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Journal Abstract Search

371 related items for PubMed ID: 30587156

  • 1. Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report.
    Hong D, Yu Y, Wang Y, Xu Y, Zhang J.
    BMC Neurol; 2018 Dec 26; 18(1):219. PubMed ID: 30587156
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  • 6. Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report.
    Goh LL, Lee Y, Tan ES, Lim JSC, Lim CW, Dalan R.
    BMC Med Genomics; 2018 Apr 03; 11(1):37. PubMed ID: 29615056
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  • 7. Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency.
    Yıldız Y, Talim B, Haliloglu G, Topaloglu H, Akçören Z, Dursun A, Sivri HS, Coşkun T, Tokatlı A.
    Pediatr Neurol; 2019 Oct 03; 99():69-75. PubMed ID: 31331668
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  • 8. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Law LK, Tang NL, Hui J, Fung SL, Ruiter J, Wanders RJ, Fok TF, Lam CW.
    Clin Chim Acta; 2009 Jun 27; 404(2):95-9. PubMed ID: 19265687
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  • 12. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease.
    Béhin A, Acquaviva-Bourdain C, Souvannanorath S, Streichenberger N, Attarian S, Bassez G, Brivet M, Fouilhoux A, Labarre-Villa A, Laquerrière A, Pérard L, Kaminsky P, Pouget J, Rigal O, Vanhulle C, Eymard B, Vianey-Saban C, Laforêt P.
    Rev Neurol (Paris); 2016 Mar 27; 172(3):231-41. PubMed ID: 27038534
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  • 14. Investigation of adult-onset multiple acyl-CoA dehydrogenase deficiency associated with peripheral neuropathy.
    Huang K, Duan HQ, Li QX, Luo YB, Yang H.
    Neuropathology; 2020 Dec 27; 40(6):531-539. PubMed ID: 32608139
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  • 18. Molecular and Clinical Investigations on Portuguese Patients with Multiple acyl-CoA Dehydrogenase Deficiency.
    Henriques BJ, Lucas TG, Martins E, Gaspar A, Bandeira A, Nogueira C, Brandão O, Rocha H, Vilarinho L, Gomes CM.
    Curr Mol Med; 2019 Dec 27; 19(7):487-493. PubMed ID: 31418342
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