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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2017 | 3 |
2022 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
Central core myopathy with autophagy.
Muscle Nerve. 2017 Aug;56(2):E8-E9. doi: 10.1002/mus.25594. Epub 2017 Mar 21.
Muscle Nerve. 2017.
PMID: 28164363
No abstract available.
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms.
Cotta A, Souza LS, Carvalho E, Feitosa LN, Cunha A Jr, Navarro MM, Valicek J, Menezes MM, Neves SVN, Xavier-Neto R, Vargas AP, Takata RI, Paim JF, Vainzof M.
Cotta A, et al. Among authors: xavier neto r.
Genes (Basel). 2022 Apr 26;13(5):760. doi: 10.3390/genes13050760.
Genes (Basel). 2022.
PMID: 35627144
Free PMC article.
Item in Clipboard
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Cotta A, Carvalho E, da-Cunha-Júnior AL, Paim JF, Navarro MM, Valicek J, Menezes MM, Nunes SV, Xavier Neto R, Takata RI, Vargas AP.
Cotta A, et al. Among authors: xavier neto r.
Arq Neuropsiquiatr. 2014 Sep;72(9):721-34. doi: 10.1590/0004-282x20140110.
Arq Neuropsiquiatr. 2014.
PMID: 25252238
Free article.
Review.
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Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers.
Cotta A, Paim JF, Carvalho E, Navarro MM, Valicek J, da-Cunha-Junior AL, Menezes MM, Nunes SV, Xavier-Neto R, da Silveira EB, Costa-E-Silva C, Takata RI, Vargas AP.
Cotta A, et al. Among authors: xavier neto r.
Can J Neurol Sci. 2017 May;44(3):304-310. doi: 10.1017/cjn.2016.448. Epub 2017 Feb 9.
Can J Neurol Sci. 2017.
PMID: 28181471
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The relative frequency of common neuromuscular diagnoses in a reference center.
Cotta A, Paim JF, Carvalho E, da-Cunha-Júnior AL, Navarro MM, Valicek J, Menezes MM, Nunes SV, Xavier-Neto R, Baptista S Junior, Lima LR, Takata RI, Vargas AP.
Cotta A, et al. Among authors: xavier neto r.
Arq Neuropsiquiatr. 2017 Nov;75(11):789-795. doi: 10.1590/0004-282X20170151.
Arq Neuropsiquiatr. 2017.
PMID: 29236822
Free article.
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Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern.
Cotta A, Paim JF, da-Cunha-Junior AL, Neto RX, Nunes SV, Navarro MM, Valicek J, Carvalho E, Yamamoto LU, Almeida CF, Braz SV, Takata RI, Vainzof M.
Cotta A, et al. Among authors: neto rx.
BMC Clin Pathol. 2014 Oct 4;14:41. doi: 10.1186/1472-6890-14-41. eCollection 2014.
BMC Clin Pathol. 2014.
PMID: 25298746
Free PMC article.
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