagaros, Angela Hernández-Martín, L. Prieto-Torres, Lucero Noguera-Morel, S. Hernández-Ostiz
Publikováno v:
Actas Dermo-Sifiliográficas (English Edition). 108:609-619
Monogenic autoinflammatory diseases are a heterogeneous emergent group of conditions that are currently under intensive study. We review the etiopathogenesis of these syndromes and their principal manifestations. Our aim is to propose a classificatio
Autor:
Hafize Emine Sönmez, Seza Ozen
Publikováno v:
International Immunology. 29:393-400
Inflammasomes are important elements of the innate immune defense. The most common autoinflammatory syndromes, as well a number of rare ones, are due to hereditary defects in the inflammasomes, hence are called inflammasomopathies. The recent clinica
Autor:
Stefano Gentileschi, Donato Rigante, Claudia Fabiani, Orso Maria Lucherini, Ida Orlando, Luca Cantarini, Antonio Vitale, Antonella Simpatico, Anna De Palma, Bruno Frediani, Mauro Galeazzi, Jurgen Sota
Publikováno v:
Internal and Emergency Medicine. 12:605-611
The study aims are to describe the activity of our Unit on the diagnostics of monogenic autoinflammatory diseases (AIDs), and to apply the clinical classification criteria for periodic fevers from the Eurofever Registry to our cohort of patients, thu
Publikováno v:
Europe PubMed Central
Monogenic autoinflammatory disorders (AIDs) are rare diseases driven by cytokine-mediated extraordinary sterile inflammation that results from the activation of innate immune pathways. The clinical hallmark of these diseases is the recurrence of ster
Akademický článek
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