Lloyd K. Shield

University Hospital Southampton NHS Foundation Trust — United Kingdom

Medicine · Health Sciences

24h-index2.5kcitations55works0.02yr avg
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Research Topics

Neurogenetic and Muscular Disorders Research(9), Mitochondrial Function and Pathology(6), Muscle Physiology and Disorders(6), Hereditary Neurological Disorders(6), Epilepsy research and treatment(5)

Publications54 total

P006 An evaluation of digital mole mapping for patients at high risk of melanoma
British Journal of Dermatology·2025Open Access
Ian James Hopkins
Child Neurology·2021
Fifty years of paediatric neurology in Australasia
Journal of Paediatrics and Child Health·2016Open Access
234. Early onset severe axonal neuropathy associated with optic atrophy and vocal cord paresis due to a mitofusin 2 mutation
Journal of Clinical Neuroscience·2009
KING-DENBOROUGH SYNDROME CAUSED BY A NOVEL MUTATION IN THE RYANODINE RECEPTOR GENE
Neurology·2008· 51 cited
Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the <i>SMN</i> gene
Muscle & Nerve·2008· 8 cited
Early-onset severe axonal neuropathy associated with optic atrophy and vocal cord paresis due to a mitofusin 2 mutation
Clinical Neurophysiology·2008
Rituximab for treatment of refractory childhood chronic inflammatory demyelinating polyneuropathy
Clinical Neurophysiology·2008· 1 cited
C.P.1.04 Defining diagnostic boundaries for congenital fibre type disproportion
Neuromuscular Disorders·2007· 1 cited
C.P.4.15 King-Denborough syndrome caused by a novel mutation in RYR1
Neuromuscular Disorders·2007
G.O.2 A clinical and pathological study of congenital fibre type disproportion
Neuromuscular Disorders·2006
<i>SEPN1</i>: Associated with congenital fiber‐type disproportion and insulin resistance
Annals of Neurology·2006· 175 cited
Subacute inflammatory demyelinating polyneuropathy in children
Neurology·2005· 20 cited
Neuropsychological outcome after acute disseminated encephalomyelitis: Impact of age at illness onset
Pediatric Neurology·2004· 80 cited
Clinical course correlates poorly with muscle pathology in nemaline myopathy
Neurology·2003· 130 cited
Childhood chronic inflammatory demyelinating polyneuropathy with central nervous system demyelination resembling multiple sclerosis
Neuromuscular Disorders·2003· 30 cited
HHE SYNDROME; CHARACTERISTIC EARLY MAGNETIC RESONANCE IMAGING FINDINGS
2002
Hemiconvulsion-Hemiplegia-Epilepsy Syndrome: Characteristic Early Magnetic Resonance Imaging Findings
Journal of Child Neurology·2002· 59 cited
Nemaline myopathy: A clinical study of 143 cases
Annals of Neurology·2001· 272 cited
Clinical and neuroradiologic features of acute disseminated encephalomyelitis in children
Neurology·2001· 539 cited
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Frequent Co-authors

Andrew J. Kornberg(14), Monique M. Ryan(7), I. J. Hopkins(7), Lee Coleman(6), A. Simon Harvey(5), Xenia Dennett(5), Eppie M. Yiu(5), Kathryn N. North(4), Ian J. Hopkins(4), Padraic J. Grattan‐Smith(4), David W. Boldt(4), Alan H. Beggs(3), Christina Schnell(2), Corinne D. Strickland(2), Susan T. Iannaccone(2), Nigel G. Laing(2), David J. Cook(2), Samuel F. Berkovic(2), Nigel F. Clarke(2), Mark T. Mackay(2)