Works matching Fatty acid oxidation disorders


Results: 358
    1
    2
    3
    5

    Living on the edge: substrate competition explains loss of robustness in mitochondrial fatty-acid oxidation disorders.

    Published in:
    BMC Biology, 2016, v. 14, p. 1, doi. 10.1186/s12915-016-0327-5
    By:
    • van Eunen, Karen;
    • Volker-Touw, Catharina M. L.;
    • Gerding, Albert;
    • Bleeker, Aycha;
    • Wolters, Justina C.;
    • van Rijt, Willemijn J.;
    • Martines, Anne-Claire M. F.;
    • Niezen-Koning, Klary E.;
    • Heiner, Rebecca M.;
    • Permentier, Hjalmar;
    • Groen, Albert K.;
    • Reijngoud, Dirk-Jan;
    • Derks, Terry G. J.;
    • Bakker, Barbara M.
    Publication type:
    Article
    6

    Sudden Death of a Four-Day-Old Newborn Due to Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiencies and a Systematic Literature Review of Early Deaths of Neonates with Fatty Acid Oxidation Disorders.

    Published in:
    International Journal of Neonatal Screening (IJNS), 2025, v. 11, n. 1, p. 9, doi. 10.3390/ijns11010009
    By:
    • Drole Torkar, Ana;
    • Klinc, Ana;
    • Remec, Ziga Iztok;
    • Rankovic, Branislava;
    • Bartolj, Klara;
    • Bertok, Sara;
    • Colja, Sara;
    • Cuk, Vanja;
    • Debeljak, Marusa;
    • Kozjek, Eva;
    • Repic Lampret, Barbka;
    • Mlinaric, Matej;
    • Mohar Hajnsek, Tinka;
    • Perko, Daša;
    • Stajer, Katarina;
    • Tesovnik, Tine;
    • Trampuz, Domen;
    • Ulaga, Blanka;
    • Kovac, Jernej;
    • Battelino, Tadej
    Publication type:
    Article
    7

    Sepsis Tablosunda Gelen Yağ Asidi Oksidasyon Bozukluğu.

    Published in:
    Journal of the Child / Çocuk Dergisi, 2014, v. 14, n. 3, p. 125, doi. 10.5222/j.child.2014.125
    By:
    • ALP, Emel EKŞİ;
    • CEBECİ, Sinem ORAL;
    • UYSALOL, Metin;
    • ÇITAK, Agop;
    • KARACA, Meryem;
    • ERTÜRK, Tuğçe
    Publication type:
    Article
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45

    Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders.

    Published in:
    Annals of Clinical & Translational Neurology, 2024, v. 11, n. 4, p. 883, doi. 10.1002/acn3.52002
    By:
    • Mütze, Ulrike;
    • Ottenberger, Alina;
    • Gleich, Florian;
    • Maier, Esther M.;
    • Lindner, Martin;
    • Husain, Ralf A.;
    • Palm, Katja;
    • Beblo, Skadi;
    • Freisinger, Peter;
    • Santer, René;
    • Thimm, Eva;
    • vom Dahl, Stephan;
    • Weinhold, Natalie;
    • Grohmann‐Held, Karina;
    • Haase, Claudia;
    • Hennermann, Julia B.;
    • Hörbe‐Blindt, Alexandra;
    • Kamrath, Clemens;
    • Marquardt, Iris;
    • Marquardt, Thorsten
    Publication type:
    Article
    46
    47
    48

    Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency.

    Published in:
    Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-102
    By:
    • Couce, Maria Luz;
    • Sánchez-Pintos, Paula;
    • Diogo, Luisa;
    • Leão-Teles, Elisa;
    • Martins, Esmeralda;
    • Santos, Helena;
    • Bueno, Maria Amor;
    • Delgado-Pecellín, Carmen;
    • Castiñeiras, Daisy E.;
    • Cocho, José A.;
    • García-Villoria, Judit;
    • Ribes, Antonia;
    • Fraga, José M.;
    • Rocha, Hugo
    Publication type:
    Article
    49
    50