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Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

The Lancet (British edition), 2013-07, Vol.382 (9888), p.223-233

2013

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Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol)

BMC pediatrics, 2011-12, Vol.11 (1), p.120-120, Article 120

2011

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Imaging of Perinatal Stroke

Magnetic resonance imaging clinics of North America, 2012-02, Vol.20 (1), p.1-33

2012

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Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children

Pediatric radiology, 2005-11, Vol.35 (11), p.1086-1091

2005

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Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features

Multiple sclerosis, 2013-01, Vol.19 (1), p.76-86

2013

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Diagnostic accuracy and limitations of post-mortem MRI for neurological abnormalities in fetuses and children

Clinical radiology, 2015-08, Vol.70 (8), p.872-880

2015

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Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children

European radiology, 2014-11, Vol.24 (11), p.2876-2884

2014

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Diagnostic accuracy of postmortem MRI for musculoskeletal abnormalities in fetuses and children

Prenatal diagnosis, 2014-12, Vol.34 (13), p.1254-1261

2014

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CT and MRI appearances of inflammatory pseudotumour of the cervical lymph nodes

British journal of radiology, 2005-07, Vol.78 (931), p.651-654

2005

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Novel surface features for automated detection of focal cortical dysplasias in paediatric epilepsy

NeuroImage clinical, 2017-01, Vol.14 (C), p.18-27

2017

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Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

Brain (London, England : 1878), 2013-02, Vol.136 (Pt 2), p.536-548

2013

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MRI profiling of focal cortical dysplasia using multi‐compartment diffusion models

Epilepsia (Copenhagen), 2020-03, Vol.61 (3), p.433-444

2020

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Quantitative MRI susceptibility mapping reveals cortical signatures of changes in iron, calcium and zinc in malformations of cortical development in children with drug-resistant epilepsy

NeuroImage (Orlando, Fla.), 2021-09, Vol.238, p.118102, Article 118102

2021

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Oxygen dependency of mitochondrial metabolism indicates outcome of newborn brain injury

Journal of cerebral blood flow and metabolism, 2019-10, Vol.39 (10), p.2035-2047

2019

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Magnetic resonance imaging findings in Kenyans and South Africans with active convulsive epilepsy: An observational study

Epilepsia (Copenhagen), 2024-01, Vol.65 (1), p.165-176

2024

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Are children with acute arterial ischaemic stroke eligible for hyperacute thrombolysis? A retrospective audit from a tertiary UK centre

Developmental medicine and child neurology, 2015-02, Vol.57 (2), p.181-186

2015

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Muscle “islands”: An MRI signature distinguishing neurogenic from myopathic causes of early onset distal weakness

Neuromuscular disorders : NMD, 2022-02, Vol.32 (2), p.142-149

2022

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Incidence of cavernoma development in children after radiotherapy for brain tumors

Journal of neurosurgery, 2007-05, Vol.106 (5 Suppl), p.379

2007

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Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

NeuroImage clinical, 2017-01, Vol.15, p.95-105

2017

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RARS2 mutations in a sibship with infantile spasms

Epilepsia (Copenhagen), 2016-05, Vol.57 (5), p.e97-e102

2016

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HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase

Orphanet journal of rare diseases, 2013-12, Vol.8 (1), p.188-188, Article 188

2013

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Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome

Developmental medicine and child neurology, 2013-09, Vol.55 (9), p.846-856

2013

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Fourth ventricle rosette-forming glioneuronal tumour in children: an unusual presentation in an 8-year-old patient, discussion and review of the literature

Child's nervous system, 2013-05, Vol.29 (5), p.839-847

2013

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Skull base osteomyelitis and potential cerebrovascular complications in children

Pediatric radiology, 2012-07, Vol.42 (7), p.867-874

2012

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RARS 2 mutations in a sibship with infantile spasms

Epilepsia (Copenhagen), 2016-05, Vol.57 (5)

2016

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Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

Post mortem magnetic resonance imaging in the fetus, infant and child: a comparative study with conventional autopsy (MaRIAS Protocol)

Imaging of Perinatal Stroke

Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children

Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features

Diagnostic accuracy and limitations of post-mortem MRI for neurological abnormalities in fetuses and children

Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children

Diagnostic accuracy of postmortem MRI for musculoskeletal abnormalities in fetuses and children

CT and MRI appearances of inflammatory pseudotumour of the cervical lymph nodes

Novel surface features for automated detection of focal cortical dysplasias in paediatric epilepsy

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

MRI profiling of focal cortical dysplasia using multi‐compartment diffusion models

Quantitative MRI susceptibility mapping reveals cortical signatures of changes in iron, calcium and zinc in malformations of cortical development in children with drug-resistant epilepsy

Oxygen dependency of mitochondrial metabolism indicates outcome of newborn brain injury

Magnetic resonance imaging findings in Kenyans and South Africans with active convulsive epilepsy: An observational study

Are children with acute arterial ischaemic stroke eligible for hyperacute thrombolysis? A retrospective audit from a tertiary UK centre

Muscle “islands”: An MRI signature distinguishing neurogenic from myopathic causes of early onset distal weakness

Incidence of cavernoma development in children after radiotherapy for brain tumors

Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

RARS2 mutations in a sibship with infantile spasms

HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase

Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome

Fourth ventricle rosette-forming glioneuronal tumour in children: an unusual presentation in an 8-year-old patient, discussion and review of the literature

Skull base osteomyelitis and potential cerebrovascular complications in children

RARS 2 mutations in a sibship with infantile spasms

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