PAPER Lo HS, Chen CH, Hogan EL, Kao KP, Wang V, Yan SH
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PAPER Liu QR, Walther D, Drgon T, Polesskaya O, Lesnick TG, Strain KJ, de Andrade M, Bower JH, Maraganore DM, Uhl GR
Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease.
Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):93-103. PubMed: 15666411PAPER Lincoln SJ, Maraganore DM, Lesnick TG, Bounds R, de Andrade M, Bower JH, Hardy JA, Farrer MJ
Parkin variants in North American Parkinson's disease: cases and controls.
Mov Disord. 2003 Nov;18(11):1306-11. PubMed: 14639672PAPER Lin JJ, Yueh KC, Chang CY, Chen CH, Lin SZ
The homozygote AA genotype of the alpha1-antichymotrypsin gene may confer protection against early-onset Parkinson's disease in women.
Parkinsonism Relat Disord. 2004 Dec;10(8):469-73. PubMed: 15542006PAPER Lee MS, Lyoo CH, Ulmanen I, Syvänen AC, Rinne JO
Genotypes of catechol-O-methyltransferase and response to levodopa treatment in patients with Parkinson's disease.
Neurosci Lett. 2001 Feb 2;298(2):131-4. PubMed: 11163295PAPER Leighton PW, Le Couteur DG, Pang CC, McCann SJ, Chan D, Law LK, Kay R, Pond SM, Woo J
The dopamine transporter gene and Parkinson's disease in a Chinese population.
Neurology. 1997 Dec;49(6):1577-9. PubMed: 9409349PAPER Le Couteur DG, Leighton PW, McCann SJ, Pond S
Association of a polymorphism in the dopamine-transporter gene with Parkinson's disease.
Mov Disord. 1997 Sep;12(5):760-3. PubMed: 9380062PAPER Kurth MC, Kurth JH
Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease.
Am J Med Genet. 1993 Oct 15;48(3):166-8. PubMed: 8291573PAPER Kunugi H, Nanko S, Ueki A, Otsuka E, Hattori M, Hoda F, Vallada HP, Arranz MJ, Collier DA
High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease.
Neurosci Lett. 1997 Jan 17;221(2-3):202-4. PubMed: 9121699PAPER Antonacci R, Perkins AB, Hillstrom M, Tung GA
General case of the day. Perforated Barrett ulcer of the distal esophagus.
Radiographics. 1996 Jan;16(1):197-9. PubMed: 10946700PAPER Kösel S, Lücking CB, Egensperger R, Mehraein P, Graeber MB
Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism.
J Neurosci Res. 1996 Apr 15;44(2):174-83. PubMed: 8723226PAPER Kondo I, Yamamoto M
Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease.
Brain Res. 1998 Sep 28;806(2):271-3. PubMed: 9739148PAPER Kondo I, Kanazawa I
Debrisoquine hydroxylase and Parkinson's disease.
Adv Neurol. 1993;60:338-42. PubMed: 8420147PAPER Koller WC, Glatt SL, Hubble JP, Paolo A, Tröster AI, Handler MS, Horvat RT, Martin C, Schmidt K, Karst A
Apolipoprotein E genotypes in Parkinson's disease with and without dementia.
Ann Neurol. 1995 Feb;37(2):242-5. PubMed: 7847865PAPER Kimura M, Matsushita S, Arai H, Takeda A, Higuchi S
No evidence of association between a dopamine transporter gene polymorphism (1215A/G) and Parkinson's disease.
Ann Neurol. 2001 Feb;49(2):276-7. PubMed: 11220753Current Filters
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