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Journal Abstract Search

163 related items for PubMed ID: 9645154

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

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

  • 3. Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines.
    Lamers KJ, Wevers RA.
    Mult Scler; 1998 Feb; 4(1):37-8. PubMed ID: 9532591
    [Abstract] [Full Text] [Related]

  • 4. Genetics and molecular biology of hypotension.
    Robertson D.
    Curr Opin Nephrol Hypertens; 1994 Jan; 3(1):13-24. PubMed ID: 7850407
    [Abstract] [Full Text] [Related]

  • 5. Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies.
    Fiumara A, Bräutigam C, Hyland K, Sharma R, Lagae L, Stoltenborg B, Hoffmann GF, Jaeken J, Wevers RA.
    Neuropediatrics; 2002 Aug; 33(4):203-8. PubMed ID: 12368991
    [Abstract] [Full Text] [Related]

  • 6. Monoamine neurotransmitter deficiencies.
    Pearl PL.
    Handb Clin Neurol; 2013 Aug; 113():1819-25. PubMed ID: 23622404
    [Abstract] [Full Text] [Related]

  • 7. [A deficiency of dihydrobiopterin synthesis. The effects of L-dopa, 5HTP and BH4].
    Fujita N, Tanaka K, Nakajima T, Miyatake T, Ohwada M.
    Rinsho Shinkeigaku; 1988 Apr; 28(4):376-81. PubMed ID: 3265083
    [No Abstract] [Full Text] [Related]

  • 8. Catecholamine phenotyping: clues to the diagnosis, treatment, and pathophysiology of neurogenetic disorders.
    Goldstein DS, Lenders JW, Kaler SG, Eisenhofer G.
    J Neurochem; 1996 Nov; 67(5):1781-90. PubMed ID: 8863481
    [Abstract] [Full Text] [Related]

  • 9. [Disorders of tetrahydrobiopterin homeostasis].
    Shintaku H, Asada M, Isshiki G, Sawada Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Nov; (18 Pt 1):125-9. PubMed ID: 9590005
    [No Abstract] [Full Text] [Related]

  • 10. Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family.
    Maller A, Hyland K, Milstien S, Biaggioni I, Butler IJ.
    J Child Neurol; 1997 Sep; 12(6):349-54. PubMed ID: 9309516
    [Abstract] [Full Text] [Related]

  • 11. Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiency.
    Anselm IA, Darras BT.
    Pediatr Neurol; 2006 Aug; 35(2):142-4. PubMed ID: 16876014
    [Abstract] [Full Text] [Related]

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

  • 13. DBH deficiency in an elderly patient: efficacy and safety of chronic droxidopa.
    Despas F, Pathak A, Berry M, Cagnac R, Massabuau P, Liozon E, Galinier M, Senard JM.
    Clin Auton Res; 2010 Jun; 20(3):205-7. PubMed ID: 20063034
    [Abstract] [Full Text] [Related]

  • 14. Stress-induced alterations in catecholamine enzymes gene expression in the hypothalamic dorsomedial nucleus are modulated by caudal brain and not hypothalamic paraventricular nucleus neurons.
    Mravec B, Lukackova R, Bodnar I, Kiss A, Pacak K, Palkovits M, Kvetnansky R.
    Brain Res Bull; 2007 Sep 14; 74(1-3):147-54. PubMed ID: 17683801
    [Abstract] [Full Text] [Related]

  • 15. [Mevalonic aciduria].
    Yoshida I.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 14; (18 Pt 1):305-9. PubMed ID: 9590053
    [No Abstract] [Full Text] [Related]

  • 16. [N5-methyltetrahydrofolate: homocysteine methyltransferase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 14; (18 Pt 1):267-8. PubMed ID: 9590043
    [No Abstract] [Full Text] [Related]

  • 17. Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency.
    Bräutigam C, Hyland K, Wevers R, Sharma R, Wagner L, Stock GJ, Heitmann F, Hoffmann GF.
    Neuropediatrics; 2002 Jun 14; 33(3):113-7. PubMed ID: 12200739
    [Abstract] [Full Text] [Related]

  • 18. [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 14; 20(3):195-9. PubMed ID: 3260512
    [No Abstract] [Full Text] [Related]

  • 19. [Lipoamide dehydrogenase deficiency].
    Ito M, Matsuda J.
    Ryoikibetsu Shokogun Shirizu; 1998 May 14; (18 Pt 1):341-2. PubMed ID: 9590063
    [No Abstract] [Full Text] [Related]

  • 20. Aromatic L-amino acid decarboxylase deficiency associated with epilepsy mimicking non-epileptic involuntary movements.
    Ito S, Nakayama T, Ide S, Ito Y, Oguni H, Goto Y, Osawa M.
    Dev Med Child Neurol; 2008 Nov 14; 50(11):876-8. PubMed ID: 18754761
    [Abstract] [Full Text] [Related]

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