Zühlke C - Search Results

1

Homozygous myotonic dystrophy: clinical findings in two patients and review of the literature.

Zühlke C, Roeder E, Purmann S, Wieczorek D, Curry C, Loustalet C, Hellenbroich Y, Richardt HH, Gillessen-Kaesbach G. Zühlke C, et al. Am J Med Genet A. 2007 Sep 1;143A(17):2058-61. doi: 10.1002/ajmg.a.31772. Am J Med Genet A. 2007. PMID: 17663477 Review. No abstract available.

2

Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles.

Zühlke C, Dalski A, Hellenbroich Y, Bubel S, Schwinger E, Bürk K. Zühlke C, et al. Eur J Hum Genet. 2002 Mar;10(3):204-9. doi: 10.1038/sj.ejhg.5200788. Eur J Hum Genet. 2002. PMID: 11973625

3

Phenotypical variability of expanded alleles in the TATA-binding protein gene. Reduced penetrance in SCA17?

Zühlke C, Gehlken U, Hellenbroich Y, Schwinger E, Bürk K. Zühlke C, et al. J Neurol. 2003 Feb;250(2):161-3. doi: 10.1007/s00415-003-0958-7. J Neurol. 2003. PMID: 12574945

4

Focal dystonia as a presenting sign of spinocerebellar ataxia 17.

Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C. Hagenah JM, et al. Among authors: zuhlke c. Mov Disord. 2004 Feb;19(2):217-20. doi: 10.1002/mds.10600. Mov Disord. 2004. PMID: 14978680

5

Aprataxin mutations are a rare cause of early onset ataxia in Germany.

Habeck M, Zühlke C, Bentele KH, Unkelbach S, Kress W, Bürk K, Schwinger E, Hellenbroich Y. Habeck M, et al. Among authors: zuhlke c. J Neurol. 2004 May;251(5):591-4. doi: 10.1007/s00415-004-0374-7. J Neurol. 2004. PMID: 15164193

6

No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.

Hellenbroich Y, Kaulich M, Opitz S, Schwinger E, Zühlke C. Hellenbroich Y, et al. Among authors: zuhlke c. Psychiatr Genet. 2004 Jun;14(2):61-3. doi: 10.1097/01.ypg.0000128763.69225.77. Psychiatr Genet. 2004. PMID: 15167689

7

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias.

Dalski A, Atici J, Kreuz FR, Hellenbroich Y, Schwinger E, Zühlke C. Dalski A, et al. Among authors: zuhlke c. Eur J Hum Genet. 2005 Jan;13(1):118-20. doi: 10.1038/sj.ejhg.5201286. Eur J Hum Genet. 2005. PMID: 15470364

8

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

Hedrich K, Pramstaller PP, Stübke K, Hiller A, Kabakci K, Purmann S, Kasten M, Scaglione C, Schwinger E, Volkmann J, Kostic V, Vieregge P, Martinelli P, Abbruzzese G, Klein C, Zühlke C. Hedrich K, et al. Among authors: zuhlke c. Mov Disord. 2005 Aug;20(8):1060-2. doi: 10.1002/mds.20512. Mov Disord. 2005. PMID: 15929093

9

Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia.

Bürk K, Bühring U, Schulz JB, Zühlke C, Hellenbroich Y, Dichgans J. Bürk K, et al. Among authors: zuhlke c. Arch Neurol. 2005 Jun;62(6):981-5. doi: 10.1001/archneur.62.6.981. Arch Neurol. 2005. PMID: 15956170

10

Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic.

Hellenbroich Y, Bernard V, Zühlke C. Hellenbroich Y, et al. Among authors: zuhlke c. J Neurol. 2008 Apr;255(4):612-3. doi: 10.1007/s00415-008-0771-4. Epub 2008 Feb 25. J Neurol. 2008. PMID: 18293026 No abstract available.

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