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Consensus statement: evaluation of new and existing therapeutics for pediatric multiple sclerosis

Multiple sclerosis, 2012-01, Vol.18 (1), p.116-127

2012

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Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome

European journal of neurology, 2018-05, Vol.25 (5), p.782-786

2018

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Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort

Journal of neurology, neurosurgery and psychiatry, 2014-04, Vol.85 (4), p.456-461

2014

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Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)

Neurology, 2008-04, Vol.70 (18), p.1623-1629

2008

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A New Approach to Parallel Processing

IEEE access, 2020, Vol.8, p.30287-30305

2020

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G331(P) Sibling-pair with Mitofusin 2 mutation

Archives of disease in childhood, 2014-04, Vol.99 (Suppl 1), p.A136-A136

2014

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Genotype-phenotype correlation in vanishing white matter disease

Neurology, 2010-10, Vol.75 (17), p.1555-1559

2010

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Headaches – did you sleep well?

Archives of disease in childhood, 2011-04, Vol.96 (Suppl 1), p.A41-A41

2011

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MRI as diagnostic tool in early-onset peroxisomal disorders

Neurology, 2012-04, Vol.78 (17), p.1304-1308

2012

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Paediatric multiple sclerosis: examining utility of the McDonald 2010 criteria

Multiple sclerosis, 2012-05, Vol.18 (5), p.679-682

2012

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Long-term outcomes of NMDAR-Ab encephalitis in U.K. cases

European journal of paediatric neurology, 2017-06, Vol.21, p.e7-e8

2017

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Severe acute disseminated encephalomyelitis: a paediatric intensive care population-based study

Multiple sclerosis, 2011-10, Vol.17 (10), p.1258-1261

2011

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Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease

Molecular genetics and metabolism, 2011-12, Vol.104 (4), p.637-643

2011

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1521 Paediatric Narcolepsy: A Video Series

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A431-A431

2012

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Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSG

Neurology, 2019-10, Vol.93 (14), p.647-647

2019

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P11 Investigation into paediatric N-methyl-D-aspartate receptor (NMDAR) encephalitis: results of the British Paediatric Neurological Surveillance Unit (BPNSU) study

Archives of disease in childhood, 2014-04, Vol.99 (Suppl 1), p.A5-A5

2014

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A rare case presentation of pure neural leprosy

European journal of paediatric neurology, 2017-06, Vol.21, p.e222-e222

2017

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1513 East or Sesame Syndrome: A Case Series

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A429-A429

2012

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G66(P) Interesting cases of pyridoxine dependent epilepsy in late childhood

Archives of disease in childhood, 2015-04, Vol.100 (Suppl 3), p.A28-A28

2015

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PP08.4 – 2929: Relapsing central nervous system demyelination in children with myelin oligodendrocyte glycoprotein (MOG) antibodies

European journal of paediatric neurology, 2015-05, Vol.19, p.S61-S61

2015

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Acute disseminated encephalomyelitis: A review of 18 cases in childhood

Journal of paediatrics and child health, 2003-07, Vol.39 (5), p.336-342

2003

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E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

European journal of paediatric neurology, 2020-11, Vol.29, p.2-13

2020

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Acute disseminated encephalomyelitis: recognition in the hands of general paediatricians

Archives of Disease in Childhood, 2003-02, Vol.88 (2), p.122-124

2003

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PP12.11 – 2550: Atypical forms of 4H leukodystrophy

European journal of paediatric neurology, 2015-05, Vol.19, p.S80-S80

2015

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E.U. paediatric MOG consortium consensus: Part 5 – Treatment of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

European journal of paediatric neurology, 2020-11, Vol.29, p.41-53

2020

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Consensus statement: evaluation of new and existing therapeutics for pediatric multiple sclerosis

Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome

Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)

A New Approach to Parallel Processing

G331(P) Sibling-pair with Mitofusin 2 mutation

Genotype-phenotype correlation in vanishing white matter disease

Headaches – did you sleep well?

MRI as diagnostic tool in early-onset peroxisomal disorders

Paediatric multiple sclerosis: examining utility of the McDonald 2010 criteria

Long-term outcomes of NMDAR-Ab encephalitis in U.K. cases

Severe acute disseminated encephalomyelitis: a paediatric intensive care population-based study

Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease

1521 Paediatric Narcolepsy: A Video Series

Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSG

P11 Investigation into paediatric N-methyl-D-aspartate receptor (NMDAR) encephalitis: results of the British Paediatric Neurological Surveillance Unit (BPNSU) study

A rare case presentation of pure neural leprosy

1513 East or Sesame Syndrome: A Case Series

G66(P) Interesting cases of pyridoxine dependent epilepsy in late childhood

PP08.4 – 2929: Relapsing central nervous system demyelination in children with myelin oligodendrocyte glycoprotein (MOG) antibodies

Acute disseminated encephalomyelitis: A review of 18 cases in childhood

E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

Acute disseminated encephalomyelitis: recognition in the hands of general paediatricians

PP12.11 – 2550: Atypical forms of 4H leukodystrophy

E.U. paediatric MOG consortium consensus: Part 5 – Treatment of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

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