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C DeVile

Showing results (1-10 of 9) with videos related to

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BJA Education|May 1, 2023
Osteogenesis imperfectaE Chan, C DeVile, V S Ratnamma
Journal of Inherited Metabolic Disease|September 19, 2007
A severity scoring tool to assess the neurological features of neuronopathic Gaucher diseaseE H Davies, R Surtees, C DeVile, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
What's new in neuro-oncologyC Devile, R Packer, D Walker, et al.
Clinical Radiology|January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosisS J Counsell, C Devile, E Mercuri, et al.
Lancet (London, England)|May 16, 2003
Neonatal epileptic encephalopathyP T Clayton, R A H Surtees, C DeVile, et al.
Neuropediatrics|November 9, 2000
Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?E Mercuri, C A Sewry, S C Brown, et al.
Neuromuscular Disorders : NMD|August 4, 2018
Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathyA Silwal, M Pitt, R Phadke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Bone|November 7, 2016
Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfectaM Balasubramanian, J Hurst, S Brown, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
BJA Education|May 1, 2023
Osteogenesis imperfectaE Chan, C DeVile, V S Ratnamma
Journal of Inherited Metabolic Disease|September 19, 2007
A severity scoring tool to assess the neurological features of neuronopathic Gaucher diseaseE H Davies, R Surtees, C DeVile, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
What's new in neuro-oncologyC Devile, R Packer, D Walker, et al.
Clinical Radiology|January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosisS J Counsell, C Devile, E Mercuri, et al.
Lancet (London, England)|May 16, 2003
Neonatal epileptic encephalopathyP T Clayton, R A H Surtees, C DeVile, et al.
Neuropediatrics|November 9, 2000
Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?E Mercuri, C A Sewry, S C Brown, et al.
Neuromuscular Disorders : NMD|August 4, 2018
Clinical spectrum, treatment and outcome of children with suspected diagnosis of chronic inflammatory demyelinating polyradiculoneuropathyA Silwal, M Pitt, R Phadke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Bone|November 7, 2016
Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfectaM Balasubramanian, J Hurst, S Brown, et al.
Pageof 1