Published in J Inherit Metab Dis on January 01, 1990
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Factors affecting post-operative mortality in malignant biliary tract obstruction. Hepatogastroenterology (1999) 0.86
Novel mutations cause biotinidase deficiency in Turkish children. J Inherit Metab Dis (2000) 0.86
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Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families. Clin Genet (1989) 0.85
Newborn PKU screening in Turkey: at present and organization for future. Turk J Pediatr (2001) 0.85
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Effect of vitamin E treatment on the oxidative damage occurring in Henoch-Schönlein purpura. Acta Paediatr (2003) 0.82
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Acute rheumatic fever in children in the Ankara area in 1990-1992 and comparison with a previous study in 1980-1989. Acta Paediatr (1994) 0.81
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Renal hydatid cyst detected in a child during the course of acute poststreptococcal glomerulonephritis. Nephron (1995) 0.80
Ruptured ectopic pregnancy with undetectable beta-hCG levels coexisting with acute appendicitis. Acta Obstet Gynecol Scand (1997) 0.79
Post-streptococcal acute glomerulonephritis in Turkey. Acta Paediatr (1995) 0.79
Liver pathology in transient neonatal hyperammonemia. Virchows Arch A Pathol Anat Histopathol (1983) 0.79
Propionacidaemia and immunodeficiency. Lancet (1980) 0.79
Dependence of the utilization of a phenylalanine-free amino acid mixture on different amounts of single dose ingested. A case report. Eur J Pediatr (1994) 0.78
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Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations. Hum Hered (2000) 0.78
HFE gene mutation and transferrin saturation in very low birthweight infants. Arch Dis Child Fetal Neonatal Ed (1999) 0.77
Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduria. J Inherit Metab Dis (2009) 0.77
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Use of the Static Granular Bed Reactor (SGBR) with anaerobic sludge to treat poultry slaughterhouse wastewater and kinetic modeling. Bioresour Technol (2009) 0.77
D-glyceric aciduria in a six-month-old boy presenting with West syndrome and autistic behaviour. Neuropediatrics (2002) 0.76
Infantile spasms as the initial symptom of biotinidase deficiency. J Pediatr (1994) 0.76
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A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene. JIMD Rep (2011) 0.76
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Autologous skin graft, human dura mater and polypropylene mesh for the repair of ventral abdominal hernias: an experimental study. Eur J Surg (1999) 0.76
[Phenylalanine-free amino acid mixture: metabolic effects in relation to a single dose]. Monatsschr Kinderheilkd (1991) 0.75
Congenital rickets. Eur J Pediatr (1996) 0.75
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[A simple method for diagnosis of galactosemia and its heterozygotic gene carriers]. Monatsschr Kinderheilkd (1970) 0.75
Periampullary carcinoma detected after sphincterotomy. Hepatogastroenterology (1997) 0.75
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[Comparative determination of syphilis-specific antibodies in the blood of newborn infants in various regions of West Germany]. Offentl Gesundheitswes (1982) 0.75
Papillary fibroelastoma of the ascending aorta presenting with cardiogenic shock. Minerva Cardioangiol (2006) 0.75
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Penylalanine hydroxylation in phenylketonuria. Lancet (1976) 0.75
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Gastroenteropancreatic neuroendocrine tumours contain a common set of synaptic vesicle proteins and amino acid neurotransmitters. Eur J Cancer (1993) 0.75
Effects of alpha-tocopherol on reperfusion injury in the canine small bowel autotransplantation model. Transplant Proc (1998) 0.75
A Turkish case with molybdenum cofactor deficiency. Nucleosides Nucleotides Nucleic Acids (2006) 0.75
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Fatal outcome of infantile oxalosis: case reports from three families and a review of literature. Turk J Pediatr (1998) 0.75
[Thin layer chromatographic test for the indirect and direct detection of the enzyme defect in histidinemia]. Monatsschr Kinderheilkd (1983) 0.75
Glutaraldehyde mediated echinocyte/discocyte transformation is Ca2+ dependent. Folia Haematol Int Mag Klin Morphol Blutforsch (1978) 0.75
[Free amino acids in the skeletal muscles, blood and urine of healthy persons and of patients with progressive muscular dystrophy]. Monatsschr Kinderheilkd (1967) 0.75
Hypotonic unmasking of erythrocyte receptor sites. Exp Pathol (Jena) (1979) 0.75
[Drug influence on screening tests for inborn errors of metabolism]. Monatsschr Kinderheilkd (1973) 0.75
Spread of HIV infection in the general population in Germany. AIDS (2000) 0.75
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[Screening of newborns]. Dtsch Krankenpflegez (1993) 0.75
A family with hyperimmunoglobulin M syndrome and systemic amyloidosis. Nephrol Dial Transplant (2000) 0.75
Hyperimmunoglobulin M syndrome associated with systemic amyloidosis type AA. Eur J Pediatr (1995) 0.75
[A simple method to shorten the freeze drying time]. Z Klin Chem Klin Biochem (1967) 0.75
Acute pancreatitis in a patient with partial lipodystrophy and membranoproliferative glomerulonephritis. Nephrol Dial Transplant (2001) 0.75
Plasma taurine levels in healthy cats and cats with cardiac disorders. J Nutr (1991) 0.75
Effects of ammonia on pentylenetetrazole-induced seizure threshold. Metab Brain Dis (1999) 0.75
Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis. Eur J Pediatr (1993) 0.75
Genotype-phenotype correlation in dihydropteridine reductase deficiency. J Inherit Metab Dis (2000) 0.75
[Pepper type neuroblastoma with homocystinuria. Diagnosis, biochemistry and therapy]. Helv Paediatr Acta (1970) 0.75
A case with nephrophthisis complex or a variant of the disease. Nephron (1995) 0.75
Design of a prospective neonatal cohort study of homozygous and double heterozygous factor V Leiden and factor II G20210A. Klin Padiatr (2000) 0.75