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

Yanick J Crow

Showing results (41-50 of 233) with videos related to

Pageof 24
Sort By:
Journal of Clinical Immunology|September 7, 2018
A Brief Historical Perspective on the Pathological Consequences of Excessive Type I Interferon Exposure In vivoYanick J Crow, Pierre Lebon, Jean-Laurent Casanova, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Sedaghatian spondylometaphyseal dysplasia with pachygyria and absence of the corpus callosumSharon J English, Neti Gayatri, Rosemary Arthur, et al.
Developmental Medicine and Child Neurology|December 31, 2013
Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypesJohn H Livingston, Stavros Stivaros, Dan Warren, et al.
Medecine Sciences : M/S|April 2, 2019
[Pathological consequences of excess of interferon in vivo]Pierre Lebon, Yanick J Crow, Jean-Laurent Casanova, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|May 6, 2017
MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy SpectrumInsa Buers, Gillian I Rice, Yanick J Crow, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2011
Cerebral vasculopathy is a common feature in Aicardi-Goutieres syndrome associated with SAMHD1 mutationsMarcel du Moulin, Peter Nürnberg, Yanick J Crow, et al.
Indian Journal of Ophthalmology|December 22, 2018
Familial Blau syndrome:First molecularly confirmed report from IndiaMahesh Janarthanan, Chanchal Poddar, S Sudharshan, et al.
Neurology|December 2, 2024
A Rare Genetic Cause of Spastic ParaparesisShakya Bhattacharjee, Rekha Siripurapu, Andrew Swale, et al.
Developmental Medicine and Child Neurology|August 22, 2009
Elevated pterins in cerebral spinal fluid--biochemical marker of Aicardi-Goutières syndromeEvangeline Wassmer, Jaspal Singh, Shakti Agrawal, et al.
Neurology|July 3, 2015
Neuromyelitis optica in a child with Aicardi-Goutières syndromeYael Hacohen, Sameer Zuberi, Angela Vincent, et al.
Pageof 24

Showing results (41-50 of 233) with videos related to

Sort By:
Pageof 24
Journal of Clinical Immunology|September 7, 2018
A Brief Historical Perspective on the Pathological Consequences of Excessive Type I Interferon Exposure In vivoYanick J Crow, Pierre Lebon, Jean-Laurent Casanova, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Sedaghatian spondylometaphyseal dysplasia with pachygyria and absence of the corpus callosumSharon J English, Neti Gayatri, Rosemary Arthur, et al.
Developmental Medicine and Child Neurology|December 31, 2013
Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypesJohn H Livingston, Stavros Stivaros, Dan Warren, et al.
Medecine Sciences : M/S|April 2, 2019
[Pathological consequences of excess of interferon in vivo]Pierre Lebon, Yanick J Crow, Jean-Laurent Casanova, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|May 6, 2017
MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy SpectrumInsa Buers, Gillian I Rice, Yanick J Crow, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2011
Cerebral vasculopathy is a common feature in Aicardi-Goutieres syndrome associated with SAMHD1 mutationsMarcel du Moulin, Peter Nürnberg, Yanick J Crow, et al.
Indian Journal of Ophthalmology|December 22, 2018
Familial Blau syndrome:First molecularly confirmed report from IndiaMahesh Janarthanan, Chanchal Poddar, S Sudharshan, et al.
Neurology|December 2, 2024
A Rare Genetic Cause of Spastic ParaparesisShakya Bhattacharjee, Rekha Siripurapu, Andrew Swale, et al.
Developmental Medicine and Child Neurology|August 22, 2009
Elevated pterins in cerebral spinal fluid--biochemical marker of Aicardi-Goutières syndromeEvangeline Wassmer, Jaspal Singh, Shakti Agrawal, et al.
Neurology|July 3, 2015
Neuromyelitis optica in a child with Aicardi-Goutières syndromeYael Hacohen, Sameer Zuberi, Angela Vincent, et al.
Pageof 24