Published in Eur J Gynaecol Oncol on January 01, 2006
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
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
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
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss. J Med Genet (2002) 2.11
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
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
Association of antiphospholipid antibodies with systemic lupus erythematosus in a child presenting with chorea: a case report. Eur J Pediatr (1994) 1.38
The significance of antineutrophil cytoplasmic antibody in microscopic polyangitis and classic polyarteritis nodosa. Arch Dis Child (2001) 1.20
Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever. Clin Exp Rheumatol (2003) 1.17
Reasons for not using family planning methods in Eastern Turkey. Eur J Contracept Reprod Health Care (2003) 1.14
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 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
Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis. Genes Immun (2004) 1.09
The Turkish version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ). Clin Exp Rheumatol (2001) 1.06
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
Familial Mediterranean fever and amyloidosis in children. Acta Paediatr (1993) 1.03
Giant vascular eccrine spiradenoma. Int J Dermatol (1998) 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
Primary giant leiomyoma of the ovary--case report. Eur J Gynaecol Oncol (2006) 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
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
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
Are carriers for MEFV mutations "healthy"? Clin Exp Rheumatol (2006) 0.92
The relationship between clinico-biochemical characteristics and psychiatric distress in young women with polycystic ovary syndrome. J Int Med Res (2008) 0.92
Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneity. Eur J Hum Genet (2000) 0.91
Three cases of verrucous carcinoma. Australas J Dermatol (1998) 0.91
MEFV mutations in systemic onset juvenile idiopathic arthritis. Rheumatology (Oxford) (2008) 0.90
Caffeic acid phenethyl ester prevents intestinal reperfusion injury in rats. J Pediatr Surg (1999) 0.90
Serum concentration and urinary excretion of beta 2-microglobulin and microalbuminuria in familial Mediterranean fever. Arch Dis Child (1994) 0.88
Plasma lipids and lipoproteins in juvenile chronic arthritis. Clin Rheumatol (1996) 0.87
Takayasu's arteritis and tuberculosis: a case report. Clin Rheumatol (2000) 0.87
Sacroiliitis in familial Mediterranean fever: an unusual presentation in childhood. Turk J Pediatr (2000) 0.86
Behçet's disease with severe arterial involvement in a child. Clin Rheumatol (2002) 0.85
Metastatic bone marrow tumours: a report of six cases and review of the literature. Haematologia (Budap) (2001) 0.85
The gingival crevicular fluid interleukin-1 beta and tumour necrosis factor-alpha levels in patients with rapidly progressive periodontitis. Aust Dent J (1995) 0.85
Assessment of occupational exposure to magnetic fields in high-voltage substations (154/34.5 kV). Radiat Prot Dosimetry (2007) 0.84
Etanercept in the treatment of arthritis in a patient with familial Mediterranean fever. Clin Exp Rheumatol (2006) 0.84
Ovarian gonodoblastoma with yolk sac tumor in a young 46, XX female: case report. Eur J Gynaecol Oncol (2007) 0.84
Caffeic acid phenethyl ester to inhibit posterior capsule opacification in rabbits. J Cataract Refract Surg (1997) 0.84
Teratoma presenting as a cystic lesion on the chest wall. Scand Cardiovasc J (2000) 0.83
Identification of Th subsets in juvenile rheumatoid arthritis confirmed by intracellular cytokine staining. J Rheumatol (1998) 0.83
Carbamazepine poisoning: treatment with plasma exchange. Hum Exp Toxicol (2001) 0.83
Efficacy of oxybutynin, pseudoephedrine and indomethacin in the treatment of primary nocturnal enuresis. Turk J Pediatr (1996) 0.82
Anxiety and depression before and after the menopause. Arch Gynecol Obstet (2001) 0.82
Nutritional assessment of children on haemodialysis: value of IGF-I, TNF-alpha and IL-1beta. Nephrol Dial Transplant (1998) 0.82
Hypercoagulopathy in a hemodialysis patient: are elevations in factors VII and VIII effective? Nephron (1999) 0.82
