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Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study.
Schiava M, Ikenaga C, Villar-Quiles RN, Caballero-Ávila M, Topf A, Nishino I, Kimonis V, Udd B, Schoser B, Zanoteli E, Souza PVS, Tasca G, Lloyd T, Lopez-de Munain A, Paradas C, Pegoraro E, Nadaj-Pakleza A, De Bleecker J, Badrising U, Alonso-Jiménez A, Kostera-Pruszczyk A, Miralles F, Shin JH, Bevilacqua JA, Olivé M, Vorgerd M, Kley R, Brady S, Williams T, Domínguez-González C, Papadimas GK, Warman-Chardon J, Claeys KG, de Visser M, Muelas N, LaForet P, Malfatti E, Alfano LN, Nair SS, Manousakis G, Kushlaf HA, Harms MB, Nance C, Ramos-Fransi A, Rodolico C, Hewamadduma C, Cetin H, García-García J, Pál E, Farrugia ME, Lamont PJ, Quinn C, Nedkova-Hristova V, Peric S, Luo S, Oldfors A, Taylor K, Ralston S, Stojkovic T, Weihl C, Diaz-Manera J; VCP International Study Group; VCP International Study Group. Schiava M, et al. Among authors: nair ss. J Neurol Neurosurg Psychiatry. 2022 Jul 27:jnnp-2022-328921. doi: 10.1136/jnnp-2022-328921. Online ahead of print. J Neurol Neurosurg Psychiatry. 2022. PMID: 35896379 Free PMC article.
Clinical Spectrum of Biopsy Proven Mitochondrial Myopathy.
Menon D, Nair SS, Radhakrishnan N, Saraf UU, Nair M. Menon D, et al. Among authors: nair m, nair ss. Neurol India. 2023 Nov-Dec;71(6):1192-1196. doi: 10.4103/0028-3886.391399. Neurol India. 2023. PMID: 38174457 Free article.
Brown's syndrome: a rare cause of vertical diplopia.
Manisha KY, Nair SS, Kumar AA, Sundaram S. Manisha KY, et al. Among authors: nair ss. Pract Neurol. 2024 Apr 8:pn-2023-004028. doi: 10.1136/pn-2023-004028. Online ahead of print. Pract Neurol. 2024. PMID: 38589214 No abstract available.
382 results