Schöls L - Search Results

1

A standardised protocol for blood and cerebrospinal fluid collection and processing for biomarker research in ataxia.

Santana MM, Gaspar LS, Pinto MM, Silva P, Adão D, Pereira D, Ribeiro JA, Cunha I, Huebener-Schmid J, Raposo M, Ferreira AF, Faber J, Kuhs S, Garcia-Moreno H, Reetz K, Thieme A, Infante J, van de Warrenburg BPC, Giunti P, Riess O, Schöls L, Lima M, Klockgether T, Januário C, de Almeida LP; European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative Study Group. Santana MM, et al. Among authors: schols l. Neuropathol Appl Neurobiol. 2023 Apr;49(2):e12892. doi: 10.1111/nan.12892. Neuropathol Appl Neurobiol. 2023. PMID: 36798010 Free PMC article.

2

Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.

Schöls L, Vieira-Saecker AM, Schöls S, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: schols s. Hum Mol Genet. 1995 Jun;4(6):1001-5. doi: 10.1093/hmg/4.6.1001. Hum Mol Genet. 1995. PMID: 7655453

3

Transmission distortion of the mutant alleles in spinocerebellar ataxia.

Riess O, Epplen JT, Amoiridis G, Przuntek H, Schöls L. Riess O, et al. Among authors: schols l. Hum Genet. 1997 Feb;99(2):282-4. doi: 10.1007/s004390050355. Hum Genet. 1997. PMID: 9048937

4

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

5

An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.

Schmidt T, Landwehrmeyer GB, Schmitt I, Trottier Y, Auburger G, Laccone F, Klockgether T, Völpel M, Epplen JT, Schöls L, Riess O. Schmidt T, et al. Among authors: schols l. Brain Pathol. 1998 Oct;8(4):669-79. doi: 10.1111/j.1750-3639.1998.tb00193.x. Brain Pathol. 1998. PMID: 9804376 Free PMC article.

6

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

7

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.

8

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

9

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

10

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

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