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Results by year

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

Year Number of Results
1965 1
1968 1
1969 1
1970 1
1973 2
1976 1
1978 1
1981 2
1983 2
1984 3
1985 1
1986 1
1987 1
1988 3
1989 1
1990 2
1991 4
1993 1
1995 3
1996 3
1997 3
1998 1
1999 1
2000 1
2001 1
2002 4
2003 1
2004 2
2005 3
2006 1
2007 2
2008 1
2009 3
2010 3
2011 4
2012 2
2013 6
2014 6
2015 1
2016 2
2017 4
2018 4
2019 2
2021 2
2022 1
2024 0

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Search Results

89 results

Results by year

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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.
Echinococcosis.
Taratuto AL, Venturiello SM. Taratuto AL, et al. Brain Pathol. 1997 Jan;7(1):673-9. doi: 10.1111/j.1750-3639.1997.tb01082.x. Brain Pathol. 1997. PMID: 9034573 Free PMC article. Review.
Trichinosis.
Taratuto AL, Venturiello SM. Taratuto AL, et al. Brain Pathol. 1997 Jan;7(1):663-72. doi: 10.1111/j.1750-3639.1997.tb01081.x. Brain Pathol. 1997. PMID: 9034572 Free PMC article.
[Argentine consensus on late-onset Pompe's disease].
Dubrovsky A, Fulgenzi E, De Vito EL, Barroso F, Berardo A, Bettini M, Binaghi D, Calabrese E, Carlés D, Chaves M, Chloca F, Conti E, Corderi J, Di Gennaro F, Ferradás N, Jáuregui A, Lubieniecki F, Mazia C, Medina M, Pirra L, Politei J, Reisin R, Rosa AL, Rugiero M, Salutto V, Schenone A, Sussini M, Taratuto AL. Dubrovsky A, et al. Among authors: taratuto al. Medicina (B Aires). 2018;78 Suppl 1:1-23. Medicina (B Aires). 2018. PMID: 30179846 Free article. Spanish.
Muscle MRI in pediatrics: clinical, pathological and genetic correlation.
Cejas CP, Serra MM, Galvez DFG, Cavassa EA, Taratuto AL, Vazquez GA, Massaro MEL, Schteinschneider AV. Cejas CP, et al. Among authors: taratuto al. Pediatr Radiol. 2017 May;47(6):724-735. doi: 10.1007/s00247-016-3777-6. Epub 2017 Jan 19. Pediatr Radiol. 2017. PMID: 28102454 Review.
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.
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.
Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010.
Alcalde-Cabero E, Almazan-Isla J, Brandel JP, Breithaupt M, Catarino J, Collins S, Hayback J, Hoftberger R, Kahana E, Kovacs GG, Ladogana A, Mitrova E, Molesworth A, Nakamura Y, Pocchiari M, Popovic M, Ruiz-Tovar M, Taratuto A, van Duijn C, Yamada M, Will RG, Zerr I, de Pedro Cuesta J. Alcalde-Cabero E, et al. Among authors: taratuto a. Euro Surveill. 2012 Apr 12;17(15):20144. Euro Surveill. 2012. PMID: 22516047 Free article. Review.
89 results