Published in Pediatr Hematol Oncol on December 01, 1993
Rheumatological manifestations of haematological diseases. Ann Rheum Dis (1995) 0.78
Hematopoietic stem cell transplantation activity and trends at a pediatric transplantation center in Turkey during 1998-2008. Turk J Haematol (2012) 0.75
Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe. Hum Genet (2004) 2.21
Is the Ala138Gly alteration of MEFV gene important for amyloidosis? Hum Mutat (2001) 1.40
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
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey. Pediatr Hematol Oncol (1996) 1.39
Assessment of sociodemographic factors and socio-economic status affecting the coverage of compulsory and private immunization services in Istanbul, Turkey. Public Health (2005) 1.22
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
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
Resistance against contraception or medical contraceptive methods: a qualitative study on women and men in Istanbul. Eur J Contracept Reprod Health Care (2004) 1.03
Aspergillus surveillance project at a large tertiary-care hospital. J Hosp Infect (2005) 1.02
Predictors of early leaving from the cotton spinning mill environment in newly hired workers. Occup Environ Med (2006) 1.02
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
The effect of kefir on the activities of GSH-Px, GST, CAT, GSH and LPO levels in carbon tetrachloride-induced mice tissues. J Vet Med B Infect Dis Vet Public Health (2003) 0.99
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
Neonatal tumor necrosis factor, interleukin-1 alpha, interleukin-1 beta, and interleukin-6 response to infection. Am J Perinatol (1994) 0.95
Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations. J Med Genet (1999) 0.95
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey. Eur J Pediatr (2003) 0.93
The role of prothrombotic mutations in patients with Buerger's disease. Thromb Res (2000) 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
A prospective, randomized, double-blind, placebo-controlled trial of glyceryl-trinitrate ointment in the treatment of children with anal fissure. J Pediatr Surg (1999) 0.91
Predictive value of plasma and cerebrospinal fluid tumour necrosis factor-alpha and interleukin-1 beta concentrations on outcome of full term infants with hypoxic-ischaemic encephalopathy. Arch Dis Child Fetal Neonatal Ed (1998) 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
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
Lead, chromium, and cadmium exposure during abrasive blasting. Arch Environ Health (1996) 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
Rubella seroprevalence among first-grade primary school students in a district in Istanbul, Turkey. Public Health (2005) 0.85
Frequency of Factor V (1691 G --> A) mutation in Turkish population. Thromb Haemost (1997) 0.85
Cytokines in acute rheumatic fever. Eur J Pediatr (1997) 0.85
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
Magnetic resonance imaging in diagnosis of childhood central nervous system tuberculosis. Infection (2001) 0.84
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
Serum interleukin-2 and interleukin-6 levels in iron deficiency anemia. Pediatr Hematol Oncol (1998) 0.83
Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population. J Med Genet (1984) 0.83
Detection of virulence factors of Escherichia coli from children by multiplex polymerase chain reaction. Int J Clin Pract (2006) 0.83
Central diabetes insipitus in a patient with congenital toxoplasmosis. Am J Perinatol (1998) 0.83
Effect of absorbent pads containing oregano essential oil on the shelf life extension of overwrap packed chicken drumsticks stored at four degrees Celsius. Poult Sci (2009) 0.82
Childhood migraine and hypercoagulopathy. Br J Haematol (2011) 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
Echovirus 30 outbreak of aseptic meningitis in Turkey. Pediatr Infect Dis J (2000) 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
Vascular endothelial growth factor 936 C/T polymorphism in cancer patients. Ann Oncol (2006) 0.81
HLA antigens and linkage disequilibrium patterns in Turkish Behçet's patients. J Dermatol (1998) 0.80
Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients. J Pediatr Endocrinol Metab (2001) 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
Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction. Clin Cardiol (2001) 0.80
Hypopotassemic paralysis: a rare presentation of proximal renal tubular acidosis. J Child Neurol (2001) 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
Effect of intraperitoneal immunoglobulin infusion on neutrophil function in CAPD children with and without peritonitis. Adv Perit Dial (1998) 0.79
Studies on lymphocyte cell surface in ataxia-telangiectasia. Clin Exp Immunol (1985) 0.79
Zinc status in pregnancy and the occurrence of anencephaly in Turkey. J Trace Elem Electrolytes Health Dis (1988) 0.79
Plasminogen activator inhibitor-1 gene 4G/5G polymorphism in cancer patients. J BUON (2007) 0.79
E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients. Pediatrics (2001) 0.78
Plasminogen activator inhibitor -1 gene 4G/5G polymorphism in patients with breast cancer. J BUON (2007) 0.78
Effects of calcitonin therapy on osteoporosis in patients with thalassemia. Acta Haematol (1995) 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
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family. Clin Genet (2002) 0.78
Loss of nocturnal decline of blood pressure in patients with nasal polyposis. Blood Press (1999) 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
Assessment of ventricular repolarization in deaf-mute children. Pediatr Cardiol (2000) 0.77
Thrombopoietin levels of thrombocytopenic term and preterm newborns with infection. Am J Perinatol (2001) 0.77
Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis. Pediatr Nephrol (1995) 0.77
Factor V Leiden and PT G20210A mutations in cancer patients with and without venous thrombosis. J Thromb Haemost (2005) 0.77
The role of thrombophilic risk factors in the severity of pulmonary thromboembolism. Eur Respir J (2002) 0.77
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene. Genet Couns (2003) 0.77
p53 Gene Polymorphisms in the Turkish Population. Turk J Haematol (1999) 0.77
Maternal hair zinc concentration in neural tube defects in Turkey. Biol Trace Elem Res (1991) 0.77
Failure of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor in a patient with Kostmann syndrome. Turk J Pediatr (2000) 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
Deletion polymorphism of the angiotensin I converting enzyme gene is a potent risk factor for coronary artery ectasia. Heart (2003) 0.77
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
Renal functional reserve in insulin dependent diabetic children. Acta Paediatr Jpn (1998) 0.76
Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in turkish thromboembolic patients. Am J Hematol (2000) 0.76
Further notes on neural tube defects and Chernobyl. Paediatr Perinat Epidemiol (1994) 0.76
Carotid intima-media thickness and ACE-gene polymorphism in hemodialysis patients. J Nephrol (1999) 0.76
Desferrioxamine and urinary zinc excretion in beta-thalassemia major. Pediatr Hematol Oncol (1993) 0.76
Factor V (His 1299 Arg) in Turkish patients with venous thromboembolism. Am J Hematol (2000) 0.76
Interferon treatment of hepatitis B and C in beta-thalassemia. Pediatr Hematol Oncol (1995) 0.76
Tumor necrosis factor-alpha gene polymorphisms in children with multiple sclerosis. Neuropediatrics (2001) 0.76
Recombinant human growth hormone treatment in children with thalassemia major. Pediatr Int (1999) 0.76
Alcohol and zinc deficiency: contribution to villous atrophy. J Intern Med (1990) 0.76
A further case of homozygous G20210A prothrombin gene mutation without thromboembolic events. Clin Appl Thromb Hemost (1999) 0.76
Effect of zinc supplementation in a Turkish woman with two previous anencephalic infants. Gynecol Obstet Invest (1991) 0.76
Neutrophil, monocyte and lymphocyte locomotion in rheumatic fever and rheumatoid arthritis. Turk J Pediatr (1991) 0.76