Rolfs A - Search Results

1

A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

Westenberger A, Reyes CJ, Saranza G, Dobricic V, Hanssen H, Domingo A, Laabs BH, Schaake S, Pozojevic J, Rakovic A, Grütz K, Begemann K, Walter U, Dressler D, Bauer P, Rolfs A, Münchau A, Kaiser FJ, Ozelius LJ, Jamora RD, Rosales RL, Diesta CCE, Lohmann K, König IR, Brüggemann N, Klein C. Westenberger A, et al. Among authors: rolfs a. Ann Neurol. 2019 Jun;85(6):812-822. doi: 10.1002/ana.25488. Epub 2019 May 3. Ann Neurol. 2019. PMID: 30973967

2

Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.

Bauer I, Gencik M, Laccone F, Peters H, Weber BH, Feder EH, Weirich H, Morris-Rosendahl DJ, Rolfs A, Gencikova A, Bauer P, Wenning GK, Epplen JT, Holmes SE, Margolis RL, Ross CA, Riess O. Bauer I, et al. Among authors: rolfs a. Ann Neurol. 2002 May;51(5):662. doi: 10.1002/ana.10184. Ann Neurol. 2002. PMID: 12112122 No abstract available.

3

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

Rolfs A, Koeppen AH, Bauer I, Bauer P, Buhlmann S, Topka H, Schöls L, Riess O. Rolfs A, et al. Ann Neurol. 2003 Sep;54(3):367-75. doi: 10.1002/ana.10676. Ann Neurol. 2003. PMID: 12953269

4

Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study.

Rolfs A, Böttcher T, Zschiesche M, Morris P, Winchester B, Bauer P, Walter U, Mix E, Löhr M, Harzer K, Strauss U, Pahnke J, Grossmann A, Benecke R. Rolfs A, et al. Lancet. 2005 Nov 19;366(9499):1794-6. doi: 10.1016/S0140-6736(05)67635-0. Lancet. 2005. PMID: 16298216

5

Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach.

Tomiuk J, Bachmann L, Bauer C, Rolfs A, Schöls L, Roos C, Zischler H, Schuler MM, Bruntner S, Riess O, Bauer P. Tomiuk J, et al. Among authors: rolfs a. Eur J Hum Genet. 2007 Jan;15(1):81-7. doi: 10.1038/sj.ejhg.5201721. Epub 2006 Oct 11. Eur J Hum Genet. 2007. PMID: 17033685

6

Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.

Hehr U, Bauer P, Winner B, Schule R, Olmez A, Koehler W, Uyanik G, Engel A, Lenz D, Seibel A, Hehr A, Ploetz S, Gamez J, Rolfs A, Weis J, Ringer TM, Bonin M, Schuierer G, Marienhagen J, Bogdahn U, Weber BH, Topaloglu H, Schols L, Riess O, Winkler J. Hehr U, et al. Among authors: rolfs a. Ann Neurol. 2007 Dec;62(6):656-65. doi: 10.1002/ana.21310. Ann Neurol. 2007. PMID: 18067136

7

Specific properties of sodium currents in multipotent striatal progenitor cells.

Wasner U, Geist B, Battefeld A, Bauer P, Müller J, Rolfs A, Strauss U. Wasner U, et al. Among authors: rolfs a. Eur J Neurosci. 2008 Sep;28(6):1068-79. doi: 10.1111/j.1460-9568.2008.06427.x. Epub 2008 Sep 9. Eur J Neurosci. 2008. PMID: 18783365

8

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Reetz K, Lencer R, Hagenah JM, Gaser C, Tadic V, Walter U, Wolters A, Steinlechner S, Zühlke C, Brockmann K, Klein C, Rolfs A, Binkofski F. Reetz K, et al. Among authors: rolfs a. Cerebellum. 2010 Jun;9(2):210-7. doi: 10.1007/s12311-009-0150-4. Cerebellum. 2010. PMID: 20016963

9

CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM study.

Reetz K, Kleiman A, Klein C, Lencer R, Zuehlke C, Brockmann K, Rolfs A, Binkofski F. Reetz K, et al. Among authors: rolfs a. PLoS One. 2011 Jan 19;6(1):e15125. doi: 10.1371/journal.pone.0015125. PLoS One. 2011. PMID: 21311576 Free PMC article.

10

Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation.

Fong CY, Rolfs A, Schwarzbraun T, Klein C, O'Callaghan FJ. Fong CY, et al. Among authors: rolfs a. Eur J Paediatr Neurol. 2011 May;15(3):271-5. doi: 10.1016/j.ejpn.2011.01.001. Epub 2011 Feb 12. Eur J Paediatr Neurol. 2011. PMID: 21316993

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