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Mark I Rees

Showing results (31-40 of 82) with videos related to

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Human Molecular Genetics|April 4, 2002
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)Mark I Rees, Trevor M Lewis, John B J Kwok, et al.
BMJ Open|April 4, 2019
Using natural language processing to extract structured epilepsy data from unstructured clinic letters: development and validation of the ExECT (extraction of epilepsy clinical text) systemBeata Fonferko-Shadrach, Arron S Lacey, Angus Roberts, et al.
Heart Rhythm|September 9, 2008
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndromeCarey-Anne Eddy, Judith M MacCormick, Seo-Kyung Chung, et al.
Annals of Emergency Medicine|March 14, 2009
Misdiagnosis of long QT syndrome as epilepsy at first presentationJudith M MacCormick, Hugh McAlister, Jackie Crawford, et al.
Neurology|January 21, 2021
Incidence, Prevalence, and Health Care Outcomes in Idiopathic Intracranial Hypertension: A Population StudyLatif Miah, Huw Strafford, Beata Fonferko-Shadrach, et al.
Journal of Neuroinflammation|June 24, 2016
Complement is activated in progressive multiple sclerosis cortical grey matter lesionsLewis M Watkins, James W Neal, Sam Loveless, et al.
Brain Research. Molecular Brain Research|June 15, 2004
TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's diseaseSuzanne J Reid, Willeke M C van Roon-Mom, Phil C Wood, et al.
Epilepsia|April 16, 2015
Epilepsy and deprivation, a data linkage studyWilliam O Pickrell, Arron S Lacey, Owen G Bodger, et al.
Brain : a Journal of Neurology|September 14, 2013
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delayRhys H Thomas, Seo-Kyung Chung, Sian E Wood, et al.
Epilepsia|May 28, 2021
Epilepsy, antiepileptic drugs, and the risk of major cardiovascular eventsElinor Lee-Lane, Fatemeh Torabi, Arron Lacey, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|April 4, 2002
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)Mark I Rees, Trevor M Lewis, John B J Kwok, et al.
BMJ Open|April 4, 2019
Using natural language processing to extract structured epilepsy data from unstructured clinic letters: development and validation of the ExECT (extraction of epilepsy clinical text) systemBeata Fonferko-Shadrach, Arron S Lacey, Angus Roberts, et al.
Heart Rhythm|September 9, 2008
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndromeCarey-Anne Eddy, Judith M MacCormick, Seo-Kyung Chung, et al.
Annals of Emergency Medicine|March 14, 2009
Misdiagnosis of long QT syndrome as epilepsy at first presentationJudith M MacCormick, Hugh McAlister, Jackie Crawford, et al.
Neurology|January 21, 2021
Incidence, Prevalence, and Health Care Outcomes in Idiopathic Intracranial Hypertension: A Population StudyLatif Miah, Huw Strafford, Beata Fonferko-Shadrach, et al.
Journal of Neuroinflammation|June 24, 2016
Complement is activated in progressive multiple sclerosis cortical grey matter lesionsLewis M Watkins, James W Neal, Sam Loveless, et al.
Brain Research. Molecular Brain Research|June 15, 2004
TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's diseaseSuzanne J Reid, Willeke M C van Roon-Mom, Phil C Wood, et al.
Epilepsia|April 16, 2015
Epilepsy and deprivation, a data linkage studyWilliam O Pickrell, Arron S Lacey, Owen G Bodger, et al.
Brain : a Journal of Neurology|September 14, 2013
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delayRhys H Thomas, Seo-Kyung Chung, Sian E Wood, et al.
Epilepsia|May 28, 2021
Epilepsy, antiepileptic drugs, and the risk of major cardiovascular eventsElinor Lee-Lane, Fatemeh Torabi, Arron Lacey, et al.
Pageof 9