Publications by authors named "Karine Lascelles"

29Publications

Ischemic Stroke Following Ergotamine Overdose.

Pediatr Neurol 2019 12 6;101:81-82. Epub 2019 Aug 6.

Department of Paediatric Neurosciences, Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, King's Health Partners AHSC, London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2019.07.016DOI Listing
December 2019

Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis.

Mult Scler 2020 03 7;26(3):333-342. Epub 2019 Feb 7.

Department of Paediatric Neurology, Great Ormond Street Hospital for Children, London, UK; Department of Neuroinflammation, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK.

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http://journals.sagepub.com/doi/10.1177/1352458518823486
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http://dx.doi.org/10.1177/1352458518823486DOI Listing
March 2020

Further refinement of COL4A1 and COL4A2 related cortical malformations.

Eur J Med Genet 2018 Dec 11;61(12):765-772. Epub 2018 Oct 11.

Paris Descartes - Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute, Paris, France; Pediatric Neurology, APHP- Necker Enfants Malades Hospital, Paris, France; National Rare Disease Center- Centre de Référence "Déficiences Intellectuelles de Causes Rares", AP-HP, Necker Enfants Malades, 75015, Paris, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212173084
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http://dx.doi.org/10.1016/j.ejmg.2018.10.004DOI Listing
December 2018

Cerebral vasculopathy in childhood neurofibromatosis type 2: cause for concern?

Dev Med Child Neurol 2018 12 21;60(12):1285-1288. Epub 2018 May 21.

Department of Neurology, Great Ormond Street Children's Hospital, London, UK.

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http://dx.doi.org/10.1111/dmcn.13920DOI Listing
December 2018

Clinical and molecular characterization of -related severe early-onset epilepsy.

Neurology 2018 01 1;90(1):e55-e66. Epub 2017 Dec 1.

From Molecular Neurosciences (A.M., E.M., A., A.N., M.A.K.), Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health; Department of Neurology (A.M., A., A.N., C.E., J.H.C., M.A.K.) and Neuroradiology (W.K.C.), Great Ormond Street Hospital for Children, London, UK; Florey Institute of Neuroscience and Mental Health (U.N., E.V.G., I.E.S., S.P.), Melbourne, Australia; Department of Biological Sciences (S.M., M.T.), Institute of Structural and Molecular Biology, Birkbeck College, University of London; Regional Molecular Genetics Laboratory (N.T., R.H.S.), North East Thames Regional Genetics Service, and Department of Clinical Genetics (A.V.K., R.H.S.), Great Ormond Street Hospital, London, UK; Department of Paediatric Neurology (S.A.), Red Cross War Memorial Children's Hospital, Cape Town, South Africa; Department of Paediatric Neurology (G.A.), Addenbrooke's Hospital, Cambridge; Roald Dahl EEG Unit (R.A.), Department of Neurology, and Department of Neurology (R.K.), Alder Hey Children's Hospital, Liverpool; Department of Paediatric Neurology (A.D.), Sheffield Children's Hospital; Clinical Neurosciences (C.E., J.H.C.), Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London; Institute of Infection and Global Health (R.K.), University of Liverpool; Department of Paediatric Neurology (K.L.), Evelina Children's Hospital, Guys and St. Thomas' NHS Foundation Trust, London; Department of Clinical Genetics (T.M.), Northern Genetics Service; Department of Pediatric Neurology (V.R.), Great North Children's Hospital, Newcastle Upon Tyne; Department of Paediatric Neurology (R.S.), University Hospital Leicester Children's Hospital; Department of Paediatric Neurology (J.T.), Royal Manchester Children's Hospital; Department of Paediatric Neurology (W.W.), Nottingham University Hospitals NHS Trust, UK; Epilepsy Genetics Program (A. Poduri), Department of Neurology, Boston Children's Hospital; Department of Neurology (A. Poduri), Harvard Medical School, Boston, MA; University of Melbourne (I.E.S.), Austin Health and Royal Children's Hospital, Australia; and Department of Medicine (S.P.), Royal Melbourne Hospital, University of Melbourne, Australia. Dr. Malhotra is currently at the Department of Biochemistry, University of Cambridge, UK.

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http://dx.doi.org/10.1212/WNL.0000000000004762DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754647PMC
January 2018

Neurofibroma of the cervical spine in infants.

Childs Nerv Syst 2016 Dec 26;32(12):2277-2279. Epub 2016 Sep 26.

Department of Paediatric and Adult Neurosurgery, King's College Hospital NHS Foundation Trust, Denmark Hill, London, SE5 9RS, UK.

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http://dx.doi.org/10.1007/s00381-016-3253-5DOI Listing
December 2016

Reversible vigabatrin-induced life-threatening encephalopathy.

JAMA Neurol 2014 Jan;71(1):108-9

Department of Paediatric Neurosciences, Evelina Children's Hospital, St Thomas' Hospital, King's Health Partners Academic Health Science Centre, London, England.

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http://dx.doi.org/10.1001/jamaneurol.2013.1858DOI 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

Atypical presentation of neuropsychiatric lupus with acanthosis nigricans.

Pediatr Neurol 2012 Oct;47(4):291-4

Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hopitaux de Paris, Paris Descartes University, Paris, France.

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http://dx.doi.org/10.1016/j.pediatrneurol.2012.06.005DOI Listing
October 2012

Neurodevelopmental movement disorders - an update on childhood motor stereotypies.

Dev Med Child Neurol 2011 Nov 12;53(11):979-85. Epub 2011 Jul 12.

King's College London School of Medicine, London.

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http://dx.doi.org/10.1111/j.1469-8749.2011.04058.xDOI Listing
November 2011

Encephalopathy and SCN1A mutations.

Epilepsia 2011 Apr 22;52(4):e26-30. Epub 2011 Mar 22.

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

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http://dx.doi.org/10.1111/j.1528-1167.2011.03019.xDOI Listing
April 2011

Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase.

Seizure 2008 Oct 5;17(7):658-64. Epub 2008 Mar 5.

Service de Neurologie Pediatrique et Maladies Metaboliques, Departement de Pediatrie, Hopital Necker Enfants Malades, AP-HP, Université Paris Descartes, Paris, France.

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http://linkinghub.elsevier.com/retrieve/pii/S105913110800033
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http://dx.doi.org/10.1016/j.seizure.2008.01.005DOI Listing
October 2008