Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Priya Shanmugarajah"'
Autor:
Channa Hewamadduma, James Lilleker, Phillip Kelly, Isobel White, Douglas Whiter, Mahjabin Islam, Paul Campbell, Sadaf Mehboob, Frederick Vonberg, Priya Shanmugarajah, Helen Grote, Stuart Viegas, Christopher Turner
Publikováno v:
Monday, April 24.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9f3c06c3e8ffdd84c5b685123b64e8e
https://doi.org/10.1212/wnl.0000000000203882
https://doi.org/10.1212/wnl.0000000000203882
Autor:
Pamela J. Shaw, John P Franklin, James J.P. Alix, David Paling, Johnathan Cooper-Knock, Priya Shanmugarajah, Tobias Moll, Marios Hadjivissiliou, Nicholas J. Beauchamp, Christopher J McDermott, Michael Pattrick, Helia Ghahremani Nezhad, Thomas M Jenkins
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 22:579-582
Spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS) share a common molecular basis: both are associated with CAG-repeat expansion of ATXN2 and TDP-43-positive neuronal cytoplasmic inclusions. To date, the two disorders are vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce9af001d63f4808a5d3003ddb5e3213
https://doi.org/10.1080/21678421.2020.1853172
https://doi.org/10.1080/21678421.2020.1853172
Autor:
Fu Chuen Kon, Mohammed Akil, Rachael Kilding, Kar-Ping Kuet, Priya Shanmugarajah, Nigel Hoggard, Marios Hadjivassiliou
Publikováno v:
Rheumatology. 61
Background/Aims Cerebellar ataxia is an uncommon neurological complication of Primary Sjogren’s Syndrome (PSS), with case reports being the highest level of evidence available. The underlying disease pathogenesis is unknown, although an immunologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beca47f7bea622efd9063bd3f58bbfa9
https://doi.org/10.1093/rheumatology/keac133.234
https://doi.org/10.1093/rheumatology/keac133.234
Autor:
Jon M Dickson, Alice Brockington, Priya Shanmugarajah, Markus Reuber, Gary Dennis, Philippa Davies, Stephen Howell, Theocharis Tsironis, Richard A. Grünewald
Publikováno v:
Seizure. 79:8-13
Purpose On 24/04/2018, the United Kingdom (UK) Medicines and Healthcare Products Regulatory Agency (MHRA) clarified previous policies by issuing a statement, that the use of sodium valproate is contraindicated in women of childbearing potential unles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d26c5d2d4cb4fb1eb3b7f59c7599cbd
https://doi.org/10.1016/j.seizure.2020.03.015
https://doi.org/10.1016/j.seizure.2020.03.015
Publikováno v:
Cerebellum (London, England)
Superficial siderosis describes haemosiderin deposition on the surface of the brain. When present on infratentorial structures, it can cause ataxia, sensorineural hearing loss and pyramidal signs. There is no proven treatment and patients experience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::091537d01f76cecfa0651f75bb21c36a
Autor:
Mohit Litesh, Paul R Campbell, Sadaf Mehboob, Frederick Vonberg, Woon Senn Koh, Phillip Kelly, Priya Shanmugarajah, Stuart Viegas, James B Lilleker, Channa Hewamadduma
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:e2.186
Myotonic Dystrophy Type 1 (DM1) is the most common muscular dystrophy in adults. Structured multi- disciplinary care is required to manage the multi-system involvement, to improve patient safety, and to reduce mortality and morbidity. Previous audits
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a1b611c7affbb48f9b9d90956bb1fbe
https://doi.org/10.1136/jnnp-2022-abn2.4
https://doi.org/10.1136/jnnp-2022-abn2.4
Autor:
Helia, Ghahremani Nezhad, John P, Franklin, James J P, Alix, Tobias, Moll, Michael, Pattrick, Johnathan, Cooper-Knock, Priya, Shanmugarajah, Nick J, Beauchamp, Marios, Hadjivissiliou, David, Paling, Christopher, Mcdermott, Pamela J, Shaw, Thomas M, Jenkins
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 22(7-8)
Spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS) share a common molecular basis: both are associated with CAG-repeat expansion of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87af84365d3c3c134edb91c04231f2c5
https://pubmed.ncbi.nlm.nih.gov/33284045
https://pubmed.ncbi.nlm.nih.gov/33284045
Autor:
Nigel Hoggard, Richard A. Grünewald, Priya Shanmugarajah, David S Sanders, Marios Hadjivassiliou
Publikováno v:
Neurology. 89:705-709
Objective:To evaluate the effect of gluten free diet (GFD) on magnetic resonance spectroscopy (MRS) of the cerebellum in patients with gluten ataxia (GA).Methods:Patients with GA, defined as sporadic ataxia with positive antigliadin antibodies in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::094c7fa54b4a2dab85e70268574c5661
https://doi.org/10.1212/wnl.0000000000004237
https://doi.org/10.1212/wnl.0000000000004237
Autor:
S Duty, R Warburton, K Garrard, Juliet M. Taylor, Ptolemaios G. Sarrigiannis, Marios Hadjivassiliou, Richard A. Grünewald, Nicholas J. Beauchamp, Nigel Hoggard, D Friend, Joanne Martindale, Priya Shanmugarajah, David S Sanders
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 88:301-309
Background Cerebellar ataxias are the result of diverse disease processes that can be genetic or acquired. Establishing a diagnosis requires a methodical approach with expert clinical evaluation and investigations. We describe the causes of ataxia in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc5a59c51db4c1a003f8ca1460f8219b
https://doi.org/10.1136/jnnp-2016-314863
https://doi.org/10.1136/jnnp-2016-314863
Autor:
James J P, Alix, Taimour, Alam, Kate, Garrard, Joanne, Martindale, Priya, Shanmugarajah, D, Ganesh Rao, Marios, Hadjivassiliou
Publikováno v:
Musclenerve. 55(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc0318375fc013f0c74017aaccf87211
https://pubmed.ncbi.nlm.nih.gov/27491039
https://pubmed.ncbi.nlm.nih.gov/27491039