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Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.
Olivé M, Odgerel Z, Martínez A, Poza JJ, Bragado FG, Zabalza RJ, Jericó I, Gonzalez-Mera L, Shatunov A, Lee HS, Armstrong J, Maraví E, Arroyo MR, Pascual-Calvet J, Navarro C, Paradas C, Huerta M, Marquez F, Rivas EG, Pou A, Ferrer I, Goldfarb LG. Olivé M, et al. Among authors: armstrong j. Neuromuscul Disord. 2011 Aug;21(8):533-42. doi: 10.1016/j.nmd.2011.05.002. Epub 2011 Jun 14. Neuromuscul Disord. 2011. PMID: 21676617 Free PMC article.
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.
Olivé M, Armstrong J, Miralles F, Pou A, Fardeau M, Gonzalez L, Martínez F, Fischer D, Martínez Matos JA, Shatunov A, Goldfarb L, Ferrer I. Olivé M, et al. Among authors: armstrong j. Neuromuscul Disord. 2007 Jun;17(6):443-50. doi: 10.1016/j.nmd.2007.02.009. Epub 2007 Apr 5. Neuromuscul Disord. 2007. PMID: 17418574 Free PMC article.
Spinocerebellar ataxia type 2 (SCA2) with white matter involvement.
Armstrong J, Bonaventura I, Rojo A, González G, Corral J, Nadal N, Volpini V, Ferrer I. Armstrong J, et al. Neurosci Lett. 2005 Jun 24;381(3):247-51. doi: 10.1016/j.neulet.2005.02.063. Epub 2005 Mar 17. Neurosci Lett. 2005. PMID: 15896478
Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study.
Ferrer I, Armstrong J, Capellari S, Parchi P, Arzberger T, Bell J, Budka H, Ströbel T, Giaccone G, Rossi G, Bogdanovic N, Fakai P, Schmitt A, Riederers P, Al-Sarraj S, Ravid R, Kretzschmar H. Ferrer I, et al. Among authors: armstrong j. Brain Pathol. 2007 Jul;17(3):297-303. doi: 10.1111/j.1750-3639.2007.00073.x. Epub 2007 Apr 23. Brain Pathol. 2007. PMID: 17465988 Free PMC article.
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA.
Revencu N, Eijkelenboom A, Bracquemart C, Alhopuro P, Armstrong J, Baselga E, Cesario C, Dentici ML, Eyries M, Frisk S, Karstensen HG, Gene-Olaciregui N, Kivirikko S, Lavarino C, Mero IL, Michiels R, Pisaneschi E, Schönewolf-Greulich B, Wieland I, Zenker M, Vikkula M. Revencu N, et al. Among authors: armstrong j. Orphanet J Rare Dis. 2024 May 22;19(1):213. doi: 10.1186/s13023-024-03196-9. Orphanet J Rare Dis. 2024. PMID: 38778413 Free PMC article.
Multi-omics in MECP2 duplication syndrome patients and carriers.
Pascual-Alonso A, Xiol C, Smirnov D, Kopajtich R, Prokisch H, Armstrong J. Pascual-Alonso A, et al. Among authors: armstrong j. Eur J Neurosci. 2024 May 15. doi: 10.1111/ejn.16389. Online ahead of print. Eur J Neurosci. 2024. PMID: 38746988
2,569 results