Published in Arch Oral Biol on February 04, 2010
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest (2011) 2.21
Saliva and serum levels of pentraxin-3 and interleukin-1β in generalized aggressive or chronic periodontitis. J Periodontol (2013) 2.08
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
Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey. Rheumatol Int (2010) 1.51
Cervical vestibular evoked myogenic potentials in primary headache disorders. Clin Neurophysiol (2012) 1.45
Periodontal infections and pre-term low birth weight: a case-control study. J Clin Periodontol (2005) 1.39
Irrational use of antibiotics among university students. J Infect (2005) 1.39
Positive association of macrophage migration inhibitory factor gene-173G/C polymorphism with biliary atresia. J Pediatr Gastroenterol Nutr (2006) 1.13
TLR2 Arg753Gly, TLR4 Asp299Gly and Thr399Ile gene polymorphisms are not associated with chronic periodontitis in a Turkish population. J Clin Periodontol (2007) 1.04
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
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
Recovery of visual-field defects after occipital lobe infarction: a perimetric study. J Neurol Neurosurg Psychiatry (2010) 0.92
Gingival crevicular fluid transforming growth factor-beta1 in several forms of periodontal disease. Arch Oral Biol (2006) 0.91
Interleukin-10 (-1082G/A) gene polymorphism in patients with type 2 diabetes with and without nephropathy. Genet Test Mol Biomarkers (2011) 0.89
Gene polymorphisms of matrix metalloproteinase-2, -9 and -12 in periodontal health and severe chronic periodontitis. Arch Oral Biol (2007) 0.89
Periodontal therapy in chronic periodontitis lowers gingival crevicular fluid interleukin-1beta and DAS28 in rheumatoid arthritis patients. Rheumatol Int (2013) 0.88
Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome. Turk J Haematol (2015) 0.88
Accuracy and reproducibility of two manual periodontal probes. An in vitro study. J Clin Periodontol (2004) 0.85
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
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
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
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
Salivary and plasma levels of Toll-like receptor 2 and Toll-like receptor 4 in chronic periodontitis. J Periodontol (2010) 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 TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease. J 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
The effect of insulin glargine and nutritional model on metabolic control, quality of life and behavior in children and adolescents with type 1 diabetes mellitus. Acta Diabetol (2007) 0.81
TGF-beta1 gene polymorphisms in periodontal diseases. Clin Biochem (2006) 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
Is ACE gene polymorphism a risk factor for renal scarring with low-grade reflux? Pediatr Nephrol (2004) 0.81
The Fc gammaRIIa polymorphism in Turkish children with asthma bronchial and allergic rhinitis. Clin Biochem (2007) 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
Is there an interaction between polycystic ovary syndrome and gingival inflammation? J Periodontol (2012) 0.81
The progesterone receptor PROGINS polymorphism is not related to oxidative stress factors in women with polycystic ovary syndrome. Cardiovasc Diabetol (2007) 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
Salivary cytokines and the association between obstructive sleep apnea syndrome and periodontal disease. J Periodontol (2014) 0.80
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
[The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease]. Turk Kardiyol Dern Ars (2009) 0.80
The efficacy of Xialine in patients with Sjögren's syndrome: a single-blind, cross-over study. Clin Oral Investig (2007) 0.79
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
Association of the IL-1RN2 allele with periodontal diseases. Clin Biochem (2006) 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
Antimicrobial and antioxidant activities with acute toxicity, cytotoxicity and mutagenicity of Cystoseira compressa (Esper) Gerloff & Nizamuddin from the coast of Urla (Izmir, Turkey). Cytotechnology (2013) 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
Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis (2004) 0.79
Matrix metalloproteinase-2, -9, and -12 gene polymorphisms in generalized aggressive periodontitis. J Periodontol (2007) 0.79
Low-dose intravenous pamidronate treatment in osteogenesis imperfecta. Turk J Pediatr (2006) 0.79
Effects of menstrual cycle on periodontal health and gingival crevicular fluid markers. J Periodontol (2010) 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
Hypertension and ace gene insertion/deletion polymorphism in pediatric renal transplant patients. Pediatr Transplant (2005) 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
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
Renal scarring and osteopontin gene C/T polymorphism in children with primary vesicoureteral reflux. Indian Pediatr (2011) 0.78
Effect of the menstrual cycle on pain experience associated with periodontal therapy: randomized, pilot study. J Clin Periodontol (2005) 0.78
LY96, UPKIB mutations and TLR4, CD14, MBL polymorphisms in children with urinary tract infection. Indian J Pediatr (2011) 0.78
Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome. J Renin Angiotensin Aldosterone Syst (2005) 0.77
Exposure of Porphyromonas gingivalis to cortisol increases bacterial growth. Arch Oral Biol (2013) 0.77
Interleukin-33 levels in gingival crevicular fluid, saliva, or plasma do not differentiate chronic periodontitis. J Periodontol (2011) 0.77
[Familial Mediterranean fever with pulmonary manifestations alone; early diagnosis with genetic analysis]. Tuberk Toraks (2012) 0.77
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
Design and formulation of mebeverine HCl semisolid formulations for intraorally administration. AAPS PharmSciTech (2010) 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
Renin-angiotensin gene polymorphisms in relation to severe chronic periodontitis. J Clin Periodontol (2009) 0.77
Plasma levels of C-telopeptide pyridinoline cross-links of type I collagen and osteocalcin in chronic periodontitis. Inflammation (2011) 0.77
FcgammaRIIIa-V/F 158 polymorphism in Turkish children with asthma bronchiale and allergic rhinitis. Pediatr Allergy Immunol (2008) 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
Association of platelet-activating factor acetylhydrolase gene polymorphism with premature coronary artery disease in Turkish patients. Anadolu Kardiyol Derg (2006) 0.76
N-acetylcysteine in patients with COPD exacerbations associated with increased sputum. Wien Klin Wochenschr (2015) 0.76
A novel p.S34N mutation of CAMP gene in patients with periodontal disease. Arch Oral Biol (2011) 0.76
Effect of monocyte chemoattractant protein-1 (MCP-1) gene polymorphism in Turkish patients with premature coronary artery disease. Scand J Clin Lab Invest (2008) 0.76
Balance in posterior and horizontal canal type benign paroxysmal positional vertigo before and after canalith repositioning maneuvers. Gait Posture (2009) 0.76
A rare cause of chronic renal failure in a girl with elevated serum uric acid level. Pediatr Nephrol (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
SPP1 gene polymorphisms associated with nephrolithiasis in Turkish pediatric patients. Urol J (2012) 0.76
[Character and temperament dimensions of patients with temporomandibular disorder]. Turk Psikiyatri Derg (2008) 0.76
Endothelial nitric oxide synthase Glu298Asp gene polymorphism in periodontal diseases. J Periodontol (2006) 0.75
X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case report. Case Rep Med (2013) 0.75