Published in J Rheumatol on January 01, 2003
Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey. Rheumatol Int (2010) 1.51
Chronic inflammation in FMF: markers, risk factors, outcomes and therapy. Nat Rev Rheumatol (2010) 1.45
The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation. Nat Immunol (2017) 1.38
A rare cause of refractory ascites in a child: familial Mediterranean fever. Rheumatol Int (2009) 1.38
The clinical and genetical features of 124 children with Familial Mediterranean fever: experience of a single tertiary center. Rheumatol Int (2008) 0.96
Coexistence of vasculitides with familial Mediterranean fever. Rheumatol Int (2011) 0.91
Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey. Clin Rheumatol (2011) 0.90
Familial mediterranean Fever: a retrospective clinical and molecular study in the East of anatolia region of Turkey. Open Rheumatol J (2010) 0.87
The myths we believed in familial Mediterranean fever: what have we learned in the past years? Semin Immunopathol (2015) 0.85
Familial Mediterranean fever: genotype-phenotype correlations in Japanese patients. Medicine (Baltimore) (2014) 0.84
Familial mediterranean Fever: diagnosing as early as 3 months of age. Case Rep Pediatr (2014) 0.82
Application of the new pediatric criteria and Tel Hashomer criteria in heterozygous patients with clinical features of FMF. Eur J Pediatr (2011) 0.82
Demographic, clinical and mutational characteristics of Turkish familial Mediterranean fever patients: results of a single center in Central Anatolia. Rheumatol Int (2009) 0.81
Relationship between genetic mutation variations and acute-phase reactants in the attack-free period of children diagnosed with familial Mediterranean fever. Braz J Med Biol Res (2013) 0.79
Familial Mediterranean fever without MEFV mutations: a case-control study. Orphanet J Rare Dis (2015) 0.77
Acquired familial Mediterranean fever associated with a somatic MEFV mutation in a patient with JAK2 associated post-polycythemia myelofibrosis. Orphanet J Rare Dis (2015) 0.75
Familial Mediterranean Fever: Recent Developments in Pathogenesis and New Recommendations for Management. Front Immunol (2017) 0.75
Evaluation of the Mean Platelet Volume and Red Cell Distribution Width in FMF: Are They Related to Subclinical Inflammation or Not? Int J Chronic Dis (2014) 0.75
[Autoinflammatory diseases in childhood]. Z Rheumatol (2009) 0.75
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med (2014) 4.70
Eprodisate for the treatment of renal disease in AA amyloidosis. N Engl J Med (2007) 3.38
Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever. Arthritis Rheum (2007) 2.56
A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family. Am J Hum Genet (2002) 1.90
Clinical disease among patients heterozygous for familial Mediterranean fever. Arthritis Rheum (2009) 1.89
Biochemical subtyping of amyloid in formalin-fixed tissue samples confirms and supplements immunohistologic data. Am J Clin Pathol (2004) 1.77
Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classification. J Am Soc Nephrol (2002) 1.73
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts. Invest Ophthalmol Vis Sci (2004) 1.70
Expansion of gammadelta T-cells in Behçet's disease: role of disease activity and microbial flora in oral ulcers. J Lab Clin Med (2003) 1.69
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews. J Cardiovasc Electrophysiol (2010) 1.60
Arthritis as the sole episodic manifestation of familial Mediterranean fever. J Rheumatol (2005) 1.56
Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia. Circulation (2007) 1.55
Hydroxychloroquine: from malaria to autoimmunity. Clin Rev Allergy Immunol (2012) 1.53
Familial Mediterranean fever (FMF) with proteinuria: clinical features, histology, predictors, and prognosis in a cohort of 25 patients. J Rheumatol (2013) 1.49
The structural effect of the E148Q MEFV mutation on the pyrin protein: a study using a quantum chemistry model. Isr Med Assoc J (2011) 1.49
Familial Mediterranean fever in Ashkenazi Jews: the mild end of the clinical spectrum. J Rheumatol (2009) 1.45
Chronic inflammation in FMF: markers, risk factors, outcomes and therapy. Nat Rev Rheumatol (2010) 1.45
Raft lipids as common components of human extracellular amyloid fibrils. Proc Natl Acad Sci U S A (2005) 1.38
Clinical evidence for utilization of the A3 adenosine receptor as a target to treat rheumatoid arthritis: data from a phase II clinical trial. J Rheumatol (2007) 1.38
Evaluation of disease severity in familial Mediterranean fever. Semin Arthritis Rheum (2005) 1.34
An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis. J Invest Dermatol (2006) 1.33
Cone-rod dystrophy and a frameshift mutation in the PROM1 gene. Mol Vis (2009) 1.32
Vitamin D and autoimmune thyroid diseases. Cell Mol Immunol (2011) 1.28
Mutations in FYCO1 cause autosomal-recessive congenital cataracts. Am J Hum Genet (2011) 1.26
The infectious etiology of vasculitis. Autoimmunity (2009) 1.16
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome. Am J Hum Genet (2008) 1.14
Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. Am J Hum Genet (2002) 1.14
Collaboration in response to disaster--Typhoon Yolanda and an integrative model. N Engl J Med (2014) 1.12
Abdominal and digestive system associations of familial Mediterranean fever. Am J Gastroenterol (2003) 1.11
The contribution of genotypes at the MEFV and SAA1 loci to amyloidosis and disease severity in patients with familial Mediterranean fever. Arthritis Rheum (2003) 1.09
