Search Results - "Cansever, M. Şerif"

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    Analysis of Biotinidase Activity in Serum by Digital Imaging Colorimetry Detection by Destanoğlu, Orhan, Cansever, M. Şerif, İşat, Esra, Zübarioğlu, Tanyel, Aktuğlu Zeybek, A. Çiğdem, Kıykım, Ertuğrul

    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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    Journal Article
  3. 3

    Determination of homogentisic acid in urine for diagnosis of alcaptonuria: Capillary electrophoretic method optimization using experimental design by Öztekin, Nevin, Balta, Gülfem S., Cansever, M. Şerif

    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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  4. 4

    Carbonyl ylide reactions of α-benzylidene-β-dicarbonyl compounds: competitive formation of dihydrofurans and dihydrobenzoxepines by Anaç, Olcay, Sezer, Özkan, Candan, Özlem, Güngör, Füsun Şeyma, Cansever, M. Şerif

    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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    Journal Article
  5. 5

    Determination of NTBC in serum samples from patients with hereditary tyrosinemia type I by capillary electrophoresis by Cansever, M. Şerif, Aktuğlu-Zeybek, A. Çiğdem, Erim, F. Bedia

    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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  6. 6

    Hereditary Tyrosinemia Type 1 in Turkey by Aktuglu-Zeybek, Ayse Cigdem, Kiykim, Ertugrul, Cansever, M Serif

    “…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 by Cansever, M Serif, Erim, F Bedia

    “…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 by Anaç, Olcay, Güngör, Füsun Seyma, Kahveci, Çiĝdem, Cansever, M. Şerif

    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 by Altintas, Fatis, Gumus, Funda, Kaya, Guner, Mihmanli, Ismail, Kantarci, Fatih, Kaynak, Kamil, Cansever, M Serif

    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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  10. 10

    Reactions of α,β-Enones with Diazo Compounds. Part 4 by Anaç, Olcay, Güngör, Füsun Seyma, Kahveci, Çiĝdem, Cansever, M. Şerif

    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 by TOPAL, Nilüfer, CANSEVER, M. Şerif, ÜNVER, Olcay, AYDIN, Ahmet, SOYUÇEN, Erdoğan

    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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