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96 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 …
Congenital mirror movements.
Schott GD, Wyke MA. Schott GD, et al. J Neurol Neurosurg Psychiatry. 1981 Jul;44(7):586-99. doi: 10.1136/jnnp.44.7.586. J Neurol Neurosurg Psychiatry. 1981. PMID: 7288446 Free PMC article.
In this report are described seven patients assessed clinically and neuropsychologically in whom mirror movements affecting predominantly the hands occurred as a congenital disorder. These mirror movements, representing a specific type of abnormal synkinesia, …
In this report are described seven patients assessed clinically and neuropsychologically in whom mirror movements affecting predominantly th …
A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC.
Chaudhari K, Zhang K, Yam PT, Zang Y, Kramer DA, Gagnon S, Schlienger S, Calabretta S, Michaud JF, Collins M, Wang J, Srour M, Chen B, Charron F, Bashaw GJ. Chaudhari K, et al. Sci Signal. 2024 Oct;17(856):eadk2345. doi: 10.1126/scisignal.adk2345. Epub 2024 Oct 1. Sci Signal. 2024. PMID: 39353037 Free PMC article.
Variants in DCC are frequently associated with congenital mirror movements (CMMs). A CMM-associated variant in the cytoplasmic tail of DCC is located in a conserved motif predicted to bind to a regulator of actin dynamics called the WAVE (Wiskott-Aldrich synd …
Variants in DCC are frequently associated with congenital mirror movements (CMMs). A CMM-associated variant in the cyto …
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.
Collins Hutchinson ML, St-Onge J, Schlienger S, Boudrahem-Addour N, Mougharbel L, Michaud JF, Lloyd C, Bruneau E, Roux C, Sahly AN, Osterman B, Myers KA, Rouleau GA, Jimenez Cruz DA, Rivière JB, Accogli A, Charron F, Srour M. Collins Hutchinson ML, et al. Mov Disord. 2024 Feb;39(2):400-410. doi: 10.1002/mds.29669. Epub 2024 Feb 5. Mov Disord. 2024. PMID: 38314870
BACKGROUND: Congenital mirror movements (CMM) is a rare neurodevelopmental disorder characterized by involuntary movements from one side of the body that mirror voluntary movements on the opposite side. ...
BACKGROUND: Congenital mirror movements (CMM) is a rare neurodevelopmental disorder characterized by involuntary moveme …
Human disorders of axon guidance.
Nugent AA, Kolpak AL, Engle EC. Nugent AA, et al. Curr Opin Neurobiol. 2012 Oct;22(5):837-43. doi: 10.1016/j.conb.2012.02.006. Epub 2012 Mar 5. Curr Opin Neurobiol. 2012. PMID: 22398400 Free PMC article. Review.
In this review, we summarize the recent clinical, genetic and molecular advances with regard to three human disorders of axon guidance: Horizontal gaze palsy with progressive scoliosis, Congenital mirror movements, and Congenital fibrosis of the extrao …
In this review, we summarize the recent clinical, genetic and molecular advances with regard to three human disorders of axon guidance: Hori …
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 …
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 …
96 results