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Adeline Vanderver

Showing results (1-10 of 217) with videos related to

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Molecular Genetics and Metabolism|March 25, 2022
Corrigendum to "Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots" [2017 Nov;122(3):134-139]Adeline Vanderver
Current Neurology and Neuroscience Reports|March 4, 2005
Tools for diagnosis of leukodystrophies and other disorders presenting with white matter diseaseAdeline Vanderver
Continuum (Minneapolis, Minn.)|June 5, 2016
Genetic Leukoencephalopathies in AdultsAdeline Vanderver
Neurology|March 31, 2012
If at first you don't succeed, test again (for peroxisomal biogenesis disorders)Adeline Vanderver
Annals of Neurology|September 25, 2018
Correction to Helman et al (2016) MRI spectrum of SDH deficiency-related infantile leukoencephalopathyGuy Helman, Adeline Vanderver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2022
Response to Leidi et alAdeline Vanderver, Ralf A Husain
Nature Reviews. Neurology|January 6, 2018
Adulthood leukodystrophiesWolfgang Köhler, Julian Curiel, Adeline Vanderver
Handbook of Clinical Neurology|February 27, 2018
The spectrum of adult-onset heritable white-matter disordersGuy Helman, Sunita Venkateswaran, Adeline Vanderver
The New England Journal of Medicine|November 30, 2020
JAK Inhibition in the Aicardi-Goutières Syndrome. ReplyLaura Adang, Raphaela Goldbach-Mansky, Adeline Vanderver
JAMA Neurology|April 5, 2016
Neurologist Comfort in the Use of Next-Generation Sequencing Diagnostics: Current State and Future ProspectsGuy Helman, Joshua L Bonkowsky, Adeline Vanderver
Pageof 22

Showing results (1-10 of 217) with videos related to

Sort By:
Pageof 22
Molecular Genetics and Metabolism|March 25, 2022
Corrigendum to "Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots" [2017 Nov;122(3):134-139]Adeline Vanderver
Current Neurology and Neuroscience Reports|March 4, 2005
Tools for diagnosis of leukodystrophies and other disorders presenting with white matter diseaseAdeline Vanderver
Continuum (Minneapolis, Minn.)|June 5, 2016
Genetic Leukoencephalopathies in AdultsAdeline Vanderver
Neurology|March 31, 2012
If at first you don't succeed, test again (for peroxisomal biogenesis disorders)Adeline Vanderver
Annals of Neurology|September 25, 2018
Correction to Helman et al (2016) MRI spectrum of SDH deficiency-related infantile leukoencephalopathyGuy Helman, Adeline Vanderver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2022
Response to Leidi et alAdeline Vanderver, Ralf A Husain
Nature Reviews. Neurology|January 6, 2018
Adulthood leukodystrophiesWolfgang Köhler, Julian Curiel, Adeline Vanderver
Handbook of Clinical Neurology|February 27, 2018
The spectrum of adult-onset heritable white-matter disordersGuy Helman, Sunita Venkateswaran, Adeline Vanderver
The New England Journal of Medicine|November 30, 2020
JAK Inhibition in the Aicardi-Goutières Syndrome. ReplyLaura Adang, Raphaela Goldbach-Mansky, Adeline Vanderver
JAMA Neurology|April 5, 2016
Neurologist Comfort in the Use of Next-Generation Sequencing Diagnostics: Current State and Future ProspectsGuy Helman, Joshua L Bonkowsky, Adeline Vanderver
Pageof 22