Schöls L - Search Results

1

"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers.

Rattay TW, Schöls L, Zeltner L, Rohrschneider WK, Ernemann U, Lindig T. Rattay TW, et al. Among authors: schols l. J Neurol. 2022 Nov;269(11):6148-6151. doi: 10.1007/s00415-022-11198-5. Epub 2022 May 25. J Neurol. 2022. PMID: 35614164 No abstract available.

2

Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia.

Schulte T, Miterski B, Börnke C, Przuntek H, Epplen JT, Schöls L. Schulte T, et al. Among authors: schols l. Neurology. 2003 May 13;60(9):1529-32. doi: 10.1212/01.wnl.0000058769.75218.69. Neurology. 2003. PMID: 12743246

3

The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity.

Schüle R, Holland-Letz T, Klimpe S, Kassubek J, Klopstock T, Mall V, Otto S, Winner B, Schöls L. Schüle R, et al. Among authors: schols l. Neurology. 2006 Aug 8;67(3):430-4. doi: 10.1212/01.wnl.0000228242.53336.90. Neurology. 2006. PMID: 16894103

4

SPG10 is a rare cause of spastic paraplegia in European families.

Schüle R, Kremer BP, Kassubek J, Auer-Grumbach M, Kostic V, Klopstock T, Klimpe S, Otto S, Boesch S, van de Warrenburg BP, Schöls L. Schüle R, et al. Among authors: schols l. J Neurol Neurosurg Psychiatry. 2008 May;79(5):584-7. doi: 10.1136/jnnp.2007.137596. Epub 2008 Feb 1. J Neurol Neurosurg Psychiatry. 2008. PMID: 18245137 Free article.

5

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.

Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L. Schüle R, et al. Among authors: schols l. Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8. Neurology. 2009. PMID: 19357379

6

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.

Schüle R, Schlipf N, Synofzik M, Klebe S, Klimpe S, Hehr U, Winner B, Lindig T, Dotzer A, Riess O, Winkler J, Schöls L, Bauer P. Schüle R, et al. Among authors: schols l. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1402-4. doi: 10.1136/jnnp.2008.167528. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917823

7

EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.

Gasser T, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, Zeviani M, Burgunder JM, Harbo HF; EFNS. Gasser T, et al. Among authors: schols l. Eur J Neurol. 2010 Feb;17(2):179-88. doi: 10.1111/j.1468-1331.2009.02873.x. Epub 2009 Dec 28. Eur J Neurol. 2010. PMID: 20050888

8

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.

Weber YG, Kamm C, Suls A, Kempfle J, Kotschet K, Schüle R, Wuttke TV, Maljevic S, Liebrich J, Gasser T, Ludolph AC, Van Paesschen W, Schöls L, De Jonghe P, Auburger G, Lerche H. Weber YG, et al. Among authors: schols l. Neurology. 2011 Sep 6;77(10):959-64. doi: 10.1212/WNL.0b013e31822e0479. Epub 2011 Aug 10. Neurology. 2011. PMID: 21832227

9

Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients.

Müller vom Hagen J, Karle KN, Schüle R, Krägeloh-Mann I, Schöls L. Müller vom Hagen J, et al. Among authors: schols l. Eur J Neurol. 2014 Jul;21(7):983-8. doi: 10.1111/ene.12423. Epub 2014 Apr 2. Eur J Neurol. 2014. PMID: 24698313

10

CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegia.

Kariminejad A, Schöls L, Schüle R, Tonekaboni SH, Abolhassani A, Fadaee M, Rosti RO, Gleeson JG. Kariminejad A, et al. Among authors: schols l. Eur J Paediatr Neurol. 2016 Sep;20(5):782-7. doi: 10.1016/j.ejpn.2016.05.013. Epub 2016 Jun 2. Eur J Paediatr Neurol. 2016. PMID: 27292318 Free PMC article.

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