Published in Rheumatol Int on March 09, 2010
A Case of Henoch-Schönlein Purpura with P369S Mutation in MEFV Gene. Iran J Pediatr (2011) 0.86
Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations. Arthritis Res Ther (2014) 0.84
The MEFV gene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population. Balkan J Med Genet (2017) 0.75
Myalgia as a symptom of familial Mediterranean fever in children. Rheumatol Int (2011) 0.75
Relationship between clinical findings and genetic mutations in patients with familial Mediterranean fever. Pediatr Rheumatol Online J (2015) 0.75
Molecular evaluation of 458 patients referred with a clinical diagnosis of familial Mediterranean fever in Scandinavia. Rheumatol Int (2010) 0.75
Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium. Cell (1997) 7.43
A candidate gene for familial Mediterranean fever. Nat Genet (1997) 7.17
Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med (1967) 5.88
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore) (2005) 3.01
The arthritis of familial Mediterranean fever (FMF). Arthritis Rheum (1966) 2.32
Colchicine in the prevention and treatment of the amyloidosis of familial Mediterranean fever. N Engl J Med (1986) 2.29
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. Eur J Hum Genet (2001) 1.46
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications. Am J Hum Genet (1999) 1.44
Familial Mediterranean fever in children: the expanded clinical profile. QJM (1999) 1.30
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. Eur J Hum Genet (1999) 1.23
Familial Mediterranean fever: clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients. Pediatrics (1999) 1.21
Clinical versus genetic diagnosis of familial Mediterranean fever. QJM (2000) 1.17
Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF). Eur J Hum Genet (1998) 1.13
Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis. Rheumatology (Oxford) (2000) 1.04
Clinical and diagnostic value of genetic testing in 216 Israeli children with Familial Mediterranean fever. J Rheumatol (2003) 1.03
Genotype-phenotype assessment of common genotypes among patients with familial Mediterranean fever. J Rheumatol (2000) 0.98
Colchicine treatment of AA amyloidosis of familial Mediterranean fever. An analysis of factors affecting outcome. Arthritis Rheum (1994) 0.98
Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlation. Eur J Med Genet (2006) 0.94
Auto-inflammatory fever syndromes. Rheum Dis Clin North Am (2007) 0.91
Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients. Hum Mutat (2000) 0.91
Phenotype-genotype correlation in 91 patients with familial Mediterranean fever reveals a high frequency of cutaneomucous features. Rheumatology (Oxford) (2000) 0.90
The musculoskeletal manifestations of familial Mediterranean fever in children genetically diagnosed with the disease. Arthritis Rheum (2001) 0.89
Familial Mediterranean fever clinical and genetic features in Druzes and in Iraqi Jews: a preliminary study. J Rheumatol (1998) 0.77
Familial Mediterranean fever in children. J Rheumatol Suppl (1992) 0.77
MEFV mutations in Tunisian patients suffering from familial Mediterranean fever. Semin Arthritis Rheum (2007) 0.77
Strict blood-pressure control and progression of renal failure in children. N Engl J Med (2009) 5.71
Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study. J Am Soc Nephrol (2006) 2.89
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest (2011) 2.21
Insulin-like growth factor attenuates apoptosis and mucosal damage in hypoxia/reoxygenation-induced intestinal injury. Biol Neonate (2004) 1.59
Alterations of blood pressure in type 1 diabetic children and adolescents. Pediatr Nephrol (2006) 1.56
Are small residual stone fragments really insignificant in children? J Pediatr Surg (2013) 1.46
Complications of central venous catheterization in critically ill children. Pediatr Int (2007) 1.38
Genetic screening in adolescents with steroid-resistant nephrotic syndrome. Kidney Int (2013) 1.21
The Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) study: objectives, design, and methodology. Clin J Am Soc Nephrol (2010) 1.21
Quality of life in children with chronic kidney disease (with child and parent assessments). Pediatr Nephrol (2010) 1.20
Positive association of macrophage migration inhibitory factor gene-173G/C polymorphism with biliary atresia. J Pediatr Gastroenterol Nutr (2006) 1.13
The oral health status of children undergoing hemodialysis treatment. Turk J Pediatr (2003) 1.11
