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Journal Abstract Search

63 related items for PubMed ID: 11462573

  • 1. [Dopamin beta-hydroxylase deficiency, congenital].
    Yokoyama Y.
    Ryoikibetsu Shokogun Shirizu; 2001; (33):567-8. PubMed ID: 11462573
    [No Abstract] [Full Text] [Related]

  • 2. Congenital dopamine-beta-hydroxylase deficiency in humans.
    Timmers HJ, Deinum J, Wevers RA, Lenders JW.
    Ann N Y Acad Sci; 2004 Jun; 1018():520-3. PubMed ID: 15240410
    [Abstract] [Full Text] [Related]

  • 3. [Inborn errors of catecholamine metabolism].
    Suzuki T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jun; (19 Pt 2):640-4. PubMed ID: 9645154
    [No Abstract] [Full Text] [Related]

  • 4. Genetic diseases of hypotension.
    Robertson D, Hale N.
    Adv Pharmacol; 1998 Jun; 42():61-5. PubMed ID: 9327847
    [No Abstract] [Full Text] [Related]

  • 5. Dopamine in dopamine-beta-hydroxylase deficiency.
    Biaggioni I, Hollister AS, Robertson D.
    N Engl J Med; 1987 Nov 26; 317(22):1415-6. PubMed ID: 3683474
    [No Abstract] [Full Text] [Related]

  • 6. [Inborn errors of catecholamine metabolism].
    Suzuki T.
    Ryoikibetsu Shokogun Shirizu; 2000 Nov 26; (29 Pt 4):527-31. PubMed ID: 11032013
    [No Abstract] [Full Text] [Related]

  • 7. Dopamine beta-hydroxylase deficiency involves the central autonomic network.
    Cheshire WP, Dickson DW, Nahm KF, Kaufmann HC, Benarroch EE.
    Acta Neuropathol; 2006 Aug 26; 112(2):227-9. PubMed ID: 16830134
    [No Abstract] [Full Text] [Related]

  • 8. [From gene to disease; dopamine-beta-hydroxylase deficiency and orthostatic hypotension].
    Deinum J, van den Meiracker AH, Boomsma F, van Ittersum FJ, Wevers RA, Lenders JW.
    Ned Tijdschr Geneeskd; 2004 Sep 04; 148(36):1771-5. PubMed ID: 15495941
    [Abstract] [Full Text] [Related]

  • 9. [Combined use of tandem mass spectrometry with urine gas chromatography/mass spectrometry is useful for diagnosis of inborn errors of metabolism in children].
    Xie LJ, Zhu JX, Zhu XD, Li HJ, Han LS, Gu XF.
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb 04; 10(1):31-4. PubMed ID: 18289467
    [Abstract] [Full Text] [Related]

  • 10. The failure to diagnose inborn errors of metabolism in New Zealand: the case for expanded newborn screening.
    Wilson C, Kerruish NJ, Wilcken B, Wiltshire E, Webster D.
    N Z Med J; 2007 Sep 21; 120(1262):U2727. PubMed ID: 17891215
    [Abstract] [Full Text] [Related]

  • 11. Acquired and inherited disorders of cobalamin and folate in children.
    Whitehead VM.
    Br J Haematol; 2006 Jul 21; 134(2):125-36. PubMed ID: 16846473
    [Abstract] [Full Text] [Related]

  • 12.
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    [No Abstract] [Full Text] [Related]

  • 13. [Three congenital metabolic diseases in the Faeroe Islands. Incidence, clinical and molecular genetic characteristics of Faeroese children with glycogen storage disease type IIIA, carnitine transporter deficiency and holocarboxylase synthetase deficiency].
    Joensen F, Steuerwald EU, Rasmussen NH.
    Ugeskr Laeger; 2006 Feb 13; 168(7):667-70. PubMed ID: 16494802
    [Abstract] [Full Text] [Related]

  • 14. Inborn errors of metabolism in infancy and early childhood: an update.
    Raghuveer TS, Garg U, Graf WD.
    Am Fam Physician; 2006 Jun 01; 73(11):1981-90. PubMed ID: 16770930
    [Abstract] [Full Text] [Related]

  • 15. [Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience].
    Cerone R, Cassanello M, Caruso U, Schiaffino MC, Lorini R.
    Minerva Pediatr; 2007 Oct 01; 59(5):488-9. PubMed ID: 17947884
    [No Abstract] [Full Text] [Related]

  • 16. Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency.
    Kim CH, Zabetian CP, Cubells JF, Cho S, Biaggioni I, Cohen BM, Robertson D, Kim KS.
    Am J Med Genet; 2002 Mar 01; 108(2):140-7. PubMed ID: 11857564
    [Abstract] [Full Text] [Related]

  • 17. [Inborn errors of metabolism with neurological manifestations in the neonatal period].
    Campistol J.
    Medicina (B Aires); 2007 Mar 01; 67(6 Pt 1):561-8. PubMed ID: 18422082
    [Abstract] [Full Text] [Related]

  • 18. [Inborn errors of metabolism with neurological symptomathology in the neonatal period].
    Campistol J, Málaga-Diéguez I, García-Cazorla A, Krauel-Vidal X, Vilaseca MA.
    Rev Neurol; 2007 Mar 01; 40(6):321-6. PubMed ID: 15795866
    [Abstract] [Full Text] [Related]

  • 19. Newborn screening in the Philippines.
    Padilla CD.
    Southeast Asian J Trop Med Public Health; 2003 Mar 01; 34 Suppl 3():87-8. PubMed ID: 15906705
    [Abstract] [Full Text] [Related]

  • 20. Biochemical findings in common inborn errors of metabolism.
    Pasquali M, Monsen G, Richardson L, Alston M, Longo N.
    Am J Med Genet C Semin Med Genet; 2006 May 15; 142C(2):64-76. PubMed ID: 16602099
    [Abstract] [Full Text] [Related]

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