Familial Mediterranean fever is no longer a rare disease in Japan

scientific article published on 30 July 2016

Familial Mediterranean fever is no longer a rare disease in Japan is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1186/S13075-016-1071-5
P932PMC publication ID4967332
P698PubMed publication ID27473114

P50authorMasataka UmedaQ56987269
Atsushi KawakamiQ61999596
Tomohiro KogaQ88065202
Yoshifumi UbaraQ91307295
P2093author name stringKoh-Ichiro Yoshiura
Tadashi Nakamura
Katsumi Eguchi
Kiyoshi Migita
Michio Yasunami
Chieko Kawahara
Nozomi Iwanaga
Yasumori Izumi
Satoshi Yamasaki
Yuka Jiuchi
Akihiro Yachie
Fumiaki Nonaka
Junya Masumoto
Kazunaga Agematsu
Toshimasa Shimizu
Yoshikazu Nakashima
Keita Fujikawa
P2860cites workThe spectrum of Familial Mediterranean Fever (FMF) mutationsQ34314032
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsQ34390765
Clinical disease among patients heterozygous for familial Mediterranean feverQ34983754
Gain-of-function Pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in miceQ35086225
Severe disease in patients with rheumatoid arthritis carrying a mutation in the Mediterranean fever geneQ35555791
Familial Mediterranean fever: genotype-phenotype correlations in Japanese patientsQ36247836
Familial mediterranean fever in Arabs.Q36431512
Clinical features and functional significance of the P369S/R408Q variant in pyrin, the familial Mediterranean fever proteinQ36603948
Familial Mediterranean fever with a single MEFV mutation: where is the second hit?Q37366257
Clinical and genetic features of familial Mediterranean fever in JapanQ37521441
The spectrum of MEFV clinical presentations--is it familial Mediterranean fever only?Q37616913
Diagnostic criteria of familial Mediterranean feverQ38178456
Evidence-based recommendations for genetic diagnosis of familial Mediterranean feverQ38335115
The myths we believed in familial Mediterranean fever: what have we learned in the past years?Q38400573
Adult Onset Still's Disease: A Review on Diagnostic Workup and Treatment OptionsQ38797433
The carrier rate and spectrum of MEFV gene mutations in central and southeastern European populations.Q40138045
Familial Mediterranean fever in heterozygotes: are we able to accurately diagnose the disease in very young children?Q40254151
Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in childrenQ40255424
Familial Mediterranean fever in JapanQ40269732
Familial Mediterranean FeVer gene (MEFV) mutations as a modifier of systemic lupus erythematosusQ40289119
The structural effect of the E148Q MEFV mutation on the pyrin protein: a study using a quantum chemistry model.Q40324351
MEFV mutations in systemic onset juvenile idiopathic arthritisQ40405557
MEFV mutation analysis of familial Mediterranean fever in Japan.Q40425023
MEFV analysis is of particularly weak diagnostic value for recurrent fevers in Western European Caucasian patientsQ40495186
Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation?Q40550727
The E148Q MEFV allele is not implicated in the development of familial Mediterranean fever.Q40550949
Familial Mediterranean fever: high gene frequency and heterogeneous disease among an Israeli-Arab population.Q40620194
Criteria for the diagnosis of familial Mediterranean feverQ40645936
Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health.Q47611050
Familial Mediterranean feverQ74309346
Acute phase response and evolution of familial Mediterranean feverQ77397098
P921main subjectJapanQ17
rare diseaseQ929833
familial Mediterranean feverQ1144618
P304page(s)175
P577publication date2016-07-30
P1433published inArthritis Research and TherapyQ15757229
P1476titleFamilial Mediterranean fever is no longer a rare disease in Japan
P478volume18

Reverse relations

cites work (P2860)
Q64041896A Rare Case of Cryopyrin-associated Periodic Syndrome in an Elderly Woman with NLRP3 and MEFV Mutations
Q40040838AA Amyloidosis and Atypical Familial Mediterranean Fever with Exon 2 and 3 Mutations
Q64101692An adult case of atypical familial Mediterranean fever (pyrin-associated autoinflammatory disease) similar to adult-onset Still's disease
Q58590120Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics
Q91776376Atypical Familial Mediterranean Fever Presenting with Recurrent Migratory Polyarthritis
Q40044427Cold Exposure Related Fever with an Mediterranean Fever (MEFV) Gene Mutation
Q93389870Exon 2: Is it the good police in familial mediterranean fever?
Q90068673Familial Mediterranean Fever Is Important in the Differential Diagnosis of Recurrent Aseptic Meningitis in Japan
Q88742023Familial Mediterranean Fever Mutations in a Patient with Periodic Episodes of Systemic Pain Deriving from Cancer Bone Metastases
Q91711832Familial Mediterranean Fever in Chinese Children: A Case Series
Q53703053Five Cases of Familial Mediterranean Fever in Japan: The Relationship with MEFV Mutations.
Q38746358Geoepidemiology and Immunologic Features of Autoinflammatory Diseases: a Comprehensive Review.
Q59336394Musculoskeletal manifestations occur predominantly in patients with later-onset familial Mediterranean fever: Data from a multicenter, prospective national cohort study in Japan
Q90589005Necessity of Utilizing Physiological Glucocorticoids for Managing Familial Mediterranean Fever
Q48277726One novel and two uncommon MEFV mutations in Japanese patients with familial Mediterranean fever: a clinicogenetic study
Q91715174Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia
Q58703969Subclinical inflammation in a case of menstruation-induced familial Mediterranean fever: A case report
Q38714572Towards efficiency in rare disease research: what is distinctive and important?