Hagenah J - Search Results

1

Association studies of Parkinson's disease and parkin polymorphisms.

Klein C, Schumacher K, Jacobs H, Hagenah J, Kis B, Garrels J, Schwinger E, Ozelius L, Pramstaller P, Vieregge P, Kramer PL. Klein C, et al. Among authors: hagenah j. Ann Neurol. 2000 Jul;48(1):126-7. Ann Neurol. 2000. PMID: 10894229 No abstract available.

2

Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles.

Hagenah JM, König IR, Becker B, Hilker R, Kasten M, Hedrich K, Pramstaller PP, Klein C, Seidel G. Hagenah JM, et al. J Neurol. 2007 Oct;254(10):1407-13. doi: 10.1007/s00415-007-0567-y. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934880

3

Parkinson's disease in twins: a follow-up study.

Vieregge P, Hagenah J, Heberlein I, Klein C, Ludin HP. Vieregge P, et al. Among authors: hagenah j. Neurology. 1999 Aug 11;53(3):566-72. doi: 10.1212/wnl.53.3.566. Neurology. 1999. PMID: 10449122

4

Neuropsychological abnormalities in first degree relatives of patients with familial Parkinson's disease.

Kis B, Heberlein I, Hagenah J, Jacobs H, Klein C, Vieregge P. Kis B, et al. Among authors: hagenah j. J Neurol Neurosurg Psychiatry. 2000 Dec;69(6):838. doi: 10.1136/jnnp.69.6.838. J Neurol Neurosurg Psychiatry. 2000. PMID: 11185648 Free PMC article. No abstract available.

5

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

Binkofski F, Reetz K, Gaser C, Hilker R, Hagenah J, Hedrich K, van Eimeren T, Thiel A, Büchel C, Pramstaller PP, Siebner HR, Klein C. Binkofski F, et al. Among authors: hagenah j. Neurology. 2007 Aug 28;69(9):842-50. doi: 10.1212/01.wnl.0000267844.72421.6c. Neurology. 2007. PMID: 17724286

6

Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS study.

Bäumer T, Pramstaller PP, Siebner HR, Schippling S, Hagenah J, Peller M, Gerloff C, Klein C, Münchau A. Bäumer T, et al. Among authors: hagenah j. Neurology. 2007 Nov 20;69(21):1976-81. doi: 10.1212/01.wnl.0000278109.76607.0a. Neurology. 2007. PMID: 18025391

7

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.

van Nuenen BF, Weiss MM, Bloem BR, Reetz K, van Eimeren T, Lohmann K, Hagenah J, Pramstaller PP, Binkofski F, Klein C, Siebner HR. van Nuenen BF, et al. Among authors: hagenah j. Neurology. 2009 Mar 24;72(12):1041-7. doi: 10.1212/01.wnl.0000338699.56379.11. Epub 2008 Nov 26. Neurology. 2009. PMID: 19038850 Free PMC article.

8

Transdermal nicotine in PD: a randomized, double-blind, placebo-controlled study.

Vieregge A, Sieberer M, Jacobs H, Hagenah JM, Vieregge P. Vieregge A, et al. Among authors: hagenah jm. Neurology. 2001 Sep 25;57(6):1032-5. doi: 10.1212/wnl.57.6.1032. Neurology. 2001. PMID: 11571330 Clinical Trial.

9

Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany.

Klein C, Vieregge P, Hagenah J, Sieberer M, Doyle E, Jacobs H, Gasser T, Breakefield XO, Risch NJ, Ozelius LJ. Klein C, et al. Among authors: hagenah j. Ann Hum Genet. 1999 Jul;63(Pt 4):285-91. doi: 10.1046/j.1469-1809.1999.6340285.x. Ann Hum Genet. 1999. PMID: 10738540

10

Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism.

Buhmann C, Binkofski F, Klein C, Büchel C, van Eimeren T, Erdmann C, Hedrich K, Kasten M, Hagenah J, Deuschl G, Pramstaller PP, Siebner HR. Buhmann C, et al. Among authors: hagenah j. Brain. 2005 Oct;128(Pt 10):2281-90. doi: 10.1093/brain/awh572. Epub 2005 Jun 9. Brain. 2005. PMID: 15947065

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