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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2004 2
2006 1
2007 1
2008 1
2009 2
2010 1
2011 1
2012 1
2013 5
2014 6
2015 1
2016 2
2017 2
2018 3
2019 2
2021 1
2022 1
2024 0

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31 results

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Page 1
'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies.
Garibaldi M, Rendu J, Brocard J, Lacene E, Fauré J, Brochier G, Beuvin M, Labasse C, Madelaine A, Malfatti E, Bevilacqua JA, Lubieniecki F, Monges S, Taratuto AL, Laporte J, Marty I, Antonini G, Romero NB. Garibaldi M, et al. Among authors: taratuto al. Acta Neuropathol Commun. 2019 Jan 5;7(1):3. doi: 10.1186/s40478-018-0655-5. Acta Neuropathol Commun. 2019. PMID: 30611313 Free PMC article.
Congenital myopathies and related disorders.
Taratuto AL. Taratuto AL. Curr Opin Neurol. 2002 Oct;15(5):553-61. doi: 10.1097/00019052-200210000-00006. Curr Opin Neurol. 2002. PMID: 12351999 Review.
[Dermatomyositis associated with anti-MDA5 autoantibody].
Collado MV, Gargiulo MLÁ, Gómez R, Gómez G, Pérez N, Suarez L, Taratuto AL, Aruj P. Collado MV, et al. Among authors: taratuto al. Medicina (B Aires). 2018;78(5):360-363. Medicina (B Aires). 2018. PMID: 30285929 Free article. Spanish.
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.
Schartner V, Romero NB, Donkervoort S, Treves S, Munot P, Pierson TM, Dabaj I, Malfatti E, Zaharieva IT, Zorzato F, Abath Neto O, Brochier G, Lornage X, Eymard B, Taratuto AL, Böhm J, Gonorazky H, Ramos-Platt L, Feng L, Phadke R, Bharucha-Goebel DX, Sumner CJ, Bui MT, Lacene E, Beuvin M, Labasse C, Dondaine N, Schneider R, Thompson J, Boland A, Deleuze JF, Matthews E, Pakleza AN, Sewry CA, Biancalana V, Quijano-Roy S, Muntoni F, Fardeau M, Bönnemann CG, Laporte J. Schartner V, et al. Among authors: taratuto al. Acta Neuropathol. 2017 Apr;133(4):517-533. doi: 10.1007/s00401-016-1656-8. Epub 2016 Dec 23. Acta Neuropathol. 2017. PMID: 28012042
CLN8 disease caused by large genomic deletions.
Beesley C, Guerreiro RJ, Bras JT, Williams RE, Taratuto AL, Eltze C, Mole SE. Beesley C, et al. Among authors: taratuto al. Mol Genet Genomic Med. 2016 Nov 23;5(1):85-91. doi: 10.1002/mgg3.263. eCollection 2017 Jan. Mol Genet Genomic Med. 2016. PMID: 28116333 Free PMC article.
Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.
Begué C, Martinetto H, Schultz M, Rojas E, Romero C, D'Giano C, Sevlever G, Somoza M, Taratuto AL. Begué C, et al. Among authors: taratuto al. Neuroepidemiology. 2011;37(3-4):193-202. doi: 10.1159/000331907. Epub 2011 Nov 5. Neuroepidemiology. 2011. PMID: 22067221
A 36-year-old man with headache and fever.
Riudavets MA, Lía Taratuto A, Pelorosso F, Sevlever G. Riudavets MA, et al. Among authors: lia taratuto a. Brain Pathol. 2018 Jul;28(4):581-582. doi: 10.1111/bpa.12622. Brain Pathol. 2018. PMID: 30133863 Free PMC article. No abstract available.
Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.
Labasse C, Brochier G, Taratuto AL, Cadot B, Rendu J, Monges S, Biancalana V, Quijano-Roy S, Bui MT, Chanut A, Madelaine A, Lacène E, Beuvin M, Amthor H, Servais L, de Feraudy Y, Erro M, Saccoliti M, Neto OA, Fauré J, Lannes B, Laugel V, Coppens S, Lubieniecki F, Bello AB, Laing N, Evangelista T, Laporte J, Böhm J, Romero NB. Labasse C, et al. Among authors: taratuto al. Acta Neuropathol Commun. 2022 Jul 9;10(1):101. doi: 10.1186/s40478-022-01400-0. Acta Neuropathol Commun. 2022. PMID: 35810298 Free PMC article.
Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies.
Ávila-Polo R, Malfatti E, Lornage X, Cheraud C, Nelson I, Nectoux J, Böhm J, Schneider R, Hedberg-Oldfors C, Eymard B, Monges S, Lubieniecki F, Brochier G, Thao Bui M, Madelaine A, Labasse C, Beuvin M, Lacène E, Boland A, Deleuze JF, Thompson J, Richard I, Taratuto AL, Udd B, Leturcq F, Bonne G, Oldfors A, Laporte J, Romero NB. Ávila-Polo R, et al. Among authors: taratuto al. J Neuropathol Exp Neurol. 2018 Dec 1;77(12):1101-1114. doi: 10.1093/jnen/nly095. J Neuropathol Exp Neurol. 2018. PMID: 30365001 Free article.
Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients.
Loos MA, Gomez G, Mayorga L, Caraballo RH, Eiroa HD, Obregon MG, Rugilo C, Lubieniecki F, Taratuto AL, Saccoliti M, Alonso CN, Aráoz HV. Loos MA, et al. Among authors: taratuto al. Mol Genet Metab Rep. 2021 Feb 25;27:100733. doi: 10.1016/j.ymgmr.2021.100733. eCollection 2021 Jun. Mol Genet Metab Rep. 2021. PMID: 33717984 Free PMC article.
31 results