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European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 18, 2004
Predictors of mortality and neurological morbidity in children undergoing extracorporeal life support for cardiac disease
Gabriel Chow, Bhagawan Koirala, Derek Armstrong, et al.
The British Journal of Radiology
|
April 25, 2018
Evaluation of an internet-based animated preparatory video for children undergoing non-sedated MRI
Hannah L McGlashan, Rob A Dineen, Sofia Szeszak, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
March 3, 2011
Insight into on-wafer crystallization of pure-silica-zeolite films through nutrient replenishment
Christopher M Lew, Yan Liu, David Kisailus, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 6, 2022
Quality of life and neurological disability in children and young people with ataxia telangiectasia
Hannah L McGlashan, Caroline V Blanchard, Celia Luscombe, et al.
Neuroimage. Clinical
|
December 20, 2019
Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia
Rob A Dineen, Felix Raschke, Hannah L McGlashan, et al.
Journal of Neuromuscular Diseases
|
January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain
Nikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
December 20, 2013
Neurological manifestations of influenza infection in children and adults: results of a National British Surveillance Study
Anu Goenka, Benedict D Michael, Elizabeth Ledger, et al.
Neurology
|
February 28, 2018
Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya
Sara C Tho-Calvi, Dominic Thompson, Dawn Saunders, et al.
Neuromuscular Disorders : NMD
|
March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
American Journal of Human Genetics
|
December 3, 2015
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain
Clare V Logan, Judith Cossins, Pedro M Rodríguez Cruz, et al.
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Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 18, 2004
Predictors of mortality and neurological morbidity in children undergoing extracorporeal life support for cardiac disease
Gabriel Chow, Bhagawan Koirala, Derek Armstrong, et al.
The British Journal of Radiology
|
April 25, 2018
Evaluation of an internet-based animated preparatory video for children undergoing non-sedated MRI
Hannah L McGlashan, Rob A Dineen, Sofia Szeszak, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
March 3, 2011
Insight into on-wafer crystallization of pure-silica-zeolite films through nutrient replenishment
Christopher M Lew, Yan Liu, David Kisailus, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 6, 2022
Quality of life and neurological disability in children and young people with ataxia telangiectasia
Hannah L McGlashan, Caroline V Blanchard, Celia Luscombe, et al.
Neuroimage. Clinical
|
December 20, 2019
Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia
Rob A Dineen, Felix Raschke, Hannah L McGlashan, et al.
Journal of Neuromuscular Diseases
|
January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain
Nikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
December 20, 2013
Neurological manifestations of influenza infection in children and adults: results of a National British Surveillance Study
Anu Goenka, Benedict D Michael, Elizabeth Ledger, et al.
Neurology
|
February 28, 2018
Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya
Sara C Tho-Calvi, Dominic Thompson, Dawn Saunders, et al.
Neuromuscular Disorders : NMD
|
March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
American Journal of Human Genetics
|
December 3, 2015
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain
Clare V Logan, Judith Cossins, Pedro M Rodríguez Cruz, et al.
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of 3