Publications by authors named "Violeta Mihaylova"

20 Publications

  • Page 1 of 1

Evoked Potentials in Patients With Wilson Disease.

J Clin Neurophysiol 2020 Nov 10. Epub 2020 Nov 10.

Department of Neurology, University Hospital "Alexandrovska," Medical University Sofia, Sofia, Bulgaria.

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November 2020

Novel truncating mutations of causing congenital myopathy in a Swiss patient.

Neurol Genet 2020 Aug 9;6(4):e458. Epub 2020 Jun 9.

Department of Neurology (V.M., H.H.J.), University Hospital and University of Zurich; and Genetica (F.C., Y.H., R.S.), Human Genetics and Genetic Counselling Unit, Zurich, Switzerland.

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August 2020

Satellite cell content in Huntington's disease patients in response to endurance training.

Orphanet J Rare Dis 2019 06 11;14(1):135. Epub 2019 Jun 11.

Research and Performance Center for Elite Athleticism, OYM, Lorzenparkstrasse 12, 6330, Cham, Switzerland.

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June 2019

Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients.

Orphanet J Rare Dis 2017 12 19;12(1):184. Epub 2017 Dec 19.

Department of Neurology, University Hospital Zurich, , University of Zurich, Frauenklinikstrasse 26, 8091, Zurich, Switzerland.

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December 2017

Muskelkrämpfe – die neurologische Perspektive.

Praxis (Bern 1994) 2017;106(25):1391-1396

1 Klinik für Neurologie, Universitätsspital Zürich.

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January 2017

Exercise effects in Huntington disease.

J Neurol 2017 Jan 17;264(1):32-39. Epub 2016 Oct 17.

Department of Neurology, University Hospital and University of Zurich, Frauenklinikstrasse 26, 8091, Zurich, Switzerland.

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January 2017

GNE myopathy in Roma patients homozygous for the p.I618T founder mutation.

Neuromuscul Disord 2015 Sep 13;25(9):713-8. Epub 2015 Jul 13.

Department of Neurology, University Hospital Alexandrovska, Sofia Medical University, Sofia, Bulgaria; Department of Cognitive Science and Psychology, New Bulgarian University, Sofia, Bulgaria.

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September 2015

Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.

Epilepsia 2009 Jul 23;50(7):1679-88. Epub 2009 Mar 23.

Laboratory for Molecular Genetics, Centre for Medical Research and Western Australian Institute for Medical Research, The University of Western Australia, Perth, Australia.

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July 2009

Congenital myasthenic syndromes: spotlight on genetic defects of neuromuscular transmission.

Expert Rev Mol Med 2007 Aug 9;9(22):1-20. Epub 2007 Aug 9.

Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University, Munich, Germany.

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August 2007