Cargando…

Chronic granulomatous disease in an infant with sweet syndrome

Detalles Bibliográficos
Autores principales:	Hanedan, S, Sahin, B, Ayaz, N Aktay, Aldemir, H
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2008
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3333934/ http://dx.doi.org/10.1186/1546-0096-6-S1-P137

Ejemplares similares

PReS-FINAL-2057: Systemic onset JIA with coronary artery dilatation
por: Aktay Ayaz, N, et al.
Publicado: (2013)

PReS-FINAL-2221: An earliest diagnosis of FMF
por: Keskindemirci, G, et al.
Publicado: (2013)

PReS-FINAL-2222: FMF presenting with the features of malignancy
por: Keskindemirci, G, et al.
Publicado: (2013)

PReS-FINAL-2220: Cochlear involvement in FMF
por: Keskindemirci, G, et al.
Publicado: (2013)

A case of chronic recurrent multifocal osteomyelýtýs successfully treated with etanercept
por: Aktay Ayaz, N, et al.
Publicado: (2008)

Chronic granulomatous disease (CGD) presenting as quotidian fever
por: Moenkemoeller, K, et al.
Publicado: (2008)

A novel therapeutic approach for macrophage actıvatıon syndrome due to SoJIA
por: Ayaz, Nuray Aktay, et al.
Publicado: (2011)

Turkish Pediatric Rheumatology Society consensus statements on systemic onset juvenile idiopathic arthritis in Turkey
por: Sozeri, B, et al.
Publicado: (2015)

Chronic granulomatous disease associated with systemic lupus erythematosus and systemic onset juvenile idiopathic arthritis
por: Parvaneh, Vadood Javadi, et al.
Publicado: (2014)

Features of enthesitis related arthritis in Turkish children
por: Akkus, K, et al.
Publicado: (2008)

Musculoskeletal sonography in juvenile systemic lupus erythematosus
por: Demirkaya, E, et al.
Publicado: (2008)

MEFV mutations in systemic JIA
por: Aktay Ayaz, N, et al.
Publicado: (2008)

Differences in the severity of the phenotype of children and adolescents with Familial Mediterranean Fever residing in Turkey and Germany
por: Ayaz, N Aktay, et al.
Publicado: (2008)

Effect of infliximab in sweet’s syndrome-pyoderma gangraenosum overlap syndrome
por: Mahler, Birgitte, et al.
Publicado: (2014)

A safe protocol for tuberculin test assessment in a country where BCG vaccination is mandatory
por: Ayaz, N Aktay, et al.
Publicado: (2008)

PReS-FINAL-2219: Evaluation of autonomic function in FMF
por: Aktay Ayaz, N, et al.
Publicado: (2013)

Neutrophlic dermatosis (Sweet's syndrome-like) induced by paracetamol
por: Culla, M Teresa Dordal, et al.
Publicado: (2014)

Anakinra for secondary amyloidosis in an adolescent with FMF and Behcet Disease
por: Bilginer, Y, et al.
Publicado: (2008)

Does unity of Familial Mediterranean fever with juvenile idiopathic arthritis affect the outcome?
por: Topaloglu, R, et al.
Publicado: (2008)

Assessment of children presenting with rheumatic complaints to a tertiary center in Turkey: differences in an Eastern Mediterranean population
por: Bircan Cavkaytar, Ö, et al.
Publicado: (2008)

Behcet Disease: treatment of vascular involvement in children
por: Bilginer, Y, et al.
Publicado: (2008)

A 5-year case review of granulomatous mastitis
por: O'Connor, A, et al.
Publicado: (2009)

Interstial granulomatous dermatitis as initial presentation of juvenile mixed connective disease and its response to tacrolimus
por: Jung, Lawrence, et al.
Publicado: (2012)

Sweet's syndrome in a patient with compound heterozygous mutations in the Mediterranean fever gene (MEFV)
por: Michelson, M, et al.
Publicado: (2015)

An infant with Cushing syndrome
por: Sng, Andrew, et al.
Publicado: (2015)

P01-048 – Systemic onset JIA with coronary artery dilation
por: Ayaz, N Aktay, et al.
Publicado: (2013)

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF alpha monoclonal antibodies
por: Moshous, D, et al.
Publicado: (2011)

P01-018 – An earliest diagnosis of FMF
por: Ayaz, N Aktay, et al.
Publicado: (2013)

P01-017 – FMF presention with features of malignancy
por: Ayaz, N Aktay, et al.
Publicado: (2013)

Genetic transformation of sweet oranges to over-express SABP2 gene
por: Attílio, Lísia Borges, et al.
Publicado: (2014)

Congenital central hypoventilation syndrome with hyperinsulinemia in an infant
por: Ganti, Uma, et al.
Publicado: (2015)

27 Single center inception cohort of enthesitis-related arthritis: spectrum of characteristics, course and treatment approaches
por: Demirkan, Fatma Gül, et al.
Publicado: (2022)

P59 - Kartagener syndrome in infant – case report
por: Hristova, Tanya, et al.
Publicado: (2014)

“Tasting” fructose with pancreatic beta-cells: modulation of insulin release by sweet taste receptor signaling and its role in metabolic diseases
por: Kyriazis, George A, et al.
Publicado: (2012)

PReS-FINAL-2204: Developing of a new scale for assessing the adherence to colchicines treatment in pediatric patients with FMF
por: Yesilkaya, S, et al.
Publicado: (2013)

Chronic granulomatous disease
por: Naveen, Kikkeri Narayanasetty, et al.
Publicado: (2015)

Familial Mediterranean Fever: Diagnosing as Early as 3 Months of Age
por: Keskindemirci, Gonca, et al.
Publicado: (2014)

Macrophage activation syndrome in a newborn infant born to a untreated mother with adult onset still disease
por: Rhim, Jung Woo, et al.
Publicado: (2014)

Dissecting the heterogeneity of macrophage activation syndrome
por: Davì, Sergio, et al.
Publicado: (2014)

A138 SERRATED POLYPOSIS SYNDROME IN INFLAMMATORY BOWEL DISEASE: A SEQUELAE OF CHRONIC DISEASE ACTIVITY OR NEW WHO PHENOTYPE?
por: Jiang, S X, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_5s8e3oq11fn5qhp2kmqtikefks