Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2014 | 2 |
2017 | 2 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms.
Genes (Basel). 2022 Apr 26;13(5):760. doi: 10.3390/genes13050760.
Genes (Basel). 2022.
PMID: 35627144
Free PMC article.
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: takata ri.
Arq Neuropsiquiatr. 2014 Sep;72(9):721-34. doi: 10.1590/0004-282x20140110.
Arq Neuropsiquiatr. 2014.
PMID: 25252238
Free article.
Review.
Item in Clipboard
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: takata ri.
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
Item in Clipboard
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: takata ri.
Arq Neuropsiquiatr. 2017 Nov;75(11):789-795. doi: 10.1590/0004-282X20170151.
Arq Neuropsiquiatr. 2017.
PMID: 29236822
Free article.
Item in Clipboard
Muscle fat replacement and modified ragged red fibers in two patients with reversible infantile respiratory chain deficiency.
Cotta A, Carvalho E, da-Cunha-Junior A, Navarro MM, Paim JF, Valicek J, Baptista-Junior S, da Silveira EB, Lima MI, Carellos EVM, de-La-Rocque-Ferreira A, Takata RI, Horvath R.
Cotta A, et al. Among authors: takata ri.
Neuromuscul Disord. 2021 Jun;31(6):551-557. doi: 10.1016/j.nmd.2021.02.017. Epub 2021 Feb 21.
Neuromuscul Disord. 2021.
PMID: 33832841
Item in Clipboard
Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes.
Carvalho DR, Brand GD, Brum JM, Takata RI, Speck-Martins CE, Pratesi R.
Carvalho DR, et al. Among authors: takata ri.
Gene. 2012 Nov 1;509(1):124-30. doi: 10.1016/j.gene.2012.08.003. Epub 2012 Aug 16.
Gene. 2012.
PMID: 22959135
Item in Clipboard
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: takata ri.
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.
Item in Clipboard
Cite
Cite