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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

217 related items for PubMed ID: 10437291

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  • 4. Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.
    Giovanniello T, Leuzzi V, Carducci C, Carducci C, Sabato ML, Artiola C, Santagata S, Pozzessere S, Antonozzi I.
    Neuropediatrics; 2007 Aug; 38(4):213-5. PubMed ID: 18058633
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  • 5. [Dopa-responsive dystonia (Segawa syndrome) with secondary skeleton deformity].
    Budrewicz SP, Góral M, Koszewicz M, Tarantowicz P, Podemski R.
    Wiad Lek; 2006 Aug; 59(9-10):713-5. PubMed ID: 17338136
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  • 6. [Autosomal-dominant DOPA-responsive dystonia, caused by mutations in the GTP-cyclohydrolase I gene].
    Nagatsu T, Ichinose H.
    Vopr Med Khim; 1998 Aug; 44(3):225-8. PubMed ID: 9703621
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  • 8. Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia.
    Hoffmann GF, Assmann B, Bräutigam C, Dionisi-Vici C, Häussler M, de Klerk JB, Naumann M, Steenbergen-Spanjers GC, Strassburg HM, Wevers RA.
    Ann Neurol; 2003 Aug; 54 Suppl 6():S56-65. PubMed ID: 12891655
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  • 9. Dopa-responsive dystonia -- the story so far.
    Bandmann O, Wood NW.
    Neuropediatrics; 2002 Feb; 33(1):1-5. PubMed ID: 11930268
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  • 10. Segawa's disease: dopa-responsive dystonia.
    Gordon N.
    Int J Clin Pract; 2008 Jun; 62(6):943-6. PubMed ID: 17971156
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  • 11. A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: clinical, biochemical and genetic analysis.
    Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal A, García-Cazorla A, Pérez-Dueñas B, Campistol J, Artuch R, Cormand B.
    Mol Genet Metab; 2007 Nov; 92(3):274-7. PubMed ID: 17698383
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  • 13. Dopa-responsive dystonia and Tourette syndrome in a large Danish family.
    Romstad A, Dupont E, Krag-Olsen B, Østergaard K, Guldberg P, Güttler F.
    Arch Neurol; 2003 Apr; 60(4):618-22. PubMed ID: 12707079
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  • 15. [Characteristics of the clinical course, pathogenesis and treatment of torsion dystonia in childhood].
    Markova ED.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989 Apr; 89(8):32-5. PubMed ID: 2588895
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  • 18. Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene.
    Verbeek MM, Steenbergen-Spanjers GC, Willemsen MA, Hol FA, Smeitink J, Seeger J, Grattan-Smith P, Ryan MM, Hoffmann GF, Donati MA, Blau N, Wevers RA.
    Ann Neurol; 2007 Oct; 62(4):422-6. PubMed ID: 17696123
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