Schöls L - Search Results

1

Speech treatment improves dysarthria in multisystemic ataxia: a rater-blinded, controlled pilot-study in ARSACS.

Vogel AP, Stoll LH, Oettinger A, Rommel N, Kraus EM, Timmann D, Scott D, Atay C, Storey E, Schöls L, Synofzik M. Vogel AP, et al. Among authors: schols l. J Neurol. 2019 May;266(5):1260-1266. doi: 10.1007/s00415-019-09258-4. Epub 2019 Mar 6. J Neurol. 2019. PMID: 30840144

2

Motor cortex activation by transcranial magnetic stimulation in ataxia patients depends on the genetic defect.

Schwenkreis P, Tegenthoff M, Witscher K, Börnke C, Przuntek H, Malin JP, Schöls L. Schwenkreis P, et al. Among authors: schols l. Brain. 2002 Feb;125(Pt 2):301-9. doi: 10.1093/brain/awf023. Brain. 2002. PMID: 11844730

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. Among authors: schols l. Ann Neurol. 2003 Sep;54(3):367-75. doi: 10.1002/ana.10676. Ann Neurol. 2003. PMID: 12953269

4

"Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2).

Schöls L, Arning L, Schüle R, Epplen JT, Timmann D. Schöls L, et al. J Neurol. 2008 Apr;255(4):495-501. doi: 10.1007/s00415-008-0707-z. Epub 2008 Mar 20. J Neurol. 2008. PMID: 18350359

5

Spinal cord atrophy in spinocerebellar ataxia type 3 and 6 : impact on clinical disability.

Lukas C, Hahn HK, Bellenberg B, Hellwig K, Globas C, Schimrigk SK, Köster O, Schöls L. Lukas C, et al. Among authors: schols l. J Neurol. 2008 Aug;255(8):1244-9. doi: 10.1007/s00415-008-0907-6. Epub 2008 Jun 5. J Neurol. 2008. PMID: 18506570

6

Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).

Arning L, Schöls L, Cin H, Souquet M, Epplen JT, Timmann D. Arning L, et al. Among authors: schols l. Neurogenetics. 2008 Oct;9(4):295-9. doi: 10.1007/s10048-008-0139-z. Epub 2008 Jul 29. Neurogenetics. 2008. PMID: 18663494

7

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

Globas C, du Montcel ST, Baliko L, Boesch S, Depondt C, DiDonato S, Durr A, Filla A, Klockgether T, Mariotti C, Melegh B, Rakowicz M, Ribai P, Rola R, Schmitz-Hubsch T, Szymanski S, Timmann D, Van de Warrenburg BP, Bauer P, Schols L. Globas C, et al. Among authors: schols l. Mov Disord. 2008 Nov 15;23(15):2232-8. doi: 10.1002/mds.22288. Mov Disord. 2008. PMID: 18759344

8

Comparison of three clinical rating scales in Friedreich ataxia (FRDA).

Bürk K, Mälzig U, Wolf S, Heck S, Dimitriadis K, Schmitz-Hübsch T, Hering S, Lindig TM, Haug V, Timmann D, Degen I, Kruse B, Dörr JM, Ratzka S, Ivo A, Schöls L, Boesch S, Klockgether T, Klopstock T, Schulz JB. Bürk K, et al. Among authors: schols l. Mov Disord. 2009 Sep 15;24(12):1779-84. doi: 10.1002/mds.22660. Mov Disord. 2009. PMID: 19562766

9

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

Schulz JB, Borkert J, Wolf S, Schmitz-Hübsch T, Rakowicz M, Mariotti C, Schöls L, Timmann D, van de Warrenburg B, Dürr A, Pandolfo M, Kang JS, Mandly AG, Nägele T, Grisoli M, Boguslawska R, Bauer P, Klockgether T, Hauser TK. Schulz JB, et al. Among authors: schols l. Neuroimage. 2010 Jan 1;49(1):158-68. doi: 10.1016/j.neuroimage.2009.07.027. Epub 2009 Jul 22. Neuroimage. 2010. PMID: 19631275

10

Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations.

Schulte C, Synofzik M, Gasser T, Schöls L. Schulte C, et al. Among authors: schols l. Neurology. 2009 Sep 15;73(11):898-900. doi: 10.1212/WNL.0b013e3181b78488. Neurology. 2009. PMID: 19752458 No abstract available.

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