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SEPN1-related myopathies: clinical course in a large cohort of patients

Neurology, 2011-06, Vol.76 (24), p.2073

2011

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Intralabyrinthine Schwannomas: Imaging Diagnosis and Classification

American journal of neuroradiology : AJNR, 2012-01, Vol.33 (1), p.104-109

2012

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Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting

Pediatric radiology, 2024-01, Vol.54 (1), p.117-126

2024

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Subdural haematoma and effusion in infancy: an epidemiological study

Archives of disease in childhood, 2005-09, Vol.90 (9), p.952-955

2005

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Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene

Neurology, 2006-11, Vol.67 (9), p.1710

2006

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Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 gene

Neuropediatrics, 2007-12, Vol.38 (6), p.313

2007

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PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

Molecular genetics and metabolism, 2014-06, Vol.112 (2), p.183-189

2014

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Magnetic resonance imaging of the infant brain: anatomical characteristics and clinical significance of punctate lesions

Archives of disease in childhood. Fetal and neonatal edition, 2002-05, Vol.86 (3), p.F171

2002

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On the receiving end V: Patient perceptions of the side effects of cancer chemotherapy in 1993

Annals of oncology, 1996-02, Vol.7 (2), p.189-195

1996

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Differential induction of PPAR-gamma by luminal glutamine and iNOS by luminal arginine in the rodent postischemic small bowel

American journal of physiology: Gastrointestinal and liver physiology, 2006-04, Vol.290 (4), p.G616-G623

2006

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Neurovascular compression of the trigeminal and glossopharyngeal nerve: three case reports

Archives of disease in childhood, 2000-04, Vol.82 (4), p.311-315

2000

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Endocrine and Bone Monitoring in Boys with Duchenne Muscular Dystrophy; Do we adhere to the standards of care?

Journal of neuromuscular diseases, 2023-01, Vol.10 (6), p.1143-1144

2023

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Surface Morphology of Poly(caprolactone)-b-poly(dimethylsiloxane)-b-poly(caprolactone) Copolymers: Effects on Protein Adsorption

Biomacromolecules, 2001, Vol.2 (2), p.526-537

2001

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MANNA: Just Enough for the Day

The American journal of geriatric psychiatry, 2024-05, Vol.32 (5), p.653-653

Childs, Jeanne

2024

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Cerebral Maturation in Premature Infants: Quantitative Assessment Using MR Imaging

American journal of neuroradiology : AJNR, 2001-09, Vol.22 (8), p.1577-1582

2001

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Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Journal of medical economics, 2022, Vol.25 (1), p.808-816

2022

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Small particle growth in silane radio-frequency discharges

Journal of applied physics, 2000-02, Vol.87 (3), p.1076-1085

2000

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MR features of developing periventricular white matter in preterm infants: evidence of glial cell migration

American journal of neuroradiology : AJNR, 1998-05, Vol.19 (5), p.971-976

1998

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Hospice provision and usage amongst young people with neuromuscular disease in the United Kingdom

European journal of paediatric neurology, 2011-07, Vol.15 (4), p.326-330

2011

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P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S13-S13

2014

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Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar Database

JAMA neurology, 2019-06, Vol.76 (6), p.701

2019

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Reversible simulation of bipartite product Hamiltonians

IEEE transactions on information theory, 2004-06, Vol.50 (6), p.1189-1197

2004

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Any AND-OR Formula of Size N Can Be Evaluated in Time $N^{1/2+o(1)}$ on a Quantum Computer

SIAM journal on computing, 2010-01, Vol.39 (6), p.2513-2530

2010

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Magnetic Resonance and Cranial Ultrasound Characteristics of Periventricular White Matter Abnormalities in Newborn Infants

Clinical radiology, 2001-08, Vol.56 (8), p.647-655

2001

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P67 SEPN1 related myopathies: Clinical course in a large cohort of patients

Neuromuscular disorders : NMD, 2011, Vol.21, p.S26-S26

2011

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SEPN1-related myopathies: clinical course in a large cohort of patients

Intralabyrinthine Schwannomas: Imaging Diagnosis and Classification

Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting

Subdural haematoma and effusion in infancy: an epidemiological study

Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene

Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 gene

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

Magnetic resonance imaging of the infant brain: anatomical characteristics and clinical significance of punctate lesions

On the receiving end V: Patient perceptions of the side effects of cancer chemotherapy in 1993

Differential induction of PPAR-gamma by luminal glutamine and iNOS by luminal arginine in the rodent postischemic small bowel

Neurovascular compression of the trigeminal and glossopharyngeal nerve: three case reports

Endocrine and Bone Monitoring in Boys with Duchenne Muscular Dystrophy; Do we adhere to the standards of care?

Surface Morphology of Poly(caprolactone)-b-poly(dimethylsiloxane)-b-poly(caprolactone) Copolymers: Effects on Protein Adsorption

MANNA: Just Enough for the Day

Cerebral Maturation in Premature Infants: Quantitative Assessment Using MR Imaging

Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Small particle growth in silane radio-frequency discharges

MR features of developing periventricular white matter in preterm infants: evidence of glial cell migration

Hospice provision and usage amongst young people with neuromuscular disease in the United Kingdom

P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar Database

Reversible simulation of bipartite product Hamiltonians

Any AND-OR Formula of Size N Can Be Evaluated in Time $N^{1/2+o(1)}$ on a Quantum Computer

Magnetic Resonance and Cranial Ultrasound Characteristics of Periventricular White Matter Abnormalities in Newborn Infants

P67 SEPN1 related myopathies: Clinical course in a large cohort of patients

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