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James P Fryer

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

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Human Genetics|September 19, 2003
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotypeRichard A King, Jacy Pietsch, James P Fryer, et al.
Neurology|October 4, 2019
Autologous nonmyeloablative hematopoietic stem cell transplantation for neuromyelitis opticaRichard K Burt, Roumen Balabanov, Xiaoqiang Han, et al.
JAMA Ophthalmology|February 23, 2018
Prevalence of Myelin Oligodendrocyte Glycoprotein and Aquaporin-4-IgG in Patients in the Optic Neuritis Treatment TrialJohn J Chen, W Oliver Tobin, Masoud Majed, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 13, 2018
Autoimmune septin-5 cerebellar ataxiaJosephe A Honorat, A Sebastian Lopez-Chiriboga, Thomas J Kryzer, et al.
American Journal of Human Genetics|July 24, 2003
MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Richard A King, Rebecca K Willaert, Ramona M Schmidt, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 2011
Molecular outcomes of neuromyelitis optica (NMO)-IgG binding to aquaporin-4 in astrocytesShannon R Hinson, Michael F Romero, Bogdan F Gh Popescu, et al.
JAMA Network Open|April 21, 2025
Late Relapse After Autologous Hematopoietic Stem Cell Transplantation in AQP4-IgG-Positive NMOSDNisa Vorasoot, Kyle M Blackburn, Linda Nguyen, et al.
The Journal of Experimental Medicine|October 8, 2008
Aquaporin-4-binding autoantibodies in patients with neuromyelitis optica impair glutamate transport by down-regulating EAAT2Shannon R Hinson, Shanu F Roemer, Claudia F Lucchinetti, et al.
Archives of Neurology|September 16, 2009
Diagnosis of neuromyelitis spectrum disorders: comparative sensitivities and specificities of immunohistochemical and immunoprecipitation assaysAndrew McKeon, James P Fryer, Metha Apiwattanakul, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 8, 2019
Seroprevalence and clinical phenotype of MOG-IgG-associated disorders in Sri LankaBimsara Senanayake, Jiraporn Jitprapaikulsan, Mythily Aravinthan, et al.
Pageof 5

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

Sort By:
Pageof 5
Human Genetics|September 19, 2003
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotypeRichard A King, Jacy Pietsch, James P Fryer, et al.
Neurology|October 4, 2019
Autologous nonmyeloablative hematopoietic stem cell transplantation for neuromyelitis opticaRichard K Burt, Roumen Balabanov, Xiaoqiang Han, et al.
JAMA Ophthalmology|February 23, 2018
Prevalence of Myelin Oligodendrocyte Glycoprotein and Aquaporin-4-IgG in Patients in the Optic Neuritis Treatment TrialJohn J Chen, W Oliver Tobin, Masoud Majed, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 13, 2018
Autoimmune septin-5 cerebellar ataxiaJosephe A Honorat, A Sebastian Lopez-Chiriboga, Thomas J Kryzer, et al.
American Journal of Human Genetics|July 24, 2003
MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Richard A King, Rebecca K Willaert, Ramona M Schmidt, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 2011
Molecular outcomes of neuromyelitis optica (NMO)-IgG binding to aquaporin-4 in astrocytesShannon R Hinson, Michael F Romero, Bogdan F Gh Popescu, et al.
JAMA Network Open|April 21, 2025
Late Relapse After Autologous Hematopoietic Stem Cell Transplantation in AQP4-IgG-Positive NMOSDNisa Vorasoot, Kyle M Blackburn, Linda Nguyen, et al.
The Journal of Experimental Medicine|October 8, 2008
Aquaporin-4-binding autoantibodies in patients with neuromyelitis optica impair glutamate transport by down-regulating EAAT2Shannon R Hinson, Shanu F Roemer, Claudia F Lucchinetti, et al.
Archives of Neurology|September 16, 2009
Diagnosis of neuromyelitis spectrum disorders: comparative sensitivities and specificities of immunohistochemical and immunoprecipitation assaysAndrew McKeon, James P Fryer, Metha Apiwattanakul, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 8, 2019
Seroprevalence and clinical phenotype of MOG-IgG-associated disorders in Sri LankaBimsara Senanayake, Jiraporn Jitprapaikulsan, Mythily Aravinthan, et al.
Pageof 5