Brandner S - Search Results

1

Keddie S, Jaunmuktane Z, Brandner S, Shah S, Maddison P, Rees JH, Hanna MG, Lunn MPT, Reilly MM, Rossor AM, Carr AS. Keddie S, et al. Among authors: brandner s. Pract Neurol. 2018 Apr;18(2):137-142. doi: 10.1136/practneurol-2017-001801. Epub 2018 Jan 23. Pract Neurol. 2018. PMID: 29363556 Free PMC article.

2

Rituximab in the treatment of three coexistent neurological autoimmune diseases: chronic inflammatory demyelinating polyradiculoneuropathy, Morvan syndrome and myasthenia gravis.

Sadnicka A, Reilly MM, Mummery C, Brandner S, Hirsch N, Lunn MP. Sadnicka A, et al. Among authors: brandner s. J Neurol Neurosurg Psychiatry. 2011 Feb;82(2):230-2. doi: 10.1136/jnnp.2009.174888. Epub 2010 May 12. J Neurol Neurosurg Psychiatry. 2011. PMID: 20462915

3

Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases.

Siddique D, Hyare H, Wroe S, Webb T, Macfarlane R, Rudge P, Collinge J, Powell C, Brandner S, So PW, Walker S, Mead S, Yousry T, Thornton JS. Siddique D, et al. Among authors: brandner s. Brain. 2010 Oct;133(10):3058-68. doi: 10.1093/brain/awq243. Brain. 2010. PMID: 20881162

4

Mutation in FAM134B causing severe hereditary sensory neuropathy.

Murphy SM, Davidson GL, Brandner S, Houlden H, Reilly MM. Murphy SM, et al. Among authors: brandner s. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):119-20. doi: 10.1136/jnnp.2010.228965. Epub 2010 Nov 28. J Neurol Neurosurg Psychiatry. 2012. PMID: 21115472 Free PMC article.

5

Variable phenotypes are associated with PMP22 missense mutations.

Russo M, Laurá M, Polke JM, Davis MB, Blake J, Brandner S, Hughes RA, Houlden H, Bennett DL, Lunn MP, Reilly MM. Russo M, et al. Among authors: brandner s. Neuromuscul Disord. 2011 Feb;21(2):106-14. doi: 10.1016/j.nmd.2010.11.011. Epub 2010 Dec 30. Neuromuscul Disord. 2011. PMID: 21194947

6

Bortezomib-induced inflammatory neuropathy.

Saifee TA, Elliott KJ, Rabin N, Yong KL, D'Sa S, Brandner S, Lunn MP, Blake J, Reilly MM. Saifee TA, et al. Among authors: brandner s. J Peripher Nerv Syst. 2010 Dec;15(4):366-8. doi: 10.1111/j.1529-8027.2010.00287.x. J Peripher Nerv Syst. 2010. PMID: 21199108 No abstract available.

7

Sarcoidosis presenting as acute inflammatory demyelinating polyradiculoneuropathy.

Saifee TA, Reilly MM, Ako E, Rugg-Gunn F, Brandner S, Lunn MP, Leary SM. Saifee TA, et al. Among authors: brandner s. Muscle Nerve. 2011 Feb;43(2):296-8. doi: 10.1002/mus.21890. Muscle Nerve. 2011. PMID: 21254101 No abstract available.

8

A novel mutation in the nerve-specific 5'UTR of the GJB1 gene causes X-linked Charcot-Marie-Tooth disease.

Murphy SM, Polke J, Manji H, Blake J, Reiniger L, Sweeney M, Houlden H, Brandner S, Reilly MM. Murphy SM, et al. Among authors: brandner s. J Peripher Nerv Syst. 2011 Mar;16(1):65-70. doi: 10.1111/j.1529-8027.2011.00321.x. J Peripher Nerv Syst. 2011. PMID: 21504505

9

c-Jun expression in human neuropathies: a pilot study.

Hutton EJ, Carty L, Laurá M, Houlden H, Lunn MP, Brandner S, Mirsky R, Jessen K, Reilly MM. Hutton EJ, et al. Among authors: brandner s. J Peripher Nerv Syst. 2011 Dec;16(4):295-303. doi: 10.1111/j.1529-8027.2011.00360.x. J Peripher Nerv Syst. 2011. PMID: 22176144

10

BAG3 mutations: another cause of giant axonal neuropathy.

Jaffer F, Murphy SM, Scoto M, Healy E, Rossor AM, Brandner S, Phadke R, Selcen D, Jungbluth H, Muntoni F, Reilly MM. Jaffer F, et al. Among authors: brandner s. J Peripher Nerv Syst. 2012 Jun;17(2):210-6. doi: 10.1111/j.1529-8027.2012.00409.x. J Peripher Nerv Syst. 2012. PMID: 22734908

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

457 results

Search Page

Filters