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Journal Abstract Search

121 related items for PubMed ID: 8863481

  • 1. 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]

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

  • 3. Genetic basis of autonomic dysfunction.
    Taneja I, Robertson D.
    Semin Neurol; 2003 Dec; 23(4):391-7. PubMed ID: 15088260
    [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. Monoamine neurotransmitter deficiencies.
    Pearl PL.
    Handb Clin Neurol; 2013 Jan; 113():1819-25. PubMed ID: 23622404
    [Abstract] [Full Text] [Related]

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

  • 7. Practical approaches to neurogenetic disease.
    Lynch DR, Farmer J.
    J Neuroophthalmol; 2002 Dec; 22(4):297-304. PubMed ID: 12464734
    [Abstract] [Full Text] [Related]

  • 8. Neurogenetic diseases: molecular diagnosis and therapeutic approaches.
    Muller U, Graeber MB.
    J Mol Med (Berl); 1996 Feb; 74(2):71-84. PubMed ID: 8820402
    [Abstract] [Full Text] [Related]

  • 9. Plasma and cerebrospinal fluid neurochemical pattern in Menkes disease.
    Kaler SG, Goldstein DS, Holmes C, Salerno JA, Gahl WA.
    Ann Neurol; 1993 Feb; 33(2):171-5. PubMed ID: 8434878
    [Abstract] [Full Text] [Related]

  • 10. [Molecular diagnosis of pediatric neurogenetic disorders: the present status and future in China].
    Wu XR, Zhong N.
    Zhonghua Er Ke Za Zhi; 2006 Jul; 44(7):481-3. PubMed ID: 17044969
    [No Abstract] [Full Text] [Related]

  • 11. Introduction: Behavioral phenotypes in neurogenetic syndromes.
    Battaglia A, Fisch GS.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):387-8. PubMed ID: 20981767
    [No Abstract] [Full Text] [Related]

  • 12. A defect in catecholamine metabolism in kinky-hair disease.
    Grover WD, Henkin RI, Schwartz M, Brodsky N, Hobdell E, Stolk JM.
    Ann Neurol; 1982 Sep 15; 12(3):263-6. PubMed ID: 7137961
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines.
    Lamers KJ, Wevers RA.
    Mult Scler; 1998 Feb 14; 4(1):37-8. PubMed ID: 9532591
    [Abstract] [Full Text] [Related]

  • 15. Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.
    Lenders JW, Eisenhofer G, Abeling NG, Berger W, Murphy DL, Konings CH, Wagemakers LM, Kopin IJ, Karoum F, van Gennip AH, Brunner HG.
    J Clin Invest; 1996 Feb 15; 97(4):1010-9. PubMed ID: 8613523
    [Abstract] [Full Text] [Related]

  • 16. Psychiatric phenotypes associated with neurogenetic disorders.
    Feinstein C, Chahal L.
    Psychiatr Clin North Am; 2009 Mar 15; 32(1):15-37. PubMed ID: 19248914
    [Abstract] [Full Text] [Related]

  • 17. Catecholaminergic signalling through thymic nerve fibres, thymocytes and stromal cells is dependent on both circulating and locally synthesized glucocorticoids.
    Pilipović I, Radojević K, Perišić M, Kosec D, Nacka-Aleksić M, Djikić J, Leposavić G.
    Exp Physiol; 2012 Nov 15; 97(11):1211-23. PubMed ID: 22562811
    [Abstract] [Full Text] [Related]

  • 18. [The monoamines in molluscs. I. Catecholamines: biosynthesis, disposition and inactivation (author's transl)].
    Cardot J.
    J Physiol (Paris); 1979 Nov 15; 75(7):689-713. PubMed ID: 44729
    [Abstract] [Full Text] [Related]

  • 19. Patients with congenital dopamine beta-hydroxylase deficiency. A lesson in catecholamine physiology.
    Man in 't Veld A, Boomsma F, Lenders J, vd Meiracker A, Julien C, Tulen J, Moleman P, Thien T, Lamberts S, Schalekamp M.
    Am J Hypertens; 1988 Jul 15; 1(3 Pt 1):231-8. PubMed ID: 3291893
    [Abstract] [Full Text] [Related]

  • 20. Aromatic L-amino acid decarboxylase, dopamine beta-hydroxylase, monoamine oxidase, malondialdehyde, and acid phosphatase in rat brain capillaries and kidney glomeruli in experimental hypertension.
    Valli VV, Sadasivudu B.
    J Neurosci Res; 1985 Jul 15; 13(4):481-8. PubMed ID: 4009739
    [Abstract] [Full Text] [Related]

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