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Journal Abstract Search

126 related items for PubMed ID: 2477772

  • 1. Tetrahydrobiopterin administration in biopterin-deficient progressive dystonia with diurnal variation.
    Fink JK, Ravin P, Argoff CE, Levine RA, Brady RO, Hallett M, Barton NW.
    Neurology; 1989 Oct; 39(10):1393-5. PubMed ID: 2477772
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  • 2. Dystonia with marked diurnal variation associated with biopterin deficiency.
    Fink JK, Barton N, Cohen W, Lovenberg W, Burns RS, Hallett M.
    Neurology; 1988 May; 38(5):707-11. PubMed ID: 2452381
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  • 3. Effect of tetrahydrobiopterin and 5-hydroxytryptophan on hereditary progressive dystonia with marked diurnal fluctuation: a suggestion of the serotonergic system involvement.
    Ishida A, Takada G, Kobayashi Y, Toyoshima I, Takai K.
    Tohoku J Exp Med; 1988 Mar; 154(3):233-9. PubMed ID: 3259739
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  • 4. Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptoms.
    Tanaka K, Yoneda M, Nakajima T, Miyatake T, Owada M.
    Neurology; 1987 Mar; 37(3):519-22. PubMed ID: 2434882
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  • 5. Pterin abnormalities in dystonia: a metabolic marker with therapeutic implications.
    LeWitt PA, Miller LP, Levine RA, Lovenberg W, Newman RP, Papavasiliou A, Rayes A, Eldridge R, Burns RS.
    Adv Neurol; 1988 Mar; 50():193-201. PubMed ID: 2456675
    [No Abstract] [Full Text] [Related]

  • 6. Cerebrospinal fluid concentrations of pterins and metabolites of serotonin and dopamine in a pediatric reference population.
    Hyland K, Surtees RA, Heales SJ, Bowron A, Howells DW, Smith I.
    Pediatr Res; 1993 Jul; 34(1):10-4. PubMed ID: 7689195
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  • 7. Tetrahydrobiopterin and Parkinson's disease.
    Dissing IC, Güttler F, Pakkenberg H, Lou H, Gerdes AM, Lykkelund C, Rasmussen V.
    Acta Neurol Scand; 1989 Jun; 79(6):493-9. PubMed ID: 2476906
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  • 8. High-performance liquid chromatographic measurement of cerebrospinal fluid tetrahydrobiopterin, neopterin, homovanillic acid and 5-hydroxindoleacetic acid in neurological diseases.
    Candito M, Nagatsu T, Chambon P, Chatel M.
    J Chromatogr B Biomed Appl; 1994 Jul 01; 657(1):61-6. PubMed ID: 7524948
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  • 15. Sepiapterin reductase deficiency an autosomal recessive DOPA-responsive dystonia.
    Abeling NG, Duran M, Bakker HD, Stroomer L, Thöny B, Blau N, Booij J, Poll-The BT.
    Mol Genet Metab; 2006 Jul 01; 89(1-2):116-20. PubMed ID: 16650784
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  • 16. [Serotonergic disturbance in hereditary progressive dystonia--clinical effects of tetrahydrobiopterin and 5-hydroxytryptophan].
    Ishida A, Takada G, Kobayashi Y, Higashi O, Toyoshima I, Takai K.
    No To Hattatsu; 1988 May 01; 20(3):195-9. PubMed ID: 3260512
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  • 19. GTP-cyclohydrolase I gene mutations in hereditary progressive amd dopa-responsive dystonia.
    Furukawa Y, Shimadzu M, Rajput AH, Shimizu Y, Tagawa T, Mori H, Yokochi M, Narabayashi H, Hornykiewicz O, Mizuno Y, Kish SJ.
    Ann Neurol; 1996 May 01; 39(5):609-17. PubMed ID: 8619546
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  • 20. [Malignant phenylketonuria caused by biopterin synthetase deficiency. Study of neuromediator catabolites in the cerebrospinal fluid during treatment].
    Malpuech G, Guyon A, Demeocq F, Piton A, Boespflug O, Vanlieferinghen P.
    Arch Fr Pediatr; 1984 Jan 01; 41(1):5-8. PubMed ID: 6202269
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