Works matching AU Ozlu, Can


Results: 21
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    Developmental phenotype and quality of life in SLC13A5 citrate transporter disorder.

    Published in:
    Developmental Medicine & Child Neurology, 2025, v. 67, n. 7, p. 930, doi. 10.1111/dmcn.16218
    By:
    • Ozlu, Can;
    • Adams, Raegan M.;
    • Solidum, Rayann M.;
    • Cooper, Sydney;
    • Best, Carrie R.;
    • Elacio, Jennifer;
    • Kavanaugh, Brian C.;
    • Spelbrink, Emily M.;
    • Brown, Tanya L.;
    • Nye, Kimberly;
    • Liu, Judy S.;
    • Bailey, Rachel M.;
    • Goodspeed, Kimberly;
    • Porter, Brenda E.
    Publication type:
    Article
    3

    Sleep Abnormalities in SLC13A5 Citrate Transporter Disorder.

    Published in:
    Genes, 2024, v. 15, n. 10, p. 1338, doi. 10.3390/genes15101338
    By:
    • Adams, Raegan M.;
    • Ozlu, Can;
    • Bailey, Lauren E.;
    • Solidum, Rayann M.;
    • Cooper, Sydney;
    • Best, Carrie R.;
    • Elacio, Jennifer;
    • Kavanaugh, Brian C.;
    • Brown, Tanya L.;
    • Nye, Kimberly;
    • Liu, Judy;
    • Porter, Brenda E.;
    • Goodspeed, Kimberly;
    • Bailey, Rachel M.
    Publication type:
    Article
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    ECHS1 deficiency and its biochemical and clinical phenotype.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2908, doi. 10.1002/ajmg.a.62895
    By:
    • Ozlu, Can;
    • Chelliah, Priya;
    • Dahshi, Hamza;
    • Horton, Daniel;
    • Edgar, Veronica B.;
    • Messahel, Souad;
    • Kayani, Saima
    Publication type:
    Article
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    Visfatin Levels in Subclinical Hypothyroidism.

    Published in:
    International Journal of Peptide Research & Therapeutics, 2016, v. 22, n. 1, p. 11, doi. 10.1007/s10989-015-9479-3
    By:
    • Fidan Yaylali, Guzin;
    • Turgut, Sebahat;
    • Akin, Fulya;
    • Ozkan, Seyma;
    • Tural, Mehmet;
    • Tunc Ata, Melek;
    • Ozlu, Can;
    • İsler, Kamil
    Publication type:
    Article