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Determination of Physiological Indices and Some Antioxidant Enzymes of Chard Exposed to Nitric Oxide under Drought Stress
This research was carried out to determine effectiveness of nitric oxide (NO) on some physiological and biochemical reactions, and water use efficiency (WUE) of chard (Beta vulgaris L. var. cicla) under well-wate...
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Article
The IL-1RN and IL-4 gene polymorphisms are potential genetic markers of susceptibility to bladder cancer: a case–control study
We investigated the relationship between the distribution of the IL-1RN, TNF-β and IL-4 polymorphism and the clinical features of bladder cancer.
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Article
Spectrum of Brevundimonas vesicularis infections in neonatal period: a case series at a tertiary referral center
To report infections caused by Brevundimonas vesicularis and the treatment regimens administered based on antibiotic studies of this Gram-negative bacterium in the neonatal period.
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Identification of Mutations and Evaluation of Cardiomyopathy in Turkish Patients with Primary Carnitine Deficiency
Primary systemic carnitine deficiency (SCD) is an autosomal recessive disorder caused by defective cellular carnitine transport. Patients usually present with predominant metabolic or cardiac manifestations. S...
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A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene
Acrodermatitis enteropathica (AE) is a rare autosomal recessive disorder of zinc deficiency due to an abnormal intestinal zinc transporter. It is characterized by the triad of acral dermatitis, alopecia, and d...
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Mutation Spectrum of Fumarylacetoacetase Gene and Clinical Aspects of Tyrosinemia Type I Disease
Tyrosinemia type I (OMIM 276700) is a rare, autosomal recessive disorder caused by a deficiency in the fumarylacetoacetate hydrolase (FAH) enzyme. This study examined the spectrum of FAH gene mutation in 32 patie...
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Article
1279 A Nested Case-Control Study for Risk Factors of Infantile Colic
Backgroud and aims: To analyse infantile (birth characteristics, feeding type) and environmental (maternal smoking, nutrition and psychological status, mother-child bonding, family structure, support to mother...
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Article
Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency
The pyruvate dehydrogenase (PDH) complex is a mitochondrial multienzyme that catalyses the irreversible oxidative decarboxylation of pyruvate to acetyl-CoA. We report four novel PDHA1 mutations in patients with p...
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Article
Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria?
The aim of this study was to compare the level of maternal knowledge and the blood phenylalanine (Phe) control in phenylketonuria (PKU; OMIM 261600). The study was conducted on 144 children (81 boys, 63 girls)...
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Article
Neurocutaneous melanosis associated with Dandy-Walker malformation
Neurocutaneous melanosis is an uncommon congenital disorder consisting of benign or malignant melanocytic tumors of the leptomeninges with large or numerous cutaneous congenital melanocytic nevi. The Dandy-Wal...
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Article
Detection ofCandida albicans by culture, serology and PCR in clinical specimens from patients with ulcerative colitis: Re-evaluation of an old hypothesis with a new perspective
The relationship between inflammatory bowel disease and microorganisms was evaluated. The presence ofCandida albicans-specific IgM and IgG antibodies in serum samples and the presence ofC. albicans in stool and c...
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Article
Formation of nanoporous platinum by selective dissolution of Cu from Cu0.75Pt0.25
This paper gives results demonstrating the production of nanoporous platinum through the de-alloying of Cu0.75Pt0.25 alloy in 1 M H2SO4. Both field emission scanning electron microscopy and small angle neutron sc...
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Article
Maple syrup urine disease: Mutation analysis in Turkish patients
Maple syrup urine disease (MSUD), the most frequently occurring organic acidaemia in Turkey, is caused by a deficiency of the activity of branched-chain keto acid dehydrogenase enzyme (BCKAD) complex. Mutation...
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Article
Mutation analysis in Turkish patients with hereditary fructose intolerance
Thirteen Turkish patients with hereditary fructose intolerance (HFI) were screened for the three common mutations, A149P, A174D and N334K, in the aldolase B gene that have been detected frequently in European ...
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Article
Neuroleptic malignant syndrome in a patient with citrullinaemia
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Effect of micro-element application on mineral composition and yield of spinach (spinacia oleracea) grown in soils with different lime contents
This study was undertaken to determine the effects of soil or foliage applied microplex fertilizer (5.4 %Mg, 4% Mn, 4% Fe, 1.5 % Cu, 1.5 % Zn, 0.5 % B, 0.1 % Mo and 0.05 % Co) on dry matter and mineral content...
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Macro and micro nutrient contents of tomato (Lycopersicon esculentum) and eggplant (Solatium melongena var. Esculentum) seedlings and their effects on seedling growth in relation to humic acid application
Plant performance mainly depends on characteristics of photosynthetically active organs. Many of these characteristics such as growth performance and quality of seedlings are modified by ecological conditions ...
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Article
Incisional healing in rats treated with diethyl maleate
Diethyl maleate (DEM) which binds and thus depletes tissue glutathione levels was used to aggravate the injury and to determine its effect on incisional healing. A 5 cm dorsal midline skin incision was perform...
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Article
Neutral lipid storage disease co-existing with ichthyosiform dermatosis