Schöls L - Search Results

1

Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3.

Garcia-Moreno H, Prudencio M, Thomas-Black G, Solanky N, Jansen-West KR, Hanna Al-Shaikh R, Heslegrave A, Zetterberg H, Santana MM, Pereira de Almeida L, Vasconcelos-Ferreira A, Januário C, Infante J, Faber J, Klockgether T, Reetz K, Raposo M, Ferreira AF, Lima M, Schöls L, Synofzik M, Hübener-Schmid J, Puschmann A, Gorcenco S, Wszolek ZK, Petrucelli L, Giunti P. Garcia-Moreno H, et al. Among authors: schols l. Eur J Neurol. 2022 Aug;29(8):2439-2452. doi: 10.1111/ene.15373. Epub 2022 May 26. Eur J Neurol. 2022. PMID: 35478426 Free PMC article.

2

Repeat length and disease progression in spinocerebellar ataxia type 3.

Klockgether T, Kramer B, Lüdtke R, Schöls L, Laccone F. Klockgether T, et al. Among authors: schols l. Lancet. 1996 Sep 21;348(9030):830. doi: 10.1016/S0140-6736(05)65255-5. Lancet. 1996. PMID: 8814012 No abstract available.

3

The natural history of degenerative ataxia: a retrospective study in 466 patients.

Klockgether T, Lüdtke R, Kramer B, Abele M, Bürk K, Schöls L, Riess O, Laccone F, Boesch S, Lopes-Cendes I, Brice A, Inzelberg R, Zilber N, Dichgans J. Klockgether T, et al. Among authors: schols l. Brain. 1998 Apr;121 ( Pt 4):589-600. doi: 10.1093/brain/121.4.589. Brain. 1998. PMID: 9577387

4

Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?

Schöls L, Haan J, Riess O, Amoiridis G, Przuntek H. Schöls L, et al. Neurology. 1998 Dec;51(6):1603-7. doi: 10.1212/wnl.51.6.1603. Neurology. 1998. PMID: 9855509

5

Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD).

Klockgether T, Schöls L, Abele M, Bürk K, Topka H, Andres F, Amoiridis G, Lüdtke R, Riess O, Laccone F, Dichgans J. Klockgether T, et al. Among authors: schols l. J Neurol Neurosurg Psychiatry. 1999 Feb;66(2):222-4. doi: 10.1136/jnnp.66.2.222. J Neurol Neurosurg Psychiatry. 1999. PMID: 10071104 Free PMC article.

6

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.

Dichgans M, Schöls L, Herzog J, Stevanin G, Weirich-Schwaiger H, Rouleau G, Bürk K, Klockgether T, Zühlke C, Laccone F, Riess O, Gasser T. Dichgans M, et al. Among authors: schols l. Neurology. 1999 Mar 10;52(4):849-51. doi: 10.1212/wnl.52.4.849. Neurology. 1999. PMID: 10078738

7

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions.

Schmidt T, Lindenberg KS, Krebs A, Schöls L, Laccone F, Herms J, Rechsteiner M, Riess O, Landwehrmeyer GB. Schmidt T, et al. Among authors: schols l. Ann Neurol. 2002 Mar;51(3):302-10. doi: 10.1002/ana.10101. Ann Neurol. 2002. PMID: 11891825

8

The aetiology of sporadic adult-onset ataxia.

Abele M, Bürk K, Schöls L, Schwartz S, Besenthal I, Dichgans J, Zühlke C, Riess O, Klockgether T. Abele M, et al. Among authors: schols l. Brain. 2002 May;125(5):961-8. doi: 10.1093/brain/awf107. Brain. 2002. PMID: 11960886

9

Prevalence of antigliadin antibodies in ataxia patients.

Abele M, Schöls L, Schwartz S, Klockgether T. Abele M, et al. Among authors: schols l. Neurology. 2003 May 27;60(10):1674-5. doi: 10.1212/01.wnl.0000069606.82919.04. Neurology. 2003. PMID: 12771263

10

Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3.

Rüb U, Bürk K, Schöls L, Brunt ER, de Vos RA, Diaz GO, Gierga K, Ghebremedhin E, Schultz C, Del Turco D, Mittelbronn M, Auburger G, Deller T, Braak H. Rüb U, et al. Among authors: schols l. Neurology. 2004 Oct 12;63(7):1258-63. doi: 10.1212/01.wnl.0000140498.24112.8c. Neurology. 2004. PMID: 15477548

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