Schüle R - Search Results

1

A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor.

Pomper JK, Wilhelm H, Tayebati SK, Asmus F, Schüle R, Sievert KD, Haensch CA, Melms A, Haarmeier T. Pomper JK, et al. Among authors: schule r. Neurology. 2011 Feb 1;76(5):451-5. doi: 10.1212/WNL.0b013e31820a0a75. Neurology. 2011. PMID: 21282591

2

Second primary tumor in anti-Ma1/2-positive paraneoplastic limbic encephalitis.

Leyhe T, Schüle R, Schwärzler F, Gasser T, Haarmeier T. Leyhe T, et al. Among authors: schule r. J Neurooncol. 2006 May;78(1):49-51. doi: 10.1007/s11060-005-9052-6. Epub 2005 Nov 29. J Neurooncol. 2006. PMID: 16314942

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. Neurology. 2006 Aug 8;67(3):430-4. doi: 10.1212/01.wnl.0000228242.53336.90. Neurology. 2006. PMID: 16894103

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. Among authors: schule r. 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

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. Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8. Neurology. 2009. PMID: 19357379

6

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: schule r. Neurology. 2011 Sep 6;77(10):959-64. doi: 10.1212/WNL.0b013e31822e0479. Epub 2011 Aug 10. Neurology. 2011. PMID: 21832227

7

De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).

Karle KN, Biskup S, Schüle R, Schweitzer KJ, Krüger R, Bauer P, Bender B, Nägele T, Schöls L. Karle KN, et al. Among authors: schule r. Neurology. 2013 Dec 3;81(23):2039-44. doi: 10.1212/01.wnl.0000436945.01023.ac. Epub 2013 Nov 6. Neurology. 2013. PMID: 24198292

8

PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.

Synofzik M, Gonzalez MA, Lourenco CM, Coutelier M, Haack TB, Rebelo A, Hannequin D, Strom TM, Prokisch H, Kernstock C, Durr A, Schöls L, Lima-Martínez MM, Farooq A, Schüle R, Stevanin G, Marques W Jr, Züchner S. Synofzik M, et al. Among authors: schule r. Brain. 2014 Jan;137(Pt 1):69-77. doi: 10.1093/brain/awt326. Epub 2013 Dec 19. Brain. 2014. PMID: 24355708 Free PMC article.

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: schule r. 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

Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier.

Bonifert T, Karle KN, Tonagel F, Batra M, Wilhelm C, Theurer Y, Schoenfeld C, Kluba T, Kamenisch Y, Carelli V, Wolf J, Gonzalez MA, Speziani F, Schüle R, Züchner S, Schöls L, Wissinger B, Synofzik M. Bonifert T, et al. Among authors: schule r. Brain. 2014 Aug;137(Pt 8):2164-77. doi: 10.1093/brain/awu165. Epub 2014 Jun 25. Brain. 2014. PMID: 24970096 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

322 results

Search Page