Reno-vascular hypertension in childhood: a nationwide survey. Pediatr Nephrol (2007) 1.03
Childhood vasculitides in Turkey: a nationwide survey. Clin Rheumatol (2006) 1.01
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. Pediatr Nephrol (2007) 0.99
G protein beta3 subunit gene polymorphism in Turkish hypertensives. Anadolu Kardiyol Derg (2008) 0.98
TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome. Nephrol Dial Transplant (2011) 0.96
Clinical outcome in children with Henoch-Schönlein nephritis. Pediatr Nephrol (2006) 0.93
Polymorphisms of the ICAM-1 gene are associated with biliary atresia. Dig Dis Sci (2008) 0.92
The G894T polymorphism on endothelial nitric oxide synthase gene is associated with premature coronary artery disease in a Turkish population. Thromb Res (2005) 0.92
Gingival crevicular fluid transforming growth factor-beta1 in several forms of periodontal disease. Arch Oral Biol (2006) 0.91
Autopsy findings of a case with oxalosis. Pediatr Dev Pathol (2009) 0.89
Gene polymorphisms of matrix metalloproteinase-2, -9 and -12 in periodontal health and severe chronic periodontitis. Arch Oral Biol (2007) 0.89
Interleukin-10 (-1082G/A) gene polymorphism in patients with type 2 diabetes with and without nephropathy. Genet Test Mol Biomarkers (2011) 0.89
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet (2011) 0.88
Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome. Turk J Haematol (2015) 0.88
Supraventricular tachycardia following insertion of a central venous catheter. Saudi J Kidney Dis Transpl (2009) 0.88
Association of macrophage migration inhibitory factor -173C allele polymorphism with steroid resistance in children with nephrotic syndrome. Pediatr Nephrol (2005) 0.86
No association of interleukin-6 gene polymorphism (-174 G/C) with premature coronary artery disease in a Turkish cohort. Coron Artery Dis (2007) 0.85
An infant with Imersland-Gräsbeck syndrome. Saudi J Kidney Dis Transpl (2012) 0.84
Macrophage migration inhibitory factor expression and MIF gene -173 G/C polymorphism in nonalcoholic fatty liver disease. Eur J Gastroenterol Hepatol (2010) 0.84
Toll-like receptor 2 and 4 gene polymorphisms in generalized aggressive periodontitis. J Periodontol (2007) 0.84
Gingival crevicular fluid EMAP-II, MIP-1alpha and MIP-1beta levels of patients with periodontal disease. J Clin Periodontol (2005) 0.84
Association between the ACE I/D gene polymorphism and physical performance in a homogeneous non-elite cohort. Can J Appl Physiol (2005) 0.84
ACE gene insertion/deletion polymorphism in childhood idiopathic nephrotic syndrome. Pediatr Nephrol (2005) 0.83
4G/5G polymorphism of PAI-1 gene and Alu-repeat I/D polymorphism of TPA gene in Turkish patients with polycystic ovary syndrome. J Assist Reprod Genet (2007) 0.83
Association of interleukin-6 -174 G>C promoter polymorphism with increased risk of type 2 diabetes mellitus patients with diabetic nephropathy in Turkey. Genet Test Mol Biomarkers (2013) 0.83
The early cardiovascular changes in pediatric patients with systemic lupus erythematosus. Pediatr Nephrol (2012) 0.83
Allelic frequency of the MCP-1 promoter -2518 polymorphism in the Turkish population and in Turkish patients with juvenile rheumatoid arthritis. Clin Rheumatol (2006) 0.82
Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections. Biochem Genet (2007) 0.82
Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease. J Rheumatol (2006) 0.82
The long-term results of pediatric patients with primary focal and segmental glomerulosclerosis. Saudi J Kidney Dis Transpl (2010) 0.82
TGF-beta1 gene polymorphisms in periodontal diseases. Clin Biochem (2006) 0.81
Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency. Ital J Pediatr (2012) 0.81
A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation. Indian J Pediatr (2008) 0.81
The Fc gammaRIIa polymorphism in Turkish children with asthma bronchial and allergic rhinitis. Clin Biochem (2007) 0.81
Effect of MMP-1 promoter polymorphisms on GCF MMP-1 levels and outcome of periodontal therapy in patients with severe chronic periodontitis. J Clin Periodontol (2008) 0.81
Efficacy of interleukin-1 targeting treatments in patients with familial mediterranean Fever. Inflammation (2015) 0.81
Is ACE gene polymorphism a risk factor for renal scarring with low-grade reflux? Pediatr Nephrol (2004) 0.81
Fas, Fas Ligand, and vitamin D Receptor FokI gene polymorphisms in patients with type 1 diabetes mellitus in the Aegean region of Turkey. Genet Test Mol Biomarkers (2012) 0.80
