Search Results - "Cansever, M. Şerif"
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Separation and quantification of the urinary enantiomers of 2‐hydroxyglutaric acid by capillary electrophoresis with capacitively coupled contactless conductivity detection: Application to the diagnosis of D‐ and L‐2‐hydroxyglutaric aciduria
Published in Journal of separation science (01-08-2023)“…2‐hydroxyglutaric aciduria is an inherited neurometabolic disorder with two major types: D‐2‐hydroxyglutaric aciduria and L‐2‐hydroxyglutaric aciduria. An easy…”
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Analysis of Biotinidase Activity in Serum by Digital Imaging Colorimetry Detection
Published in ACS omega (24-10-2023)“…Biotinidase deficiency (BD) is an autosomal recessive inherited disorder of biotin recycling that leads to neurological and cutaneous consequences if left…”
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Determination of homogentisic acid in urine for diagnosis of alcaptonuria: Capillary electrophoretic method optimization using experimental design
Published in Biomedical chromatography (01-07-2018)“…Homogentisic acid (HGA) is a diagnostic metabolite that accumulates in the urine and tissues of patients with alkaptonuria which is a rare autosomal recessive…”
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Carbonyl ylide reactions of α-benzylidene-β-dicarbonyl compounds: competitive formation of dihydrofurans and dihydrobenzoxepines
Published in Tetrahedron letters (04-02-2008)“…α-Benzylidene-β,β′-biscarbonyl compounds were reacted with dimethyl diazomalonate using Cu(II) acetylacetonate as a catalyst. Dihydrofurans or mixtures of…”
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Determination of NTBC in serum samples from patients with hereditary tyrosinemia type I by capillary electrophoresis
Published in Talanta (Oxford) (15-03-2010)“…Hereditary tyrosinemia type I is a serious metabolic disorder leading to liver failure. 2-(2-Nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC) is a…”
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Hereditary Tyrosinemia Type 1 in Turkey
Published in Advances in experimental medicine and biology (2017)“…Hereditary tyrosinemia type 1 (HT1, OMIM 276700) is a rare autosomal recessively inherited inborn error of metabolism in the tyrosine catabolic pathway due to…”
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Determination of urinary succinylacetone by capillary electrophoresis for the diagnosis of tyrosinemia type I
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (25-04-2005)“…The presence of succinylacetone in urine or blood or amniotic fluid is pathognomonic of an inherited metabolic disorder, named tyrosinemia type I. We developed…”
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Reactions of α , β ‐Enones with Diazo Compounds. Part 4: Reaction Pathways from ( Z )‐ and ( E )‐ α , β ‐Enones with Dimethyl Diazomalonate
Published in Helvetica chimica acta (01-01-2004)“…Abstract In this study, ( E )‐ and ( Z )‐enones carrying only a phenyl substituent at their C( β ) atom were treaced with dimethyl diazomalonate in the…”
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Interscalene Brachial Plexus Block with Bupivacaine and Ropivacaine in Patients with Chronic Renal Failure: Diaphragmatic Excursion and Pulmonary Function Changes
Published in Anesthesia and analgesia (01-04-2005)“…In this randomized, double-blind study, we compared the anesthetic characteristics and pulmonary function changes of 0.33% bupivacaine and 0.33% ropivacaine…”
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Reactions of α,β-Enones with Diazo Compounds. Part 4
Published in Helvetica chimica acta (01-02-2004)“…In this study, (E)‐ and (Z)‐enones carrying only a phenyl substituent at their C(β) atom were treaced with dimethyl diazomalonate in the presence of…”
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Bir olgu nedeniyle piridoksin bağımlı nöbetler
Published in Medical journal of Bakirköy (2010)“…Piridoksin bağımlılığı yenidoğan ve süt çocukluğu döneminde nadir ortaya çıkabilen konvülsiyon nedenlerindendir. Piridoksin bağımlı nöbetler antikonvülzanlara…”
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