Katsiaryna Belaya

Katsiaryna Belaya

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Katsiaryna Belaya

Katsiaryna Belaya

Publications by authors named "Katsiaryna Belaya"

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16Publications

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Late presentations of congenital myasthenic syndromes: How many do we miss?

Muscle Nerve 2016 10 9;54(4):721-7. Epub 2016 Jul 9.

Neuroimmunology Clinic, Concord Hospital and University of Sydney, NSW, Australia.

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http://dx.doi.org/10.1002/mus.25085DOI Listing
October 2016

Clinical features of the myasthenic syndrome arising from mutations in GMPPB.

J Neurol Neurosurg Psychiatry 2016 08 4;87(8):802-9. Epub 2016 May 4.

Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1136/jnnp-2016-313163DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047737PMC
August 2016

Collagen Q--a potential target for autoantibodies in myasthenia gravis.

J Neurol Sci 2015 Jan 18;348(1-2):241-4. Epub 2014 Dec 18.

Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Weatherall Institute of Molecular Medicine, Neurosciences Group, OX3 9DS, Oxford, UK. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2014.12.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044427PMC
January 2015

Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.

J Neurol Neurosurg Psychiatry 2013 Oct 27;84(10):1119-25. Epub 2013 Feb 27.

Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.

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http://jnnp.bmj.com/content/84/10/1119.full.pdf
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http://jnnp.bmj.com/cgi/doi/10.1136/jnnp-2012-304716
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http://dx.doi.org/10.1136/jnnp-2012-304716DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044426PMC
October 2013

Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1.

Neuromuscul Disord 2013 Jun 13;23(6):469-72. Epub 2013 Apr 13.

Neurology Department, Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1016/j.nmd.2013.03.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746154PMC
June 2013

Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome.

Ann N Y Acad Sci 2012 Dec;1275:29-35

Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1111/j.1749-6632.2012.06790.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044425PMC
December 2012

The search for new antigenic targets in myasthenia gravis.

Ann N Y Acad Sci 2012 Dec;1275:123-8

Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom.

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http://dx.doi.org/10.1111/j.1749-6632.2012.06833.xDOI Listing
December 2012

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.

Hum Mol Genet 2012 Sep 1;21(17):3765-75. Epub 2012 Jun 1.

Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.

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http://dx.doi.org/10.1093/hmg/dds198DOI Listing
September 2012

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

Am J Hum Genet 2012 Jul 27;91(1):193-201. Epub 2012 Jun 27.

Neurosciences Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, University of Oxford, UK.

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http://dx.doi.org/10.1016/j.ajhg.2012.05.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397259PMC
July 2012

Using the mRNA-MS2/MS2CP-FP system to study mRNA transport during Drosophila oogenesis.

Methods Mol Biol 2011 ;714:265-83

The Gurdon Institute, University of Cambridge, Cambridge, UK.

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http://dx.doi.org/10.1007/978-1-61779-005-8_17DOI Listing
July 2011

In vivo imaging of oskar mRNA transport reveals the mechanism of posterior localization.

Cell 2008 Sep;134(5):843-53

The Gurdon Institute and the Department of Genetics, University of Cambridge, Tennis Court Road, CB2 1QN Cambridge, UK.

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http://dx.doi.org/10.1016/j.cell.2008.06.053DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585615PMC
September 2008

FLIPing heterokaryons to analyze nucleo-cytoplasmic shuttling of yeast proteins.

RNA 2006 May 15;12(5):921-30. Epub 2006 Mar 15.

Wellcome Trust Centre for Cell Biology, University of Edinburgh, United Kingdom.

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http://www.rnajournal.org/cgi/doi/10.1261/rna.2301806
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http://dx.doi.org/10.1261/rna.2301806DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1440899PMC
May 2006