Müller U - Search Results

1

Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany.

Waibel S, Neumann M, Rosenbohm A, Birve A, Volk AE, Weishaupt JH, Meyer T, Müller U, Andersen PM, Ludolph AC. Waibel S, et al. Among authors: muller u. Eur J Neurol. 2013 Mar;20(3):540-546. doi: 10.1111/ene.12031. Epub 2012 Dec 6. Eur J Neurol. 2013. PMID: 23217123

2

Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis.

Kress JA, Kühnlein P, Winter P, Ludolph AC, Kassubek J, Müller U, Sperfeld AD. Kress JA, et al. Among authors: muller u. Ann Neurol. 2005 Nov;58(5):800-3. doi: 10.1002/ana.20665. Ann Neurol. 2005. PMID: 16240357

3

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.

Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T. Neubauer BA, et al. Among authors: muller u. Neurology. 2008 Jul 15;71(3):177-83. doi: 10.1212/01.wnl.0000317090.92185.ec. Neurology. 2008. PMID: 18625963

4

Cancer and neurodegeneration: Time to move beyond Janus?

Tallaksen CM, Müller U. Tallaksen CM, et al. Among authors: muller u. Neurology. 2017 Mar 21;88(12):1106-1107. doi: 10.1212/WNL.0000000000003727. Epub 2017 Feb 15. Neurology. 2017. PMID: 28202693 No abstract available.

5

Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.

Kamm C, Asmus F, Mueller J, Mayer P, Sharma M, Muller UJ, Beckert S, Ehling R, Illig T, Wichmann HE, Poewe W, Mueller JC, Gasser T. Kamm C, et al. Among authors: muller uj. Neurology. 2006 Nov 28;67(10):1857-9. doi: 10.1212/01.wnl.0000244423.63406.17. Neurology. 2006. PMID: 17130424

6

Severe cutaneous Candida infection during natalizumab therapy in multiple sclerosis.

Gutwinski S, Erbe S, Münch C, Janke O, Müller U, Haas J. Gutwinski S, et al. Among authors: muller u. Neurology. 2010 Feb 9;74(6):521-3. doi: 10.1212/WNL.0b013e3181cef810. Neurology. 2010. PMID: 20142621 No abstract available.

7

Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern Europe.

Verschuuren-Bemelmans CC, Winter P, Sival DA, Elting JW, Brouwer OF, Müller U. Verschuuren-Bemelmans CC, et al. Among authors: muller u. Eur J Hum Genet. 2008 Nov;16(11):1407-11. doi: 10.1038/ejhg.2008.108. Epub 2008 Jun 4. Eur J Hum Genet. 2008. PMID: 18523452

8

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?

Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM. Waters MF, et al. Among authors: muller u. Neurology. 2005 Oct 11;65(7):1111-3. doi: 10.1212/01.wnl.0000177490.05162.41. Epub 2005 Aug 31. Neurology. 2005. PMID: 16135769

9

Rational therapeutic approaches to progressive supranuclear palsy.

Stamelou M, de Silva R, Arias-Carrión O, Boura E, Höllerhage M, Oertel WH, Müller U, Höglinger GU. Stamelou M, et al. Among authors: muller u. Brain. 2010 Jun;133(Pt 6):1578-90. doi: 10.1093/brain/awq115. Epub 2010 May 14. Brain. 2010. PMID: 20472654 Review.

10

SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.

Ebach K, Joos H, Doose H, Stephani U, Kurlemann G, Fiedler B, Hahn A, Hauser E, Hundt K, Holthausen H, Müller U, Neubauer BA. Ebach K, et al. Among authors: muller u. Neuropediatrics. 2005 Jun;36(3):210-3. doi: 10.1055/s-2005-865607. Neuropediatrics. 2005. PMID: 15944908 Free article.

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