Cargando…

Delayed diagnosis of Muckle-Wells syndrome – analysis of influencing factors

Detalles Bibliográficos
Autores principales:	Kuemmerle-Deschner, Jasmin B, Samba, Samuel D, Koné-Paut, Isabelle, Marie, Isabelle, Gramlich, Katharina, Hansmann, Sandra, Xenitidis, Theodoros, Benseler, Susanne M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403115/ http://dx.doi.org/10.1186/1546-0096-10-S1-A88

Ejemplares similares

IL-1 inhibition in Muckle-Wells-Syndrome: withdrawal resulting in rapid deterioration of hearing loss
por: Hansmann, S, et al.
Publicado: (2015)

Hypofertility in Muckle Wells syndrome and treatment with IL-1 targeting drugs
por: Meinzer, Ulrich, et al.
Publicado: (2011)

Early detection of sensorineural hearing loss in Muckle-Wells-syndrome
por: Kuemmerle-Deschner, Jasmin B., et al.
Publicado: (2015)

Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens
por: Kuemmerle-Deschner, Jasmin B, et al.
Publicado: (2013)

PReS-FINAL-2336: Induction of MDSCS in Muckle-Wells syndrome
por: Rieber, N, et al.
Publicado: (2013)

The phagocyte specific protein S100A12 as a novel biomarker in Muckle-Wells-Syndrome before and during therapy with Anakinra and Canakinumab (ACZ885)
por: Wittkowski, H, et al.
Publicado: (2008)

NLRP3 E311K mutation in a large family with Muckle-Wells syndrome - description of a heterogeneous phenotype and response to treatment
por: Kuemmerle-Deschner, Jasmin B, et al.
Publicado: (2011)

Determinants of health-related quality of life in children and adults with autoinflammatory diseases
por: Erbis, G, et al.
Publicado: (2015)

A large family having Muckle Wells Syndrome
por: Kilic, SS, et al.
Publicado: (2015)

Somatic NLRP3 mosaicism in Muckle-Wells syndrome
por: Gonzalez-Roca, E, et al.
Publicado: (2015)

Unmet psychosocial needs in CAPS
por: Erbis, G, et al.
Publicado: (2015)

Familial case of Muckle-Wells syndrome in the Russian population: a long way to the diagnosis
por: Salugina, Svetlana O, et al.
Publicado: (2014)

PW02-042 - Induction of MDSC in Muckle-Wells syndrome
por: Rieber, N, et al.
Publicado: (2013)

Dynamic knee joint function in children with juvenile idiopathic arthritis (JIA)
por: Hansmann, Sandra, et al.
Publicado: (2015)

A refractory heterogeneous Cryopyrin-Associated Periodic Syndrome (CAPS) phenotype related to V198M mutation responds to canakinumab - a case report
por: Hansmann, Sandra, et al.
Publicado: (2011)

Hearing improvement in a variant Muckle–Wells syndrome case in response to IL-1 receptor antagonism
por: Rynne, M, et al.
Publicado: (2005)

Cryopyrin-associated periodic syndromes (CAPS): report on two cases (Muckle-Wells syndrome (MWS) and CINCA/NOMID)
por: Salugina, SO, et al.
Publicado: (2011)

Anti-IL1ß-monoclonal antibody in a patient with Muckle-Wells Syndrome and renal transplantation - five years experience
por: Kortus-Götze, B, et al.
Publicado: (2015)

PReS-FINAL-2329: Validation of the autoinflammatory activity index (AIDAI)
por: Piram, M, et al.
Publicado: (2013)

Evidence based recommendations for diagnosis and treatment of cryopyrin-associated periodic syndromes (CAPS)
por: Haar, Nienke Ter, et al.
Publicado: (2014)

Evidence based recommendations for genetic diagnosis of Familial Mediterranean Fever
por: Giancane, Gabriella, et al.
Publicado: (2014)

Muckle–Wells syndrome: clinical perspectives
por: Tran, Tu-Anh
Publicado: (2017)

Resrip: a network dedicated to children and adolescents suffering from chronic rheumatic diseases in the Ile-de-France region
por: Rossi-Semerano, Linda, et al.
Publicado: (2014)

Abatacept in difficult-to-treat juvenile idiopathic arthritis
por: Kuemmerle-Deschner, Jasmin B, et al.
Publicado: (2008)

Living with autoinflammatory diseases: identifying unmet needs of children, adolescents and adults
por: Erbis, Gabriele, et al.
Publicado: (2018)

Management of Monogenic IL-1 Mediated Autoinflammatory Diseases in Childhood
por: Welzel, Tatjana, et al.
Publicado: (2021)

Colchicine – an effective treatment for children with a clinical diagnosis of autoinflammatory diseases without pathogenic gene variants
por: Welzel, Tatjana, et al.
Publicado: (2021)

The use of colchicine in PFAPA syndrome, the french experience and literature review
por: Dusser, Perrine, et al.
Publicado: (2014)

Canakinumab treat-to target strategies increase complete response rate in CAPS
por: Kuemmerle-Deschner, J, et al.
Publicado: (2015)

Recommendations for the management of autoinflammatory diseases
por: ter Haar, N, et al.
Publicado: (2015)

Colchicine Effectiveness and Safety in Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis
por: Welzel, Tatjana, et al.
Publicado: (2021)

P02-028 - Muckle-Wells syndrome and renal transplantation
por: Kortus-Götze, B, et al.
Publicado: (2013)

Evidence based recommendations for diagnosis and treatment of tumor necrosis factor receptor-1 associated periodic syndrome (TRAPS)
por: Haar, Nienke Ter, et al.
Publicado: (2014)

Evidence based recommendations for diagnosis and management of mevalonate kinase defiency (MKD)
por: Haar, Nienke Ter, et al.
Publicado: (2014)

PReS-FINAL-2208: Sacroilitis with propionibacterium acnes in a child
por: Galeotti, C, et al.
Publicado: (2013)

NLRP3 Q703K and TNFRSF1A R92Q mutations in a patient with auto inflammatory disease
por: von Mühlenen, I, et al.
Publicado: (2015)

Autologous stem cell transplantation in two children with disabling pansclerotic morphea
por: Moll, M, et al.
Publicado: (2011)

Muckle–Wells syndrome in an Indian family associated with NLRP3 mutation
por: Abdulla, MC, et al.
Publicado: (2015)

Efficacy of oral versus subcutaneous methotrexate in children with juvenile idiopathic arthritis
por: Tzaribachev, N, et al.
Publicado: (2008)

Familial Mediterranean Fever (FMF) before the age of one year
por: Delion, F, et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_0iivh2kgiuofqocbk96jjgm29i