Lead exposure and urinary N-acetyl beta D glucosaminidase activity in adolescent workers in auto repair workshops. J Adolesc Health (2002) 0.80
[The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease]. Turk Kardiyol Dern Ars (2009) 0.80
Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. J Clin Immunol (2012) 0.80
The progesterone receptor PROGINS polymorphism is not related to oxidative stress factors in women with polycystic ovary syndrome. Cardiovasc Diabetol (2007) 0.80
A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree. J Pediatr Endocrinol Metab (2013) 0.79
Renin-angiotensin system gene polymorphisms and premature coronary heart disease. J Renin Angiotensin Aldosterone Syst (2005) 0.79
Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis (2004) 0.79
Mcp-1, eNOS, tPA and PAI-1 gene polymorphism and correlation of genotypes and phenotypes in hepatopulmonary syndrome. Dig Dis Sci (2007) 0.79
Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation. J Pediatr Endocrinol Metab (2012) 0.79
Tissue plasminogen activator and plasminogen activator inhibitor-1 gene polymorphisms in patients with chronic periodontitis. J Periodontol (2007) 0.79
Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients. Cytokine (2013) 0.79
Matrix metalloproteinase-2, -9, and -12 gene polymorphisms in generalized aggressive periodontitis. J Periodontol (2007) 0.79
Hypertension and ace gene insertion/deletion polymorphism in pediatric renal transplant patients. Pediatr Transplant (2005) 0.78
Cardiovascular functional and structural changes in children with primary hypertension. Minerva Pediatr (2014) 0.78
Hypercoagulability risk factors in children with minimal change disease and the protective role of protein-C activity. Int Urol Nephrol (2004) 0.78
LY96, UPKIB mutations and TLR4, CD14, MBL polymorphisms in children with urinary tract infection. Indian J Pediatr (2011) 0.78
Growth impairment and nutritional status in children with chronic kidney disease. Iran J Pediatr (2011) 0.78
Determination of the effects of alcohol dehydrogenase (ADH) 1B and ADH1C polymorphisms on alcohol dependence in Turkey. Sci Justice (2011) 0.78
Gene polymorphisms of tissue plasminogen activator and plasminogen activator inhibitor-1 in Turkish patients with generalized aggressive periodontitis. J Clin Periodontol (2007) 0.78
Matrix metalloproteinase (MMP)-8 and tissue inhibitor of MMP-1 (TIMP-1) gene polymorphisms in generalized aggressive periodontitis: gingival crevicular fluid MMP-8 and TIMP-1 levels and outcome of periodontal therapy. J Periodontol (2013) 0.78
Renal scarring and osteopontin gene C/T polymorphism in children with primary vesicoureteral reflux. Indian Pediatr (2011) 0.78
Gene locus ambiguity in posterior urethral valves/prune-belly syndrome. Pediatr Nephrol (2005) 0.78
MMP-13 promoter polymorphisms in patients with chronic periodontitis: effects on GCF MMP-13 levels and outcome of periodontal therapy. J Clin Periodontol (2009) 0.77
[Familial Mediterranean fever with pulmonary manifestations alone; early diagnosis with genetic analysis]. Tuberk Toraks (2012) 0.77
Renin-angiotensin gene polymorphisms in relation to severe chronic periodontitis. J Clin Periodontol (2009) 0.77
Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case report. Ren Fail (2014) 0.77
Rapidly progressive glomerulonephritis in a child with Henoch-Schönlein Vasculitis and familial Mediterranean fever. Pediatr Rheumatol Online J (2009) 0.77
FcgammaRIIIa-V/F 158 polymorphism in Turkish children with asthma bronchiale and allergic rhinitis. Pediatr Allergy Immunol (2008) 0.77
Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome. J Renin Angiotensin Aldosterone Syst (2005) 0.77
The place of androgen receptor gene mutation analysis in the molecular diagnosis of prostate cancer and genotype-phenotype relationship. Turk J Med Sci (2014) 0.77
Interleukin 8 gene 2767 A/G polymorphism is associated with increased risk of nephritis in children with Henoch-Schönlein purpura. Rheumatol Int (2011) 0.76
A very rare cause of childhood paraparesis: primary intradural extramedullary spinal hydatid cyst. Pediatr Infect Dis J (2009) 0.76
Angiotensin-converting enzyme (ACE), angiotensinogen (AGT), and angiotensin II type 1 receptor (AT1R) gene polymorphisms in generalized aggressive periodontitis. Arch Oral Biol (2009) 0.76
A novel p.S34N mutation of CAMP gene in patients with periodontal disease. Arch Oral Biol (2011) 0.76