Published in Clin Exp Rheumatol on October 27, 2006
Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*). Annu Rev Immunol (2009) 5.91
High prevalence of spondyloarthritis and ankylosing spondylitis among familial Mediterranean fever patients and their first-degree relatives: further evidence for the connection. Arthritis Res Ther (2013) 0.97
Familial Mediterranean fever: current perspectives. J Inflamm Res (2016) 0.95
Systemic arthritis in children: a review of clinical presentation and treatment. Int J Inflam (2011) 0.94
Developments in the scientific and clinical understanding of autoinflammatory disorders. Arthritis Res Ther (2009) 0.91
Familial mediterranean Fever as an emerging clinical model of atherogenesis associated with low-grade inflammation. Open Cardiovasc Med 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
Monogenic IL-1 mediated autoinflammatory and immunodeficiency syndromes: finding the right balance in response to danger signals. Clin Immunol (2010) 0.84
The association of inflammatory bowel disease and Mediterranean fever gene (MEFV) mutations in Turkish children. Dig Dis Sci (2010) 0.82
The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach. PLoS One (2013) 0.79
Update on Pyrin Functions and Mechanisms of Familial Mediterranean Fever. Front Microbiol (2016) 0.78
Discontinuing colchicine in symptomatic carriers for MEFV (Mediterranean FeVer) variants. Clin Rheumatol (2016) 0.78
The changing face of polyarteritis nodosa and necrotizing vasculitis. Nat Rev Rheumatol (2017) 0.75
The role of MEFV mutations in the concurrent disorders observed in patients with familial Mediterranean fever. Eur J Rheumatol (2016) 0.75
Familial Mediterranean fever, review of the literature. Clin Rheumatol (2017) 0.75
2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum (2013) 11.18
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness. Nat Genet (1999) 3.73
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet (1997) 3.51
Clinical features of Behçet's disease in children: an international collaborative study of 86 cases. J Pediatr (1998) 2.51
EULAR standardised operating procedures for the elaboration, evaluation, dissemination, and implementation of recommendations endorsed by the EULAR standing committees. Ann Rheum Dis (2004) 2.48
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney Int (2006) 2.39
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nat Genet (2000) 2.38
Bone scintigraphy as clue to previous torture. Lancet (1991) 2.16
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss. J Med Genet (2002) 2.11
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications. Am J Hum Genet (2000) 1.78
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations. Rheumatology (Oxford) (2006) 1.76
Risk factors for early-onset, ventilator-associated pneumonia in critical care patients: selected multiresistant versus nonresistant bacteria. Anesthesiology (2000) 1.70
Transverse-momentum and pseudorapidity distributions of charged hadrons in pp collisions at square root of s = 7 TeV. Phys Rev Lett (2010) 1.67
Prevalence of juvenile chronic arthritis and familial Mediterranean fever in Turkey: a field study. J Rheumatol (1998) 1.65
Study of the mass and spin-parity of the Higgs boson candidate via its decays to Z boson pairs. Phys Rev Lett (2013) 1.56
Predisposing factors for delirium in the surgical intensive care unit. Crit Care (2001) 1.55
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc Natl Acad Sci U S A (1998) 1.52
Influence of body mass index on outcome of the mechanically ventilated patients. Thorax (2010) 1.52
Is there a heterozygote advantage for familial Mediterranean fever carriers against tuberculosis infections: speculations remain? Clin Exp Rheumatol (2002) 1.51
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. Eur J Hum Genet (2001) 1.46
Is the Ala138Gly alteration of MEFV gene important for amyloidosis? Hum Mutat (2001) 1.40
No additive effects of inhaled iloprost and prone positioning on pulmonary hypertension and oxygenation in acute respiratory distress syndrome. Minerva Anestesiol (2012) 1.39
Association of antiphospholipid antibodies with systemic lupus erythematosus in a child presenting with chorea: a case report. Eur J Pediatr (1994) 1.38
Acute phase response and evolution of familial Mediterranean fever. Lancet (1999) 1.34
The genetic basis of autosomal dominant familial Mediterranean fever. QJM (2000) 1.29
Infantile acute hemorrhagic edema: a variant of leukocytoclastic vasculitis. Pediatr Dermatol (1995) 1.29
MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever. Hum Mutat (2000) 1.28
Pleural effusion in long-term hemodialysis patients. Transplant Proc (2007) 1.24
Measurement of the electron charge asymmetry in inclusive W production in pp collisions at sqrt[s]=7 TeV. Phys Rev Lett (2012) 1.23
Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease. Ann Rheum Dis (2008) 1.22
The significance of antineutrophil cytoplasmic antibody in microscopic polyangitis and classic polyarteritis nodosa. Arch Dis Child (2001) 1.20
Search for new physics in the multijet and missing transverse momentum final state in proton-proton collisions at √s = 7 TeV. Phys Rev Lett (2012) 1.19
