A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients.
about
A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean FeverAutoinflammatory gene mutations in Behçet's diseaseWorking the endless puzzle of hereditary autoinflammatory disorders.Familial mediterranean Fever: a retrospective clinical and molecular study in the East of anatolia region of Turkey.The spectrum of autoinflammatory diseases: recent bench to bedside observationsFamilial Mediterranean fever: genotype-phenotype correlations in Japanese patients.Guidelines for the genetic diagnosis of hereditary recurrent fevers.Clinical and Genetic Features of Korean Patients with Recurrent Fever and Multi-System Inflammation without Infectious or Autoimmune EvidenceS100A12 is a novel molecular marker differentiating systemic-onset juvenile idiopathic arthritis from other causes of fever of unknown origin.The clinical spectrum of 94 patients carrying a single mutated MEFV allele.Inheritance of autoinflammatory diseases: shifting paradigms and nomenclature.Monogenic autoinflammatory diseases.The labyrinth of autoinflammatory disorders: a snapshot on the activity of a third-level center in Italy.Lights and shadows in autoinflammatory syndromes from the childhood and adulthood perspective.Clinical genetic testing of periodic fever syndromesCaution Should be Used in the Recognition of Adult-Onset Autoinflammatory Disorders: Facts or Fiction?Next-generation sequencing and its initial applications for molecular diagnosis of systemic auto-inflammatory diseases.PFAPA syndrome and Behçet's disease: a comparison of two medical entities based on the clinical interviews performed by three different specialists.Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers.[Genetic fever syndromes. Hereditary recurrent (periodic) fever syndromes].Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population.Hereditary autoinflammatory syndromes: a Brazilian multicenter study.Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children.Validation of a diagnostic score for the diagnosis of autoinflammatory diseases in adults.Development and preliminary validation of a diagnostic score for identifying patients affected with adult-onset autoinflammatory disorders.Intermittent fevers, abdominal pain, and elevated inflammatory markers.Role of genetics in pediatric rheumatology.Autoinflammatory disorders and patients with isolated serosal involvement
P2860
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P2860
A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
A decision tree for genetic di ...... fever in unselected patients.
@ast
A decision tree for genetic di ...... fever in unselected patients.
@en
type
label
A decision tree for genetic di ...... fever in unselected patients.
@ast
A decision tree for genetic di ...... fever in unselected patients.
@en
prefLabel
A decision tree for genetic di ...... fever in unselected patients.
@ast
A decision tree for genetic di ...... fever in unselected patients.
@en
P2093
P2860
P356
P1476
A decision tree for genetic di ...... fever in unselected patients.
@en
P2093
A Le Quellec
C Jorgensen
C Rittore-Domingo
I Koné-Paut
L Federici
P2860
P304
P356
10.1136/ARD.2006.054304
P407
P577
2006-05-17T00:00:00Z