Una-Marie Sheerin

Una-Marie Sheerin

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Una-Marie Sheerin

Una-Marie Sheerin

Publications by authors named "Una-Marie Sheerin"

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22Publications

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Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series.

J Neurol Neurosurg Psychiatry 2016 May 2;87(5):512-9. Epub 2015 May 2.

Department of Molecular Neuroscience, The National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, Queen Square, London, UK Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, Queen Square, London, UK.

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http://dx.doi.org/10.1136/jnnp-2015-310788DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853550PMC
May 2016

Exome Sequencing Identifies a Novel Homozygous Missense Mutation.

Mov Disord Clin Pract 2017 Jan-Feb;4(1):132-135. Epub 2016 Apr 26.

Parkinson's and Ageing Research Foundation Bangalore India.

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http://dx.doi.org/10.1002/mdc3.12353DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353396PMC
April 2016

The entity of parkinsonism and associated lipomatosis.

Neurology 2014 Oct 1;83(18):1673-4. Epub 2014 Oct 1.

From the UCL Institute of Neurology (M.S., U.-M.S., N.W., K.P.B.), London, UK; Attiko Hospital (M.S.), University of Athens, Greece; and Philipps University (M.S.), Marburg, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000000937DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223088PMC
October 2014

Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration.

Hum Mol Genet 2014 Sep 15;23(17):4621-38. Epub 2014 Apr 15.

Laboratory of Molecular Neurodegenerative Research Center for Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI 49503, USA

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http://dx.doi.org/10.1093/hmg/ddu178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119414PMC
September 2014

Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.

Mov Disord 2014 Aug 25;29(9):1108-16. Epub 2014 Jun 25.

Sobell Department of Motor Neuroscience and Movement Disorders, University College London, Institute of Neurology, London, United Kingdom.

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http://dx.doi.org/10.1002/mds.25933DOI Listing
August 2014

Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.

Mov Disord 2014 Jul 21;29(8):1060-4. Epub 2014 Apr 21.

Department of Clinical Neuroscience, Institute of Neurology, University College London, London, United Kingdom.

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http://dx.doi.org/10.1002/mds.25883DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190821PMC
July 2014

The phenotypic spectrum of DYT24 due to ANO3 mutations.

Mov Disord 2014 Jun 17;29(7):928-34. Epub 2014 Jan 17.

Sobell Department of Motor Neuroscience and Movement Disorders, University College London (UCL) Institute of Neurology, London, United Kingdom; Neurology Clinic, Attiko Hospital, University of Athens, Greece.

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http://doi.wiley.com/10.1002/mds.25802
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http://dx.doi.org/10.1002/mds.25802DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150528PMC
June 2014

Advances in the Genetics of Parkinson's Disease: A Guide for the Clinician.

Mov Disord Clin Pract 2014 Apr 10;1(1):3-13. Epub 2014 Apr 10.

UCL Department of Molecular Neuroscience and UCL Genetics Institute University College London London United Kingdom.

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http://dx.doi.org/10.1002/mdc3.12000DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6183020PMC
April 2014

ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.

Neurology 2014 Mar 21;82(12):1065-7. Epub 2014 Feb 21.

From the Department of Molecular Neuroscience (U.-M.S.) and Sobell Department of Motor Neuroscience and Movement Disorders (M.S., K.P.B.), UCL Institute of Neurology, London, UK; University of Kiel (S.A.S., G.D., F.H.), Movement Disorders Clinic, Germany; Department of Paediatrics (L.C.), Great Ormond Street Hospital, London, UK; Second Department of Neurology (M.S.), University of Athens, Greece; and UCL Department of Molecular Neuroscience and UCL Genetics Institute (N.W.W.), University College London, UK.

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http://dx.doi.org/10.1212/WNL.0000000000000254DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962990PMC
March 2014

Primary progressive multiple sclerosis developing in the context of young onset Parkinson's disease.

Mult Scler 2013 Jan 20;19(1):123-5. Epub 2012 Apr 20.

Charing Cross Hospital, London, UK.

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http://dx.doi.org/10.1177/1352458512445942DOI Listing
January 2013

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.

Neurosci Lett 2012 Jun 23;518(1):19-22. Epub 2012 Apr 23.

Department of Molecular Neuroscience and Reta Lila Weston Laboratories, Institute of Neurology, Queen Square House, Queen Square, London WC1N 3BG, United Kingdom.

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http://dx.doi.org/10.1016/j.neulet.2012.04.033DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769807PMC
June 2012

Screening for VPS35 mutations in Parkinson's disease.

Neurobiol Aging 2012 Apr 7;33(4):838.e1-5. Epub 2011 Dec 7.

Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.10.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629567PMC
April 2012