Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Manju A Kurian

Showing results (1-10 of 172) with videos related to

Pageof 18
Sort By:
Frontiers in Molecular Neuroscience|September 23, 2016
Utility of Induced Pluripotent Stem Cells for the Study and Treatment of Genetic Diseases: Focus on Childhood Neurological DisordersSerena Barral, Manju A Kurian
Current Opinion in Neurology|July 14, 2020
Recent genetic advances in early-onset dystoniaDora Steel, Manju A Kurian
Developmental Medicine and Child Neurology|March 27, 2014
Genetic disorders of thyroid metabolism and brain developmentManju A Kurian, Heinz Jungbluth
Journal of Inherited Metabolic Disease|June 28, 2018
Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanismsLucia Abela, Manju A Kurian
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2015
Benign Hereditary Chorea: An UpdateKathryn J Peall, Manju A Kurian
International Review of Neurobiology|November 12, 2013
Pantothenate kinase-associated neurodegeneration (PKAN) and PLA2G6-associated neurodegeneration (PLAN): review of two major neurodegeneration with brain iron accumulation (NBIA) phenotypesManju A Kurian, Susan J Hayflick
Continuum (Minneapolis, Minn.)|August 7, 2016
Movement Disorders Presenting in ChildhoodManju A Kurian, Russell C Dale
Journal of Inherited Metabolic Disease|April 4, 2014
What is new for monoamine neurotransmitter disorders?Clara Marecos, Joanne Ng, Manju A Kurian
Annual Review of Genomics and Human Genetics|May 15, 2015
Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological MechanismsEsther Meyer, Manju A Kurian, Susan J Hayflick
Handbook of Clinical Neurology|January 13, 2018
Neurodegeneration with brain iron accumulationSusan J Hayflick, Manju A Kurian, Penelope Hogarth
Pageof 18

Showing results (1-10 of 172) with videos related to

Sort By:
Pageof 18
Frontiers in Molecular Neuroscience|September 23, 2016
Utility of Induced Pluripotent Stem Cells for the Study and Treatment of Genetic Diseases: Focus on Childhood Neurological DisordersSerena Barral, Manju A Kurian
Current Opinion in Neurology|July 14, 2020
Recent genetic advances in early-onset dystoniaDora Steel, Manju A Kurian
Developmental Medicine and Child Neurology|March 27, 2014
Genetic disorders of thyroid metabolism and brain developmentManju A Kurian, Heinz Jungbluth
Journal of Inherited Metabolic Disease|June 28, 2018
Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanismsLucia Abela, Manju A Kurian
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2015
Benign Hereditary Chorea: An UpdateKathryn J Peall, Manju A Kurian
International Review of Neurobiology|November 12, 2013
Pantothenate kinase-associated neurodegeneration (PKAN) and PLA2G6-associated neurodegeneration (PLAN): review of two major neurodegeneration with brain iron accumulation (NBIA) phenotypesManju A Kurian, Susan J Hayflick
Continuum (Minneapolis, Minn.)|August 7, 2016
Movement Disorders Presenting in ChildhoodManju A Kurian, Russell C Dale
Journal of Inherited Metabolic Disease|April 4, 2014
What is new for monoamine neurotransmitter disorders?Clara Marecos, Joanne Ng, Manju A Kurian
Annual Review of Genomics and Human Genetics|May 15, 2015
Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological MechanismsEsther Meyer, Manju A Kurian, Susan J Hayflick
Handbook of Clinical Neurology|January 13, 2018
Neurodegeneration with brain iron accumulationSusan J Hayflick, Manju A Kurian, Penelope Hogarth
Pageof 18