Alexander MD - Search Results

1

Neurophysiological and ophthalmological findings of SPG7-related spastic ataxia: a phenotype study in an Irish cohort.

Bogdanova-Mihaylova P, Chen H, Plapp HM, Gorman C, Alexander MD, McHugh JC, Moran S, Early A, Cassidy L, Lynch T, Murphy SM, Walsh RA. Bogdanova-Mihaylova P, et al. Among authors: alexander md. J Neurol. 2021 Oct;268(10):3897-3907. doi: 10.1007/s00415-021-10507-8. Epub 2021 Mar 27. J Neurol. 2021. PMID: 33774748

2

Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland.

Bansagi B, Antoniadi T, Burton-Jones S, Murphy SM, McHugh J, Alexander M, Wells R, Davies J, Hilton-Jones D, Lochmüller H, Chinnery P, Horvath R. Bansagi B, et al. J Neurol. 2015 Aug;262(8):1899-908. doi: 10.1007/s00415-015-7778-4. Epub 2015 Jun 2. J Neurol. 2015. PMID: 26032230 Free PMC article.

3

SCN9A-associated congenital insensitivity to pain and anosmia in an Irish patient.

Bogdanova-Mihaylova P, Alexander MD, Murphy RP, Murphy SM. Bogdanova-Mihaylova P, et al. Among authors: alexander md. J Peripher Nerv Syst. 2015 Jun;20(2):86-7. doi: 10.1111/jns.12123. J Peripher Nerv Syst. 2015. PMID: 26292973 No abstract available.

4

Waardenburg syndrome: a rare cause of inherited neuropathy due to SOX10 mutation.

Bogdanova-Mihaylova P, Alexander MD, Murphy RPJ, Murphy SM. Bogdanova-Mihaylova P, et al. Among authors: alexander md. J Peripher Nerv Syst. 2017 Sep;22(3):219-223. doi: 10.1111/jns.12221. J Peripher Nerv Syst. 2017. PMID: 28544110

5

Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family.

Bogdanova-Mihaylova P, Murphy RPJ, Alexander MD, McHugh JC, Foley AR, Brett F, Murphy SM. Bogdanova-Mihaylova P, et al. Among authors: alexander md. Eur J Neurol. 2018 Feb;25(2):e22-e23. doi: 10.1111/ene.13532. Eur J Neurol. 2018. PMID: 29356258 No abstract available.

6

Bogdanova-Mihaylova P, Austin N, Alexander MD, Cassidy L, Early A, Murphy RP, Murphy SM, Walsh RA. Bogdanova-Mihaylova P, et al. Among authors: alexander md. Mov Disord Clin Pract. 2016 Jul 18;4(2):258-262. doi: 10.1002/mdc3.12396. eCollection 2017 Mar-Apr. Mov Disord Clin Pract. 2016. PMID: 30838263 Free PMC article.

7

Clinical spectrum of AIFM1-associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindness.

Bogdanova-Mihaylova P, Alexander MD, Murphy RP, Chen H, Healy DG, Walsh RA, Murphy SM. Bogdanova-Mihaylova P, et al. Among authors: alexander md. J Peripher Nerv Syst. 2019 Dec;24(4):348-353. doi: 10.1111/jns.12348. Epub 2019 Oct 10. J Peripher Nerv Syst. 2019. PMID: 31523922

8

Spastic ataxia associated with colour vision deficiency due to DDHD2 mutations.

Bogdanova-Mihaylova P, Austin N, Alexander MD, Cassidy L, Murphy RP, Walsh RA, Murphy SM. Bogdanova-Mihaylova P, et al. Among authors: alexander md. Eur J Neurol. 2020 Jan;27(1):e9-e10. doi: 10.1111/ene.14075. Epub 2019 Sep 18. Eur J Neurol. 2020. PMID: 31532039 No abstract available.

9

Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1.

O'Donnell L, Blakely EL, Baty K, Alexander M, Bogdanova-Mihaylova P, Craig J, Walsh R, Brett F, Taylor RW, Murphy SM. O'Donnell L, et al. J Neuromuscul Dis. 2020;7(3):355-360. doi: 10.3233/JND-200486. J Neuromuscul Dis. 2020. PMID: 32310184

10

Hypoglossal palsy from an atlanto-axial synovial cyst.

Vaughan D, Murphy SM, Alexander MD, Walsh RA. Vaughan D, et al. Among authors: alexander md. Pract Neurol. 2020 Oct;20(5):427-428. doi: 10.1136/practneurol-2020-002504. Epub 2020 May 4. Pract Neurol. 2020. PMID: 32366594 No abstract available.

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