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Ming J Lim

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Developmental Medicine and Child Neurology|July 17, 2024
UK research priority setting for childhood neurological conditionsJill Cadwgan, Jane Goodwin, Barbara Babcock, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2023
Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease courseOmar Abdel-Mannan, Dimitrios Champsas, Carmen Tur, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 2012
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigensYael Hacohen, Sukhvir Wright, Patrick Waters, et al.
Pediatrics|March 25, 2015
Infectious and autoantibody-associated encephalitis: clinical features and long-term outcomeSekhar C Pillai, Yael Hacohen, Esther Tantsis, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Brain : a Journal of Neurology|February 5, 2010
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorderWilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, et al.
American Journal of Human Genetics|September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndromeGillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Developmental Medicine and Child Neurology|July 17, 2024
UK research priority setting for childhood neurological conditionsJill Cadwgan, Jane Goodwin, Barbara Babcock, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2023
Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease courseOmar Abdel-Mannan, Dimitrios Champsas, Carmen Tur, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 2012
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigensYael Hacohen, Sukhvir Wright, Patrick Waters, et al.
Pediatrics|March 25, 2015
Infectious and autoantibody-associated encephalitis: clinical features and long-term outcomeSekhar C Pillai, Yael Hacohen, Esther Tantsis, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Brain : a Journal of Neurology|February 5, 2010
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorderWilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, et al.
American Journal of Human Genetics|September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndromeGillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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