Elizabeth Wraige

Elizabeth Wraige

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Elizabeth Wraige

Elizabeth Wraige

Publications by authors named "Elizabeth Wraige"

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Seeking normality: Parents' experiences of childhood stroke.

Child Care Health Dev 2019 01 15;45(1):89-95. Epub 2018 Oct 15.

Paediatric Neuroscience, Evelina London Children's Hospital.

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http://dx.doi.org/10.1111/cch.12622DOI Listing
January 2019

Self-reported needs after pediatric stroke.

Eur J Paediatr Neurol 2018 Sep 18;22(5):791-796. Epub 2018 Jun 18.

King's College London, UK.

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https://linkinghub.elsevier.com/retrieve/pii/S10903798173194
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http://dx.doi.org/10.1016/j.ejpn.2018.06.003DOI Listing
September 2018

Neuroimaging in Juvenile Alexander Disease: Tumour-like Brainstem Lesions.

Ann Acad Med Singapore 2018 05;47(5):191-193

Department of Diagnostic Imaging, National University Hospital, National University Health System, Singapore.

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May 2018

Neck-Tongue Syndrome: An Underrecognized Childhood Onset Cephalalgia.

J Child Neurol 2018 04 16;33(5):347-350. Epub 2018 Feb 16.

2 Department of Pediatric Neurology, Evelina Children's Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, UK.

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http://journals.sagepub.com/doi/10.1177/0883073818756681
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http://dx.doi.org/10.1177/0883073818756681DOI Listing
April 2018

Unusual Presentations of Dystrophinopathies in Childhood.

Pediatrics 2018 04;141(Suppl 5):S510-S514

Department of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's and St Thomas' Hospital National Health Service Foundation Trust, London, United Kingdom;

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http://pediatrics.aappublications.org/lookup/doi/10.1542/ped
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http://dx.doi.org/10.1542/peds.2017-2391DOI Listing
April 2018

Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya.

Neurology 2018 02;90(9):e763-e770

From the Clinical Neurosciences Section (S.C.T.-C., F.K., V.G.), UCL Great Ormond Street Institute of Child Health; Neurosurgery Department (D.T.) and Neurology Department (D.S., V.G.), Great Ormond Street Hospital for Children NHS Foundation Trust, London; Neurology Department (S.A.), Birmingham Children's Hospital NHS Foundation Trust; Institute of Neuroscience (A.B.), Newcastle University; Department of Paediatric Neurology (A.B.), Newcastle upon Tyne Hospitals NHS Foundation Trust; Department of Paediatric Neurology (M.C.), Cambridge University Hospitals NHS Foundation Trust; Department of Paediatric Neurology (G.C.), Nottingham University Hospitals NHS Foundation Trust; Department of Paediatric Neurology (F.G.), University Hospital of Wales; Neurology Department (A.H.), Sheffield Children's Hospital NHS Foundation Trust; Neurology Department (K.K.T.), Royal Hospital for Sick Children, Edinburgh; Department of Paediatric Neurology (F.K.), University Hospital Southampton NHS Foundation Trust; Neurology Department (R.K.), Alder Hey Children's NHS Foundation Trust, Liverpool; Department of Paediatric Neurology (H.M.), The Leeds Teaching Hospitals NHS Trust; Department of Paediatric Neurology (L.M.), St Mary's Hospital, Imperial College Healthcare NHS Trust, London; Neurology Department (G.V.), Royal Manchester Children's Hospital, Central Manchester University Hospitals NHS Foundation Trust; Neurology Department (K.V.), Bristol Royal Hospital for Children, University Hospitals Bristol NHS Foundation Trust; Neurology Department (E.W.), Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK; and Department of Paediatrics (T.H.Y.), KK Women's and Children's Hospital, Singapore.

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http://dx.doi.org/10.1212/WNL.0000000000005026DOI Listing
February 2018

Management and outcomes of cochlear implantation in patients with congenital cytomegalovirus (cCMV)-related deafness.

Cochlear Implants Int 2017 07 9;18(4):216-225. Epub 2017 May 9.

a Department of Paediatric Otolaryngology , Evelina London Children's Hospital , London , UK.

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http://dx.doi.org/10.1080/14670100.2017.1315510DOI Listing
July 2017

An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities.

Sci Signal 2016 07 5;9(435):ra68. Epub 2016 Jul 5.

Department of Paediatric Neurology, Neuromuscular Service, Evelina Children's Hospital, St Thomas' Hospital, London SE1 7EH, UK. Randall Division of Cell and Molecular Biophysics, Muscle Signalling Section, King's College, London SE1 1UL, UK. Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE5 9RX, UK.

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http://dx.doi.org/10.1126/scisignal.aad9813DOI Listing
July 2016

Surgery for scoliosis in Duchenne muscular dystrophy.

Cochrane Database Syst Rev 2015 Oct 1(10):CD005375. Epub 2015 Oct 1.

Department of Pediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam Road, Hong Kong SAR, China.

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http://dx.doi.org/10.1002/14651858.CD005375.pub4DOI Listing
October 2015

Diagnostic delays in paediatric stroke.

J Neurol Neurosurg Psychiatry 2015 Aug 23;86(8):917-21. Epub 2014 Oct 23.

Neurosciences Unit, UCL Institute of Child Health, London, UK School of Clinical Sciences, University of Bristol, Bristol, UK.

