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Journal Abstract Search

254 related items for PubMed ID: 24696406

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  • 5. Monoamine neurotransmitter disorders--clinical advances and future perspectives.
    Ng J, Papandreou A, Heales SJ, Kurian MA.
    Nat Rev Neurol; 2015 Oct; 11(10):567-84. PubMed ID: 26392380
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  • 6. [Pediatric neurotransmitter disease in Japan].
    Shintaku H.
    No To Hattatsu; 2012 Sep; 44(5):361-7. PubMed ID: 23012864
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  • 8. Movement Disorders in Treatable Inborn Errors of Metabolism.
    Ebrahimi-Fakhari D, Van Karnebeek C, Münchau A.
    Mov Disord; 2019 May; 34(5):598-613. PubMed ID: 30557456
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  • 10. Neuroimaging Spectrum of Inherited Neurotransmitter Disorders.
    Lim YT, Mankad K, Kinali M, Tan AP.
    Neuropediatrics; 2020 Feb; 51(1):6-21. PubMed ID: 31634934
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  • 12. A case report of infantile parkinsonism-dystonia-2 caused by homozygous mutation in the SLC18A2 gene.
    Zhai H, Zheng Y, He Y, Zhang Y, Guo Z, Cui W, Sun L.
    Int J Neurosci; 2023 May; 133(5):574-577. PubMed ID: 34078222
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  • 14. Presentation, diagnosis, and treatment of the disorders of monoamine neurotransmitter metabolism.
    Hyland K.
    Semin Perinatol; 1999 Apr; 23(2):194-203. PubMed ID: 10331470
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  • 15. Neuroimaging findings in children with paediatric neurotransmitter diseases.
    Lee WT, Weng WC, Peng SF, Tzen KY.
    J Inherit Metab Dis; 2009 Jun; 32(3):361-70. PubMed ID: 19455403
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  • 18. Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesis.
    Hyland K, Surtees RA, Rodeck C, Clayton PT.
    Neurology; 1992 Oct; 42(10):1980-8. PubMed ID: 1357595
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