Azimuthal anisotropy of charged particles at high transverse momenta in Pb-Pb collisions at sqrt[s(NN)] = 2.76 TeV. Phys Rev Lett (2012) 1.19
Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): a concomitant disease or a feature of FMF? Semin Arthritis Rheum (2001) 1.17
Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever. Clin Exp Rheumatol (2003) 1.17
Diagnostic criteria for polyarteritis nodosa in childhood. J Pediatr (1992) 1.17
MEFV mutations in Behçet's disease. Hum Mutat (2000) 1.13
E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Ann Rheum Dis (2004) 1.12
Guidelines for the genetic diagnosis of hereditary recurrent fevers. Ann Rheum Dis (2012) 1.11
Familial Mediterranean fever--renal involvement by diseases other than amyloid. Nephrol Dial Transplant (1999) 1.11
Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis. Eur J Pediatr (1997) 1.11
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis. J Med Genet (2003) 1.11
The role of cytokines in Henoch Schonlein purpura. Scand J Rheumatol (1997) 1.10
Search for a W' or techni-ρ decaying into WZ in pp Collisions at sqrt[s] = 7 TeV. Phys Rev Lett (2012) 1.10
A case of Pearson syndrome associated with multiple renal cysts. Pediatr Nephrol (1996) 1.10
Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis. Genes Immun (2004) 1.09
Search for new physics with same-sign isolated dilepton events with jets and missing transverse energy. Phys Rev Lett (2012) 1.09
Cost analysis of acute burn patients treated in a burn centre: the Gulhane experience. Ann Burns Fire Disasters (2011) 1.08
Search for supersymmetry at the LHC in events with jets and missing transverse energy. Phys Rev Lett (2011) 1.08
Search for stopped Gluinos in pp collisions at square root s=7 TeV. Phys Rev Lett (2011) 1.07
The Turkish version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ). Clin Exp Rheumatol (2001) 1.06
Measurement of the Υ1S, Υ2S, and Υ3S polarizations in pp collisions at sqrt[s] = 7 TeV. Phys Rev Lett (2013) 1.05
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34. Am J Hum Genet (1999) 1.04
Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis. Rheumatology (Oxford) (2000) 1.04
Familial Mediterranean fever and amyloidosis in children. Acta Paediatr (1993) 1.03
Giant vascular eccrine spiradenoma. Int J Dermatol (1998) 1.02
Skin test positivity to aeroallergens in the patients with chronic urticaria without allergic respiratory disease. J Investig Allergol Clin Immunol (2004) 1.02
Blood pressure nomograms for children and adolescents in Turkey. Pediatr Nephrol (1999) 1.02
Performance of the new SLICC classification criteria in childhood systemic lupus erythematosus: a multicentre study. Clin Exp Rheumatol (2014) 1.01
Renal involvement in polyarteritis nodosa: evaluation of 26 Turkish children. Pediatr Nephrol (2000) 1.00
Tumour necrosis factor alpha G-->A -238 and G-->A -308 polymorphisms in juvenile idiopathic arthritis. Rheumatology (Oxford) (2002) 0.99
Measurement of the polarization of W bosons with large transverse momenta in W + jets events at the LHC. Phys Rev Lett (2011) 0.99
Measurement of the inclusive jet cross section in pp collisions at √s = 7 TeV. Phys Rev Lett (2011) 0.98
A recruitment maneuver improves apneic oxygenation. Minerva Anestesiol (2011) 0.98
Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis. Acta Paediatr (2000) 0.98
Search for neutral minimal supersymmetric standard model Higgs bosons decaying to tau pairs in pp collisions at √s=7 TeV. Phys Rev Lett (2011) 0.97
The effects of caffeic acid phenethyl ester (CAPE) on spinal cord ischemia/reperfusion injury in rabbits. Eur J Cardiothorac Surg (1999) 0.97
Systemic oxalosis: pathognomonic renal and specific extrarenal findings on US and CT. Pediatr Radiol (1995) 0.96
Familial aggregation in Behçet's disease: high frequency in siblings and parents of pediatric probands. J Pediatr (1999) 0.95
Measurement of associated production of vector bosons and top quark-antiquark pairs in pp collisions at sqrt[s]=7 TeV. Phys Rev Lett (2013) 0.95
Search for dark matter and large extra dimensions in pp collisions yielding a photon and missing transverse energy. Phys Rev Lett (2012) 0.95
Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population. J Med Genet (1997) 0.94
In vitro chromosomal radiosensitivity in common variable immune deficiency. Clin Immunol Immunopathol (1998) 0.93
Interferon-gamma assays for the diagnosis of tuberculosis infection before using tumour necrosis factor-alpha blockers. Int J Tuberc Lung Dis (2007) 0.93
Plasma superoxide dismutase activity and malondialdehyde level correlate with the extent of acute appendicitis. Pediatr Surg Int (2000) 0.93
Familial Mediterranean fever and acute rheumatic fever: a pathogenetic relationship? Clin Rheumatol (1999) 0.92
Reliability of procalcitonin as a severity marker in critically ill patients with inflammatory response. Anaesth Intensive Care (2002) 0.92
Acrokeratoelastoidosis treated with the erbium:YAG laser. Clin Exp Dermatol (2007) 0.92
First measurement of Bose-Einstein correlations in proton-proton collisions at √s=0.9 and 2.36 TeV at the LHC. Phys Rev Lett (2010) 0.91
Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneity. Eur J Hum Genet (2000) 0.91