These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 12438171)

  • 1. Genetic basis of clinical catecholamine disorders.
    Garland EM; Hahn MK; Ketch TP; Keller NR; Kim CH; Kim KS; Biaggioni I; Shannon JR; Blakely RD; Robertson D
    Ann N Y Acad Sci; 2002 Oct; 971():506-14. PubMed ID: 12438171
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The broader view: catecholamine abnormalities.
    Vincent S; Robertson D
    Clin Auton Res; 2002 May; 12 Suppl 1():I44-9. PubMed ID: 12102462
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial orthostatic tachycardia due to norepinephrine transporter deficiency.
    Robertson D; Flattem N; Tellioglu T; Carson R; Garland E; Shannon JR; Jordan J; Jacob G; Blakely RD; Biaggioni I
    Ann N Y Acad Sci; 2001 Jun; 940():527-43. PubMed ID: 11458707
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Orthostatic intolerance and tachycardia associated with norepinephrine-transporter deficiency.
    Shannon JR; Flattem NL; Jordan J; Jacob G; Black BK; Biaggioni I; Blakely RD; Robertson D
    N Engl J Med; 2000 Feb; 342(8):541-9. PubMed ID: 10684912
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 148(36):1771-5. PubMed ID: 15495941
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 108(2):140-7. PubMed ID: 11857564
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 1(3 Pt 1):231-8. PubMed ID: 3291893
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hyperinsulinemia and Insulin Resistance in Dopamine β-Hydroxylase Deficiency.
    Arnold AC; Garland EM; Celedonio JE; Raj SR; Abumrad NN; Biaggioni I; Robertson D; Luther JM; Shibao CA
    J Clin Endocrinol Metab; 2017 Jan; 102(1):10-14. PubMed ID: 27778639
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical presentation and long-term follow-up of dopamine beta hydroxylase deficiency.
    Wassenberg T; Deinum J; van Ittersum FJ; Kamsteeg EJ; Pennings M; Verbeek MM; Wevers RA; van Albada ME; Kema IP; Versmissen J; van den Meiracker T; Lenders JWM; Monnens L; Willemsen MA
    J Inherit Metab Dis; 2021 May; 44(3):554-565. PubMed ID: 33034372
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Regulation of norepinephrine transporter abundance by catecholamines and desipramine in vivo.
    Weinshenker D; White SS; Javors MA; Palmiter RD; Szot P
    Brain Res; 2002 Aug; 946(2):239-46. PubMed ID: 12137927
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dopamine beta-hydroxylase deficiency. A genetic disorder of cardiovascular regulation.
    Robertson D; Haile V; Perry SE; Robertson RM; Phillips JA; Biaggioni I
    Hypertension; 1991 Jul; 18(1):1-8. PubMed ID: 1677640
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital dopamine-beta-hydroxylase deficiency. A novel orthostatic syndrome.
    Man in 't Veld AJ; Boomsma F; Moleman P; Schalekamp MA
    Lancet; 1987 Jan; 1(8526):183-8. PubMed ID: 2880016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in
    van den Berg MP; Almomani R; Biaggioni I; van Faassen M; van der Harst P; Silljé HHW; Mateo Leach I; Hemmelder MH; Navis G; Luijckx GJ; de Brouwer APM; Venselaar H; Verbeek MM; van der Zwaag PA; Jongbloed JDH; van Tintelen JP; Wevers RA; Kema IP
    Circ Res; 2018 Mar; 122(6):846-854. PubMed ID: 29343526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Norepinephrine deficiency is caused by combined abnormal mRNA processing and defective protein trafficking of dopamine beta-hydroxylase.
    Kim CH; Leung A; Huh YH; Yang E; Kim DJ; Leblanc P; Ryu H; Kim K; Kim DW; Garland EM; Raj SR; Biaggioni I; Robertson D; Kim KS
    J Biol Chem; 2011 Mar; 286(11):9196-204. PubMed ID: 21209083
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Orthostatic intolerance is not necessarily related to a specific mutation (Ala457Pro) in the human norepinephrine transporter gene.
    Ivancsits S; Heider A; Rüdiger HW; Winker R
    Am J Med Sci; 2003 Feb; 325(2):63-5. PubMed ID: 12589229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout Mice.
    Cubells JF; Schroeder JP; Barrie ES; Manvich DF; Sadee W; Berg T; Mercer K; Stowe TA; Liles LC; Squires KE; Mezher A; Curtin P; Perdomo DL; Szot P; Weinshenker D
    PLoS One; 2016; 11(5):e0154864. PubMed ID: 27148966
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal cardiovascular and catecholamine responses to supine exercise in human subjects with sympathetic dysfunction.
    Smith GD; Watson LP; Pavitt DV; Mathias CJ
    J Physiol; 1995 Apr; 484 ( Pt 1)(Pt 1):255-65. PubMed ID: 7602525
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dopamine beta-hydroxylase deficiency.
    Senard JM; Rouet P
    Orphanet J Rare Dis; 2006 Mar; 1():7. PubMed ID: 16722595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effects of dopamine beta-hydroxylase genotype and disulfiram inhibition on catecholamine homeostasis in mice.
    Bourdélat-Parks BN; Anderson GM; Donaldson ZR; Weiss JM; Bonsall RW; Emery MS; Liles LC; Weinshenker D
    Psychopharmacology (Berl); 2005 Nov; 183(1):72-80. PubMed ID: 16163519
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DBH gene variants that cause low plasma dopamine beta hydroxylase with or without a severe orthostatic syndrome.
    Deinum J; Steenbergen-Spanjers GC; Jansen M; Boomsma F; Lenders JW; van Ittersum FJ; Hück N; van den Heuvel LP; Wevers RA
    J Med Genet; 2004 Apr; 41(4):e38. PubMed ID: 15060114
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.