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http://jnnp.bmj.com/content/early/2014/10/23/jnnp-2014-30918
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http://jnnp.bmj.com/lookup/doi/10.1136/jnnp-2014-309188
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http://dx.doi.org/10.1136/jnnp-2014-309188DOI Listing
August 2015

Guillain-Barré syndrome associated with CASPR2 antibodies: two paediatric cases.

J Peripher Nerv Syst 2014 Sep;19(3):246-9

Department of Clinical Neurosciences, Institute of Psychiatry, King's College London, London, UK.

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http://dx.doi.org/10.1111/jns.12089DOI Listing
September 2014

Childhood arterial ischaemic stroke incidence, presenting features, and risk factors: a prospective population-based study.

Lancet Neurol 2014 Jan 2;13(1):35-43. Epub 2013 Dec 2.

Neurosciences Unit, UCL Institute of Child Health, London, UK; School of Clinical Sciences, University of Bristol, Bristol, UK. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(13)70290-4DOI Listing
January 2014

Episodic ataxia type 1 without episodic ataxia: the diagnostic utility of nerve excitability studies in individuals with KCNA1 mutations.

Dev Med Child Neurol 2013 Oct 5;55(10):959-62. Epub 2013 Aug 5.

Department of Neurology and Neurophysiology, St Thomas' Hospital, Guy's and St Thomas' NHS Foundation Trust, King's Health Partners Academic Health Science Centre, London, UK; Institute of Neurology, University College London, Queen Square, London, UK.

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http://dx.doi.org/10.1111/dmcn.12236DOI Listing
October 2013

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene.

Neuromuscul Disord 2013 May 18;23(5):391-8. Epub 2013 Mar 18.

Department of Paediatric Neurology-Neuromuscular Service, Evelina Children's Hospital, Guy's & St. Thomas' NHS Foundation Trust, UK.

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http://dx.doi.org/10.1016/j.nmd.2013.02.001DOI Listing
May 2013

Surgery for scoliosis in Duchenne muscular dystrophy.

Cochrane Database Syst Rev 2013 Feb 28(2):CD005375. Epub 2013 Feb 28.

Department of Pediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China.

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http://dx.doi.org/10.1002/14651858.CD005375.pub3DOI Listing
February 2013

Beneficial use of steroids in hereditary neuropathy with liability to pressure palsy.

Dev Med Child Neurol 2012 Feb 18;54(2):183-6. Epub 2011 Nov 18.

Department of Paediatric Neurology, Evelina Children's Hospital, Guy's and St Thomas' Hospitals NHS Foundation Trust, London, UK.

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http://dx.doi.org/10.1111/j.1469-8749.2011.04131.xDOI Listing
February 2012

King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene.

Neuromuscul Disord 2011 Jun 22;21(6):420-7. Epub 2011 Apr 22.

Division of Pediatric Neurology, Pediatric Neuromuscular Clinic, 5328 BSRB, 109 Zina Pitcher Place, Ann Arbor, MI, USA.

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http://dx.doi.org/10.1016/j.nmd.2011.03.006DOI Listing
June 2011

Congenital lower brachial plexus palsy due to cervical ribs.

Dev Med Child Neurol 2011 Feb;53(2):188-90

Department of Paediatric Neurology, Evelina Children's and St Thomas' Hospitals, London, UK.

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http://dx.doi.org/10.1111/j.1469-8749.2010.03841.xDOI Listing
February 2011

Basilar artery dolichoectasia in childhood: evidence of vascular compromise.

Childs Nerv Syst 2011 Jan 28;27(1):193-6. Epub 2010 Aug 28.

Department of Paediatric Neurology, Southampton General Hospital, Southampton, UK.

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http://dx.doi.org/10.1007/s00381-010-1267-yDOI Listing
January 2011

Infantile onset myofibrillar myopathy due to recessive CRYAB mutations.

Neuromuscul Disord 2011 Jan 3;21(1):37-40. Epub 2010 Dec 3.

Department of Paediatric Neurology, Neuromuscular Service, Evelina Children's Hospital, London, UK.

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http://dx.doi.org/10.1016/j.nmd.2010.11.003DOI Listing
January 2011

Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin.

Neuromuscul Disord 2010 Nov 10;20(11):709-11. Epub 2010 Jul 10.

Department of Paediatric Neurology, Neuromuscular Service, Evelina Children's Hospital, St. Thomas' Hospital, Lambeth Palace Road, London, UK.

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http://dx.doi.org/10.1016/j.nmd.2010.06.003DOI Listing
November 2010

Generalized arterial calcification of infancy: phenotypic spectrum among three siblings including one case without obvious arterial calcifications.

Am J Med Genet A 2009 Mar;149A(3):456-60

Department of Paediatric Neurology, Evelina Children's Hospital, St Thomas' Hospital, London, UK.

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http://dx.doi.org/10.1002/ajmg.a.32646DOI Listing
March 2009

Neurocysticercosis masquerading as a cerebral infarct.

J Child Neurol 2003 Apr;18(4):298-300

Department of Paediatric Neurology, Guy's and St Thomas' Trust, London, England.

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http://jcn.sagepub.com/content/18/4/298.full.pdf
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http://dx.doi.org/10.1177/08830738030180040501DOI Listing
April 2003