Hagenah J - Search Results

1

Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia.

Zühlke C, Hellenbroich Y, Dalski A, Kononowa N, Hagenah J, Vieregge P, Riess O, Klein C, Schwinger E. Zühlke C, et al. Among authors: hagenah j. Eur J Hum Genet. 2001 Mar;9(3):160-4. doi: 10.1038/sj.ejhg.5200617. Eur J Hum Genet. 2001. PMID: 11313753

2

Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).

Hübner J, Sprenger A, Klein C, Hagenah J, Rambold H, Zühlke C, Kömpf D, Rolfs A, Kimmig H, Helmchen C. Hübner J, et al. Among authors: hagenah j. Neurology. 2007 Sep 11;69(11):1160-8. doi: 10.1212/01.wnl.0000276958.91986.89. Neurology. 2007. PMID: 17846415

3

Radiculopathy and myelopathy in patients with primary cervical dystonia.

Hagenah JM, Vieregge A, Vieregge P. Hagenah JM, et al. Eur Neurol. 2001;45(4):236-40. doi: 10.1159/000052135. Eur Neurol. 2001. PMID: 11385261

4

Focal and segmental primary dystonia in north-western Germany--a clinico-genetic study.

Maniak S, Sieberer M, Hagenah J, Klein C, Vieregge P. Maniak S, et al. Among authors: hagenah j. Acta Neurol Scand. 2003 Mar;107(3):228-32. doi: 10.1034/j.1600-0404.2003.01362.x. Acta Neurol Scand. 2003. PMID: 12614318

5

Search for a founder mutation in idiopathic focal dystonia from Northern Germany.

Klein C, Ozelius LJ, Hagenah J, Breakefield XO, Risch NJ, Vieregge P. Klein C, et al. Among authors: hagenah j. Am J Hum Genet. 1998 Dec;63(6):1777-82. doi: 10.1086/302143. Am J Hum Genet. 1998. PMID: 9837831 Free PMC article.

6

Exogenous levodopa is not toxic to elderly subjects with non-parkinsonian movement disorders: further clinical evidence.

Hagenah J, Klein C, Sieberer M, Vieregge P. Hagenah J, et al. J Neural Transm (Vienna). 1999;106(3-4):301-7. doi: 10.1007/s007020050159. J Neural Transm (Vienna). 1999. PMID: 10392538

7

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

8

Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia.

Klein C, Hedrich K, Kabakçi K, Mohrmann K, Wiegers K, Landt O, Hagenah J, Schwinger E, Pramstaller PP, Ozelius LJ, Gucuyener K, Aysun S, Demir E. Klein C, et al. Among authors: hagenah j. Neurology. 2002 Dec 10;59(11):1783-6. doi: 10.1212/01.wnl.0000035629.04791.3f. Neurology. 2002. PMID: 12473771

9

Mutations in DYT1: extension of the phenotypic and mutational spectrum.

Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, Hagenah J, Garrels J, Witt K, Klostermann F, Svetel M, Friedman J, Kostic V, Bressman SB, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Kabakci K, et al. Among authors: hagenah j. Neurology. 2004 Feb 10;62(3):395-400. doi: 10.1212/01.wnl.0000113024.84178.f7. Neurology. 2004. PMID: 14872019

10

Autosomal dominant Parkinson's disease in a large German pedigree.

Brüggemann N, Külper W, Hagenah J, Bauer P, Pattaro C, Tadic V, Lohnau T, Winkler S, Tönnies H, Sprenger A, Pramstaller P, Rolfs A, Siebert R, Riess O, Vieregge P, Lohmann K, Klein C. Brüggemann N, et al. Among authors: hagenah j. Acta Neurol Scand. 2012 Aug;126(2):129-37. doi: 10.1111/j.1600-0404.2011.01621.x. Epub 2011 Nov 23. Acta Neurol Scand. 2012. PMID: 22107061

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