Published in J BUON on April 16, 2007
Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe. Hum Genet (2004) 2.21
An epidemic of silicosis among former denim sandblasters. Eur Respir J (2008) 1.78
Giant hydatid lung cysts. Eur J Cardiothorac Surg (2001) 1.56
Is the Ala138Gly alteration of MEFV gene important for amyloidosis? Hum Mutat (2001) 1.40
The management of esophagogastric anastomotic leak after esophagectomy for esophageal carcinoma. Dis Esophagus (2008) 1.40
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey. Pediatr Hematol Oncol (1996) 1.39
Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence. Eur J Haematol (1999) 1.39
Hydatid disease of rib. Ann Thorac Surg (2001) 1.26
Total intravenous anesthesia for evacuation of a hydatidiform mole and termination of pregnancy in a patient with thyrotoxicosis. Int J Obstet Anesth (2007) 1.19
Neural tube defects and Chernobyl? Paediatr Perinat Epidemiol (1989) 1.18
Differential structuring of human populations for homologous X and Y microsatellite loci. Am J Hum Genet (1997) 1.12
Beneficial effect of intracellular trehalose on the membrane integrity of dried mammalian cells. Cryobiology (2001) 1.07
Prothrombin gene 20210 G-A mutation in the Turkish population. Am J Hematol (1998) 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
Further delineation of the molecular pathology of Wilson disease in the Mediterranean population. Hum Mutat (1998) 1.03
Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa. Ann Hum Genet (2000) 1.00
Familial Mediterranean fever--amyloidosis and the Val726Ala mutation. N Engl J Med (1998) 1.00
Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis. Acta Paediatr (2000) 0.98
Beta thalassaemia mutations in the Turkish population. J Med Genet (1987) 0.96
Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations. J Med Genet (1999) 0.95
Anomalous origin of circumflex coronary artery from the right pulmonary artery associated with subaortic stenosis and coarctation of the aorta. Eur J Cardiothorac Surg (1997) 0.93
The role of prothrombotic mutations in patients with Buerger's disease. Thromb Res (2000) 0.93
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey. Eur J Pediatr (2003) 0.93
Fertilization and development of mouse oocytes cryopreserved using a theoretically optimized protocol. Hum Reprod (1996) 0.93
Epstein-Barr virus genotypes in AIDS-associated lymphomas are similar to those in endemic Burkitt's lymphomas. Leukemia (1992) 0.92
The molecular basis of beta-thalassemia in Turkey. Hum Genet (1992) 0.92
Intramural esophageal bronchogenic cysts: a review of the literature. Dis Esophagus (2007) 0.91
Genotype distribution of Candida albicans isolates by 25S intron analysis with regard to invasiveness. Mycoses (2004) 0.90
Isolated recurrent pericarditis in a patient with familial Mediterranean fever. Eur J Pediatr (2001) 0.90
Morgagni hernia: transabdominal or transthoracic approach? Acta Chir Belg (2014) 0.89
Zinc levels of serum, plasma, erythrocytes and hair in Turkish women with anencephalic babies. Prog Clin Biol Res (1983) 0.89
Plasma endothelin-1 levels in patients with left-to-right shunt with or without pulmonary hypertension. Int J Cardiol (1999) 0.88
MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis? Clin Genet (2000) 0.88
Factor V 1691 G-A mutation in children with intracardiac thrombosis: a prospective study. Acta Paediatr (2002) 0.88
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians. Hum Genet (2001) 0.88
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients. Hum Genet (1996) 0.88
Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemia. Pediatr Int (2001) 0.86
Effects of zinc supplementation on linear growth in beta-thalassemia (a new approach). Am J Hematol (1987) 0.85
Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome. Clin Exp Rheumatol (2001) 0.85
Frequency of Factor V (1691 G --> A) mutation in Turkish population. Thromb Haemost (1997) 0.85
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey. Clin Genet (2003) 0.84
Surgical treatment of mediastinal cysts: report on 29 cases. Acta Chir Belg (2012) 0.84
Evaluation of cardiac functions in patients with thalassemia major. Ann Nucl Med (1999) 0.84
A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area. Ann Hum Genet (2001) 0.84
Serum interleukin-2 and interleukin-6 levels in iron deficiency anemia. Pediatr Hematol Oncol (1998) 0.83
Detection of virulence factors of Escherichia coli from children by multiplex polymerase chain reaction. Int J Clin Pract (2006) 0.83
Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population. J Med Genet (1984) 0.83
Oesophageal adenoid cystic carcinoma and its management options. Int J Clin Pract (2005) 0.82
Thromboembolism in beta-thalassemia major. Acta Haematol (1998) 0.82
Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children. J Pediatr Endocrinol Metab (2006) 0.82
Childhood migraine and hypercoagulopathy. Br J Haematol (2011) 0.82
Total occlusion of the superior vena cava due to bronchogenic cyst. Acta Chir Belg (2009) 0.82
Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease. Heart (2002) 0.82
Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia. Clin Genet (2005) 0.81
DDAVP shortens bleeding time in Bernard-Soulier syndrome. Thromb Haemost (1994) 0.81
Serum levels of IGF-I and IGFBP-III and their relation with carcinoembryonic antigen and carbohydrate antigen 19-9 in cases of esophageal cancer. Int J Clin Pract (2006) 0.81
Vascular endothelial growth factor 936 C/T polymorphism in cancer patients. Ann Oncol (2006) 0.81
Effects of fish size on the response of antioxidant systems of Oreochromis niloticus following metal exposures. Fish Physiol Biochem (2014) 0.80
Ultrastructural changes in the mucosa of the small intestine in patients with geophagia (Prasad's syndrome). J Pediatr Gastroenterol Nutr (1990) 0.80
Hemoglobinopathies in the district of Antalya, Turkey. Pediatr Hematol Oncol (1993) 0.80
Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village. J Pediatr Endocrinol Metab (2002) 0.80
Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction. Clin Cardiol (2001) 0.80
Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients. J Pediatr Endocrinol Metab (2001) 0.80
Muco-epidermoid carcinoma of the oesophagus: a case report. Acta Chir Belg (2009) 0.79
Ethyl pyruvate protects colonic anastomosis from ischemia-reperfusion injury. Surg Innov (2008) 0.79
Zinc status in pregnancy and the occurrence of anencephaly in Turkey. J Trace Elem Electrolytes Health Dis (1988) 0.79
Localized Castleman's disease and nephrotic syndrome not responsive to resection plus colchicine therapy. Ann Hematol (2002) 0.79
Mediastinal bronchogenic cyst treated by mediastinoscopic drainage. Surg Endosc (2003) 0.78
A randomized trial of four cycles of adjuvant AC (adriamycin + cyclophosphamide) +/- two cycles of EP (etoposide + cisplatin) in node positive patients with breast cancer. Ann Oncol (2001) 0.78
Plasminogen activator inhibitor -1 gene 4G/5G polymorphism in patients with breast cancer. J BUON (2007) 0.78
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family. Clin Genet (2002) 0.78
Survival after curative resection for stage IE and IIE primary gastric lymphoma. Hepatogastroenterology (2001) 0.78
A novel 13 Bp deletion in the 3'UTR of the beta-globin gene causes beta-thalassemia in a Turkish patient. Hemoglobin (1993) 0.78
E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients. Pediatrics (2001) 0.78
Effects of calcitonin therapy on osteoporosis in patients with thalassemia. Acta Haematol (1995) 0.78
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N. Haemophilia (2006) 0.77
Deletion polymorphism of the angiotensin I converting enzyme gene is a potent risk factor for coronary artery ectasia. Heart (2003) 0.77
Maternal hair zinc concentration in neural tube defects in Turkey. Biol Trace Elem Res (1991) 0.77
Burkitt's lymphoma between African and American types in Turkish children: clinical, viral (EBV), and molecular studies. Med Pediatr Oncol (1993) 0.77
The effects of increased freshwater salinity in the biodisponibility of metals (Cr, Pb) and effects on antioxidant systems of Oreochromis niloticus. Ecotoxicol Environ Saf (2012) 0.77
Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis. Pediatr Nephrol (1995) 0.77
p53 Gene Polymorphisms in the Turkish Population. Turk J Haematol (1999) 0.77
The role of thrombophilic risk factors in the severity of pulmonary thromboembolism. Eur Respir J (2002) 0.77
Factor V Leiden and PT G20210A mutations in cancer patients with and without venous thrombosis. J Thromb Haemost (2005) 0.77
Disorders of sexual development: an overview of 18 years experience in the pediatric Endocrinology Department of Ankara University. J Pediatr Endocrinol Metab (2010) 0.77
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene. Genet Couns (2003) 0.77
Effect of zinc supplementation in a Turkish woman with two previous anencephalic infants. Gynecol Obstet Invest (1991) 0.76
Alcohol and zinc deficiency: contribution to villous atrophy. J Intern Med (1990) 0.76
Desferrioxamine and urinary zinc excretion in beta-thalassemia major. Pediatr Hematol Oncol (1993) 0.76
Recombinant human growth hormone treatment in children with thalassemia major. Pediatr Int (1999) 0.76
Carotid intima-media thickness and ACE-gene polymorphism in hemodialysis patients. J Nephrol (1999) 0.76
Interferon treatment of hepatitis B and C in beta-thalassemia. Pediatr Hematol Oncol (1995) 0.76
Further notes on neural tube defects and Chernobyl. Paediatr Perinat Epidemiol (1994) 0.76