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71 results

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Page 1
A diagnostic conundrum.
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: carr as. 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.
An observational study of asymmetry in CMT1A.
Pelayo-Negro AL, Carr AS, Laura M, Skorupinska M, Reilly MM. Pelayo-Negro AL, et al. Among authors: carr as. J Neurol Neurosurg Psychiatry. 2015 May;86(5):589-90. doi: 10.1136/jnnp-2014-309096. Epub 2014 Oct 13. J Neurol Neurosurg Psychiatry. 2015. PMID: 25313262 Free PMC article. No abstract available.
MFN2 deletion of exons 7 and 8: founder mutation in the UK population.
Carr AS, Polke JM, Wilson J, Pelayo-Negro AL, Laura M, Nanji T, Holt J, Vaughan J, Rankin J, Sweeney MG, Blake J, Houlden H, Reilly MM. Carr AS, et al. J Peripher Nerv Syst. 2015 Jun;20(2):67-71. doi: 10.1111/jns.12117. J Peripher Nerv Syst. 2015. PMID: 26114802
A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK.
Carr AS, Pelayo-Negro AL, Evans MR, Laurà M, Blake J, Stancanelli C, Iodice V, Wechalekar AD, Whelan CJ, Gillmore JD, Hawkins PN, Reilly MM. Carr AS, et al. J Neurol Neurosurg Psychiatry. 2016 Jun;87(6):620-7. doi: 10.1136/jnnp-2015-310907. Epub 2015 Aug 4. J Neurol Neurosurg Psychiatry. 2016. PMID: 26243339
Peripheral neuropathy in complex inherited diseases: an approach to diagnosis.
Rossor AM, Carr AS, Devine H, Chandrashekar H, Pelayo-Negro AL, Pareyson D, Shy ME, Scherer SS, Reilly MM. Rossor AM, et al. Among authors: carr as. J Neurol Neurosurg Psychiatry. 2017 Oct;88(10):846-863. doi: 10.1136/jnnp-2016-313960. Epub 2017 Aug 9. J Neurol Neurosurg Psychiatry. 2017. PMID: 28794150 Free article. Review.
POEMS neuropathy: optimising diagnosis and management.
Keddie S, D'Sa S, Foldes D, Carr AS, Reilly MM, Lunn MPT. Keddie S, et al. Among authors: carr as. Pract Neurol. 2018 Aug;18(4):278-290. doi: 10.1136/practneurol-2017-001792. Epub 2018 Mar 6. Pract Neurol. 2018. PMID: 29511110 Free article. Review.
Spinal Stenosis in Familial Transthyretin Amyloidosis.
Carr AS, Shah S, Choi D, Blake J, Phadke R, Gilbertson J, Whelan CJ, Wechalekar AD, Gillmore JD, Hawkins PN, Reilly MM. Carr AS, et al. J Neuromuscul Dis. 2019;6(2):267-270. doi: 10.3233/JND-180348. J Neuromuscul Dis. 2019. PMID: 30856118
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre.
Bugiardini E, Khan AM, Phadke R, Lynch DS, Cortese A, Feng L, Gang Q, Pittman AM, Morrow JM, Turner C, Carr AS, Quinlivan R, Rossor AM, Holton JL, Parton M, Blake JC, Reilly MM, Houlden H, Matthews E, Hanna MG. Bugiardini E, et al. Among authors: carr as. Neuromuscul Disord. 2019 Oct;29(10):747-757. doi: 10.1016/j.nmd.2019.08.003. Epub 2019 Aug 19. Neuromuscul Disord. 2019. PMID: 31561939
71 results