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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Renaud M, Moreira MC, Ben Monga B, Rodriguez D, Debs R, Charles P, Chaouch M, Ferrat F, Laurencin C, Vercueil L, Mallaret M, M'Zahem A, Pacha LA, Tazir M, Tilikete C, Ollagnon E, Ochsner F, Kuntzer T, Jung HH, Beis JM, Netter JC, Djamshidian A, Bower M, Bottani A, Walsh R, Murphy S, Reiley T, Bieth É, Roelens F, Poll-The BT, Lourenço CM, Jardim LB, Straussberg R, Landrieu P, Roze E, Thobois S, Pouget J, Guissart C, Goizet C, Dürr A, Tranchant C, Koenig M, Anheim M. Renaud M, et al. Among authors: murphy s. JAMA Neurol. 2018 Apr 1;75(4):495-502. doi: 10.1001/jamaneurol.2017.4373. JAMA Neurol. 2018. PMID: 29356829 Free PMC article.
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: murphy sm, murphy rp. 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.
Hypoglossal palsy from an atlanto-axial synovial cyst.
Vaughan D, Murphy SM, Alexander MD, Walsh RA. Vaughan D, et al. 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.
5,926 results