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Lucinda Carr

Showing results (11-20 of 41) with videos related to

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Developmental Medicine and Child Neurology|April 14, 2026
Description actualisée de la paralysie cérébraleBernard Dan, Peter Rosenbaum, Lucinda Carr, et al.
Developmental Medicine and Child Neurology|April 10, 2026
Descrição atualizada da paralisia cerebralBernard Dan, Peter Rosenbaum, Lucinda Carr, et al.
The American Journal of Psychiatry|August 3, 2002
Alcohol and ADH2 in Israel: Ashkenazis, Sephardics, and recent Russian immigrantsDeborah Hasin, Efrat Aharonovich, Xinhua Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2016
SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathyGavin Charlesworth, Bettina Balint, Niccolò E Mencacci, et al.
Alcohol (Fayetteville, N.Y.)|December 1, 2006
ADH1C*2 allele is associated with alcohol dependence and elevated liver enzymes in Trinidad and TobagoKarelia Montane-Jaime, Shelley Moore, Samuel Shafe, et al.
BMJ Open|December 13, 2016
Pay More Attention: a national mixed methods study to identify the barriers and facilitators to ensuring equal access to high-quality hospital care and services for children and young people with and without learning disabilities and their familiesKate Oulton, Jo Wray, Lucinda Carr, et al.
Pediatric Neurology|September 13, 2011
Clinical neuroimaging features and outcome in molybdenum cofactor deficiencyKayal Vijayakumar, Rox Gunny, Stephanie Grunewald, et al.
Neurology|February 25, 2014
ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystoniaUna-Marie Sheerin, Susanne A Schneider, Lucinda Carr, et al.
BMC Health Services Research|March 24, 2018
Mapping staff perspectives towards the delivery of hospital care for children and young people with and without learning disabilities in England: a mixed methods national studyKate Oulton, Faith Gibson, Lucinda Carr, et al.
Neurology|July 8, 2024
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement TherapyRobert Spaull, Audrey K Soo, Spyros Batzios, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Developmental Medicine and Child Neurology|April 14, 2026
Description actualisée de la paralysie cérébraleBernard Dan, Peter Rosenbaum, Lucinda Carr, et al.
Developmental Medicine and Child Neurology|April 10, 2026
Descrição atualizada da paralisia cerebralBernard Dan, Peter Rosenbaum, Lucinda Carr, et al.
The American Journal of Psychiatry|August 3, 2002
Alcohol and ADH2 in Israel: Ashkenazis, Sephardics, and recent Russian immigrantsDeborah Hasin, Efrat Aharonovich, Xinhua Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2016
SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathyGavin Charlesworth, Bettina Balint, Niccolò E Mencacci, et al.
Alcohol (Fayetteville, N.Y.)|December 1, 2006
ADH1C*2 allele is associated with alcohol dependence and elevated liver enzymes in Trinidad and TobagoKarelia Montane-Jaime, Shelley Moore, Samuel Shafe, et al.
BMJ Open|December 13, 2016
Pay More Attention: a national mixed methods study to identify the barriers and facilitators to ensuring equal access to high-quality hospital care and services for children and young people with and without learning disabilities and their familiesKate Oulton, Jo Wray, Lucinda Carr, et al.
Pediatric Neurology|September 13, 2011
Clinical neuroimaging features and outcome in molybdenum cofactor deficiencyKayal Vijayakumar, Rox Gunny, Stephanie Grunewald, et al.
Neurology|February 25, 2014
ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystoniaUna-Marie Sheerin, Susanne A Schneider, Lucinda Carr, et al.
BMC Health Services Research|March 24, 2018
Mapping staff perspectives towards the delivery of hospital care for children and young people with and without learning disabilities in England: a mixed methods national studyKate Oulton, Faith Gibson, Lucinda Carr, et al.
Neurology|July 8, 2024
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement TherapyRobert Spaull, Audrey K Soo, Spyros Batzios, et al.
Pageof 5