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380 results

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Page 1
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. Robertson D, et al. Among authors: garland e. Ann N Y Acad Sci. 2001 Jun;940:527-43. doi: 10.1111/j.1749-6632.2001.tb03703.x. Ann N Y Acad Sci. 2001. PMID: 11458707 Review.
Multiple system atrophy: new developments in pathophysiology and therapy.
Robertson D, Shannon JR, Jordan J, Davis TL, Diedrich A, Jacob G, Garland E, Tellioglu T, Biaggioni I. Robertson D, et al. Among authors: garland e. Parkinsonism Relat Disord. 2001 Jul;7(3):257-260. doi: 10.1016/s1353-8020(00)00067-5. Parkinsonism Relat Disord. 2001. PMID: 11331196
Genetic polymorphisms of adrenergic receptors.
Garland EM, Biaggioni I. Garland EM, et al. Clin Auton Res. 2001 Apr;11(2):67-78. doi: 10.1007/BF02322049. Clin Auton Res. 2001. PMID: 11570606 Review.
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. Garland EM, et al. Ann N Y Acad Sci. 2002 Oct;971:506-14. doi: 10.1111/j.1749-6632.2002.tb04515.x. Ann N Y Acad Sci. 2002. PMID: 12438171 Review.
Fragile X gene premutation in multiple system atrophy.
Garland EM, Vnencak-Jones CL, Biaggioni I, Davis TL, Montine TJ, Robertson D. Garland EM, et al. J Neurol Sci. 2004 Dec 15;227(1):115-8. doi: 10.1016/j.jns.2004.08.013. J Neurol Sci. 2004. PMID: 15546601
Endothelial NO synthase polymorphisms and postural tachycardia syndrome.
Garland EM, Winker R, Williams SM, Jiang L, Stanton K, Byrne DW, Biaggioni I, Cascorbi I, Phillips JA 3rd, Harris PA, Rüdiger H, Robertson D. Garland EM, et al. Hypertension. 2005 Nov;46(5):1103-10. doi: 10.1161/01.HYP.0000185462.08685.da. Epub 2005 Oct 3. Hypertension. 2005. PMID: 16203873
380 results