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E Craig

Showing results (741-750 of 1,029) with videos related to

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Journal of Diabetes and Its Complications|September 6, 2025
Atypical complications and co-morbidities of type 1 diabetes in young adultsSteven James, Rebecca Barber, Jess Forster, et al.
BMJ Open|September 4, 2021
Electrophysiological ventricular substrate of stroke: a prospective cohort study in the Atherosclerosis Risk in Communities (ARIC) studyJohn A Johnson, Kazi T Haq, Katherine J Lutz, et al.
Plos One|June 21, 2018
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Nature|April 12, 2013
Earliest evidence for the use of potteryO E Craig, H Saul, A Lucquin, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Interventional Neurology|April 2, 2020
Does the Addition of Non-Approved Inclusion and Exclusion Criteria for rtPA Impact Treatment Rates? Findings in Australia, the UK, and the USALouise E Craig, Sandy Middleton, Helen Hamilton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2020
Pedunculopontine Nucleus Microstructure Predicts Postural and Gait Symptoms in Parkinson's DiseaseChesney E Craig, Ned J Jenkinson, John-Stuart Brittain, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaShari Javadiyan, Sionne E M Lucas, Dechen Wangmo, et al.
Pageof 103

Showing results (741-750 of 1,029) with videos related to

Sort By:
Pageof 103
Journal of Diabetes and Its Complications|September 6, 2025
Atypical complications and co-morbidities of type 1 diabetes in young adultsSteven James, Rebecca Barber, Jess Forster, et al.
BMJ Open|September 4, 2021
Electrophysiological ventricular substrate of stroke: a prospective cohort study in the Atherosclerosis Risk in Communities (ARIC) studyJohn A Johnson, Kazi T Haq, Katherine J Lutz, et al.
Plos One|June 21, 2018
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Nature|April 12, 2013
Earliest evidence for the use of potteryO E Craig, H Saul, A Lucquin, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Interventional Neurology|April 2, 2020
Does the Addition of Non-Approved Inclusion and Exclusion Criteria for rtPA Impact Treatment Rates? Findings in Australia, the UK, and the USALouise E Craig, Sandy Middleton, Helen Hamilton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2020
Pedunculopontine Nucleus Microstructure Predicts Postural and Gait Symptoms in Parkinson's DiseaseChesney E Craig, Ned J Jenkinson, John-Stuart Brittain, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaShari Javadiyan, Sionne E M Lucas, Dechen Wangmo, et al.
Pageof 103