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93 results

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Page 1
Movement-related cortical potentials.
Hallett M. Hallett M. Electromyogr Clin Neurophysiol. 1994 Jan-Feb;34(1):5-13. Electromyogr Clin Neurophysiol. 1994. PMID: 8168458 Review.
The fpMP appears to represent feedback from the movement and may originate, in part, from the supplementary motor area. In patients with congenital mirror movements, the isMP occurs bilaterally. In patients with Parkinson's disease and cerebellar disease, the …
The fpMP appears to represent feedback from the movement and may originate, in part, from the supplementary motor area. In patients with …
Noncanonical Roles of RAD51.
Thomas M, Dubacq C, Rabut E, Lopez BS, Guirouilh-Barbat J. Thomas M, et al. Cells. 2023 Apr 15;12(8):1169. doi: 10.3390/cells12081169. Cells. 2023. PMID: 37190078 Free PMC article. Review.
Finally, RAD51 pathogenic variants have been described in the congenital mirror movement syndrome, revealing an unexpected role in brain development. In this review, we present and discuss the different noncanonical roles of RAD51, whose presence does not aut …
Finally, RAD51 pathogenic variants have been described in the congenital mirror movement syndrome, revealing an unexpec …
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Marsh APL, Edwards TJ, Galea C, Cooper HM, Engle EC, Jamuar SS, Méneret A, Moutard ML, Nava C, Rastetter A, Robinson G, Rouleau G, Roze E, Spencer-Smith M, Trouillard O, Billette de Villemeur T, Walsh CA, Yu TW; IRC5 Consortium; Heron D, Sherr EH, Richards LJ, Depienne C, Leventer RJ, Lockhart PJ. Marsh APL, et al. Hum Mutat. 2018 Jan;39(1):23-39. doi: 10.1002/humu.23361. Epub 2017 Nov 11. Hum Mutat. 2018. PMID: 29068161 Free PMC article. Review.
Monoallelic, missense, and predicted loss-of-function DCC mutations cause congenital mirror movements, isolated agenesis of the corpus callosum (ACC), or both. Biallelic, predicted loss-of-function DCC mutations cause developmental split brain syndrome (DSBS) …
Monoallelic, missense, and predicted loss-of-function DCC mutations cause congenital mirror movements, isolated agenesi …
Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.
Franz EA, Chiaroni-Clarke R, Woodrow S, Glendining KA, Jasoni CL, Robertson SP, Gardner RJM, Markie D. Franz EA, et al. J Neurol Sci. 2015 Apr 15;351(1-2):140-145. doi: 10.1016/j.jns.2015.03.006. Epub 2015 Mar 10. J Neurol Sci. 2015. PMID: 25813273
Congenital mirror movements (CMM) is a disorder characterized by unintentional mirroring in homologous motor systems of voluntary movements on the opposite side, usually affecting the distal upper extremities. ...
Congenital mirror movements (CMM) is a disorder characterized by unintentional mirroring in homologous motor systems of
Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes.
Knight JL, Barker MS, Edwards TJ, Barnby JM, Richards LJ, Robinson GA. Knight JL, et al. Cortex. 2023 Apr;161:38-50. doi: 10.1016/j.cortex.2023.01.008. Epub 2023 Feb 19. Cortex. 2023. PMID: 36889039 Free article.
One specific finding in some individuals with corpus callosum dysgenesis is "congenital mirror movement disorder", which is the presence of involuntary movements on one side of the body that mimic voluntary movements of the other side. ...
One specific finding in some individuals with corpus callosum dysgenesis is "congenital mirror movement disorder", whic …
Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.
Demirayak P, Onat OE, Gevrekci AÖ, Gülsüner S, Uysal H, Bilgen RS, Doerschner K, Özçelik TS, Boyacı H. Demirayak P, et al. Diagn Interv Radiol. 2018 Nov;24(6):392-401. doi: 10.5152/dir.2018.18096. Diagn Interv Radiol. 2018. PMID: 30406765 Free PMC article.
PURPOSE: Congenital mirror movement disorder (CMMD) is characterized by unintended, nonsuppressible, homologous mirroring activity contralateral to the movement on the intended side of the body. ...
PURPOSE: Congenital mirror movement disorder (CMMD) is characterized by unintended, nonsuppressible, homologous mirrori …
Novel DCC variants in congenital mirror movements and evaluation of disease-associated missense variants.
Bierhals T, Korenke GC, Baethmann M, Marín LL, Staudt M, Kutsche K. Bierhals T, et al. Eur J Med Genet. 2018 Jun;61(6):329-334. doi: 10.1016/j.ejmg.2018.01.010. Epub 2018 May 7. Eur J Med Genet. 2018. PMID: 29366874
Congenital mirror movements (CMM) are involuntary movements of one side of the body that mirror intentional movements of the other side. ...
Congenital mirror movements (CMM) are involuntary movements of one side of the body that mirror intentional movements o
93 results