MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes.
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Complete remission in 3 of 3 anti-IL-6-treated patients with Schnitzler syndrome.
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Successful canakinumab treatment identifies IL-1β as a pivotal mediator in Schnitzler syndrome.
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Anakinra: An effective treatment in the Schnitzler syndrome.
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Canakinumab: In Patients with Cryopyrin-Associated Periodic Syndromes.
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Sustained remission of symptoms and improved health-related quality of life in patients with cryopyrin-associated periodic syndrome treated with canakinumab: results of a double-blind placebo-controlled randomized withdrawal study.
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NLRP3 E311K mutation in a large family with Muckle-Wells syndrome - description of a heterogeneous phenotype and response to treatment.
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Genetic analysis of C5a receptors in neutrophils from patients with familial Mediterranean fever.
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Decreased vitamin D levels in patients with familial mediterranean fever.
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Cochlear involvement in Familial Mediterranean Fever: A new feature of an old disease.
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PFAPA syndrome in siblings. Is there a genetic background?
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Cephalometric evaluation of children with familial Mediterranean fever.
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Evaluation of the mean platelet volume in children with familial Mediterranean fever.
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Abnormal heart rate variability in AA amyloidosis of familial Mediterranean fever.
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The value of procalcitonin measurements in children with familial Mediterranean fever.
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Homozygous M694V as a risk factor for amyloidosis in Turkish FMF patients.
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Leucopenia Resoluted With Colchicine in Familial Mediterranean Fever.
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Myalgia as a symptom of familial Mediterranean fever in children.
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'Silent carriage' of two familial Mediterranean fever gene mutations in large families with only a single identified patient.
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Effects of anti-tumor necrosis factor agents for familial mediterranean fever patients with chronic arthritis and/or sacroiliitis who were resistant to colchicine treatment.
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Coexistence of vasculitides with Familial Mediterranean Fever.
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P-wave dispersion in systemic AA amyloidosis of familial Mediterranean fever.
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Vascular comorbidities in familial Mediterranean fever.
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[PFAPA syndrome: Study of 10 cases.]
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Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children.
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