Current educational status of paediatric rheumatology in Europe: the results of PReS survey. Clin Exp Rheumatol (2009) 0.82
Occult parathyroid carcinoma in a patient with papillary thyroid carcinoma and Hashimoto's thyroiditis. J Endocrinol Invest (2001) 0.82
The prevalence of familial Mediterranean fever in the Turkish province of Denizli: a field study with a zero patient design. Clin Exp Rheumatol (2004) 0.81
Myelodysplastic features in juvenile rheumatoid arthritis. Am J Hematol (1997) 0.81
Myelodysplastic features in polyarteritis nodosa. Pediatr Hematol Oncol (2001) 0.81
Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritis. Arthritis Rheum (2001) 0.81
M680I(Arm2)/M694V(Med) mutations in a patient with familial Mediterranean fever and polyarteritis nodosa. Nephrol Dial Transplant (1998) 0.80
Survey of factor V leiden and prothrombin gene mutations in systemic lupus erythematosus. Clin Rheumatol (2001) 0.80
Association of sets of alleles of genes encoding beta3-adrenoreceptor, uncoupling protein 1 and lipoprotein lipase with increased risk of metabolic complications in obesity. Int J Obes Relat Metab Disord (2000) 0.80
Erdosteine ameliorates neurological outcome and oxidative stress due to ischemia/reperfusion injury in rabbit spinal cord. Eur J Vasc Endovasc Surg (2004) 0.79
Epidemiology of rheumatic heart disease. Arch Dis Child (1988) 0.79
Pyrin Q148 mutation and familial Mediterranean fever. QJM (2002) 0.79
Familial Mediterranean fever: a misnomer? Lancet (1994) 0.79
An unaddressed issue: domestic violence and unplanned pregnancies among pregnant women in Turkey. Eur J Contracept Reprod Health Care (2003) 0.79
Bone mineral density in children with familial Mediterranean fever. Clin Rheumatol (2004) 0.79
Henoch-Schönlein nephritis: a nationwide study. Nephron Clin Pract (2009) 0.79
Membranoproliferative glomerulonephritis in childhood: factors affecting prognosis. Int Urol Nephrol (1997) 0.78
Giant bladder leiomyoma presenting as a pelvic mass: a case report. Eur J Gynaecol Oncol (2007) 0.78
C reactive protein: protecting from lupus in familial Mediterranean fever. Ann Rheum Dis (2005) 0.78
Anaemia in juvenile chronic arthritis. Clin Rheumatol (1996) 0.78
GnRH agonist decreases endothelial nitric oxide synthase (eNOS) expression in leiomyoma. Int J Gynaecol Obstet (2000) 0.78
Plasma atrial natriuretic peptide and endothelin levels in acute poststreptococcal glomerulonephritis. Pediatr Nephrol (1992) 0.78
The role of apoptosis in childhood Henoch-Schonlein purpura. Clin Rheumatol (2003) 0.77
Eight years' experience of uterine rupture cases. J Obstet Gynaecol (2005) 0.77
The analysis of interleukin-1 receptor antagonist and interleukin-1beta gene polymorphisms in Turkish FMF patients: do they predispose to secondary amyloidosis? Clin Exp Rheumatol (2008) 0.77
The triad of weight loss, fever and night sweating: isolated bone marrow tuberculosis, a case report. J Chemother (2002) 0.77
Interferon-alpha-induced mood disorder with manic features. Gen Hosp Psychiatry (2001) 0.77
The impact of physical and psychological comorbid conditions on the quality of life of patients with acute myocardial infarction: a multi-center, cross-sectional observational study from Turkey. Int J Psychiatry Med (2013) 0.77
Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children. Lupus (2012) 0.77
Successful treatment of polyarteritis nodosa with interferon alpha in a nine-month old girl. Eur J Pediatr (2001) 0.77
Maternal serum ceruloplasmin in preeclampsia. Int J Gynaecol Obstet (2005) 0.77
Antineutrophil cytoplasmic antibodies in childhood systemic lupus erythematosus. Clin Rheumatol (1998) 0.77
A case of familial Mediterranean fever, Behçet's disease and polyarteritis nodosa complicated by perirenal haematoma. Clin Exp Rheumatol (2001) 0.77
Evaluation of tumour necrosis factor alpha, interferon gamma and granulocyte-macrophage colony stimulating factor levels in juvenile chronic arthritis. Rheumatology (Oxford) (1999) 0.76
Rectal cancer and pregnancy: report of two cases. Eur J Gynaecol Oncol (2009) 0.76
Serum trace elements and heavy metals in polycystic ovary syndrome. Hum Exp Toxicol (2011) 0.76
Preimplantation genetic diagnosis for early-onset torsion dystonia. Reprod Biomed Online (2004) 0.76