A missense mutation in the CASQ2 gene is associated with autosomal-recessive catecholamine-induced polymorphic ventricular tachycardia. Trends Cardiovasc Med (2003) 1.08
An antibody profile of systemic lupus erythematosus detected by antigen microarray. Immunology (2010) 1.08
Long-term outcomes in difficult-to-treat patients with recurrent pericarditis. Am J Cardiol (2006) 1.07
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nat Genet (2003) 1.07
Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron (2013) 1.06
Intravenous immunoglobulin modulates cutaneous involvement and reduces skin fibrosis in systemic sclerosis: an open-label study. Arthritis Rheum (2004) 1.05
The familial Mediterranean fever (MEVF) gene as a modifier of Crohn's disease. Am J Gastroenterol (2005) 1.05
Hearing loss as the presenting feature of systemic vasculitis. Ann N Y Acad Sci (2007) 1.01
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis. Am J Hum Genet (2012) 0.99
Familial Mediterranean fever successfully treated with etanercept. J Clin Rheumatol (2007) 0.98
Colchicine nonresponsiveness in familial Mediterranean fever: clinical, genetic, pharmacokinetic, and socioeconomic characterization. Semin Arthritis Rheum (2004) 0.98
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever. Eur J Hum Genet (2002) 0.97
The role of infection in inflammatory bowel disease: initiation, exacerbation and protection. Isr Med Assoc J (2009) 0.97
Familial Mediterranean Fever in the first two years of life: a unique phenotype of disease in evolution. J Pediatr (2010) 0.96
Analysis of the three most common MEFV mutations in 412 patients with familial Mediterranean fever. Isr Med Assoc J (2003) 0.95
The composition of normal pericardial fluid and its implications for diagnosing pericardial effusions. Am J Med (2005) 0.95
Methotrexate enhances the anti-inflammatory effect of CF101 via up-regulation of the A3 adenosine receptor expression. Arthritis Res Ther (2006) 0.95
Confirmation of the association between male pattern baldness and the androgen receptor gene. Eur J Dermatol (2005) 0.95
Male sex coupled with articular manifestations cause a 4-fold increase in susceptibility to amyloidosis in patients with familial Mediterranean fever homozygous for the M694V-MEFV mutation. J Rheumatol (2003) 0.95
A single testing of serum amyloid a levels as a tool for diagnosis and treatment dilemmas in familial Mediterranean fever. Semin Arthritis Rheum (2007) 0.94
Sarcoidosis presenting as "corset-like" myelopathy: a description of six cases and literature review. Clin Rev Allergy Immunol (2010) 0.94
Crohn disease in patients with familial Mediterranean fever. Medicine (Baltimore) (2002) 0.94
Evidence-based recommendations for the practical management of Familial Mediterranean Fever. Semin Arthritis Rheum (2013) 0.93
A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Ann Med (2004) 0.93
Incomplete response to colchicine in M694V homozygote FMF patients. Autoimmun Rev (2012) 0.93
Role of the pyrin M694V (A2080G) allele in acute myocardial infarction and longevity: a study in the Sicilian population. J Leukoc Biol (2005) 0.92
The mosaic of autoimmunity: hormonal and environmental factors involved in autoimmune diseases--2008. Isr Med Assoc J (2008) 0.92
Familial Mediterranean fever in children presenting with attacks of fever alone. J Rheumatol (2010) 0.91
Interferon-alpha as a treatment modality for colchicine- resistant familial Mediterranean fever. J Rheumatol (2008) 0.91
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24. Invest Ophthalmol Vis Sci (2006) 0.91
Response of vasculitic peripheral neuropathy to intravenous immunoglobulin. Ann N Y Acad Sci (2005) 0.90
Immunoglobulin free light chain dimers in human diseases. ScientificWorldJournal (2011) 0.90
The mosaic of autoimmunity: genetic factors involved in autoimmune diseases--2008. Isr Med Assoc J (2008) 0.90
Infectious serologies and autoantibodies in inflammatory bowel disease: insinuations at a true pathogenic role. Ann N Y Acad Sci (2009) 0.90
Large symptomatic pericardial effusion as the presentation of unrecognized cancer: a study in 173 consecutive patients undergoing pericardiocentesis. Medicine (Baltimore) (2006) 0.90
The sense of smell in systemic lupus erythematosus. Arthritis Rheum (2009) 0.89
A novel overlap syndrome: systemic sclerosis associated with antiphospholipid syndrome--a case series. Ann N Y Acad Sci (2007) 0.89
The familial Mediterranean fever gene as a modifier of periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome. Semin Arthritis Rheum (2010) 0.89
Infectious serologies and autoantibodies in Wegener's granulomatosis and other vasculitides: novel associations disclosed using the Rad BioPlex 2200. Ann N Y Acad Sci (2009) 0.89
Mortality risk factors associated with familial Mediterranean fever among a cohort of 1.25 million adolescents. Ann Rheum Dis (2013) 0.89
Charge differences between in vivo deposits in immunoglobulin light chain amyloidosis and non-amyloid light chain deposition disease. Br J Haematol (2007) 0.89
Chronic idiopathic granulomatous mastitis. Ann N Y Acad Sci (2007) 0.88
Diagnostic performance of amyloid A protein quantification in fat tissue of patients with clinical AA amyloidosis. Amyloid (2007) 0.87
Long-term therapy with intravenous immunoglobulin is beneficial in patients with autoimmune diseases. Clin Rev Allergy Immunol (2012) 0.87
Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews. Hum Genet (2002) 0.87
Risk factors for amyloidosis and impact of kidney transplantation on the course of familial Mediterranean fever. Isr Med Assoc J (2012) 0.87