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American Journal of Medical Genetics. Part A
|
October 29, 2024
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, et al.
Movement Disorders Clinical Practice
|
October 17, 2022
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children
Divyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.
Pediatrics
|
November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus Guidelines
Terrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
July 24, 2021
International Consensus Recommendations for the Treatment of Pediatric NMDAR Antibody Encephalitis
Margherita Nosadini, Terrence Thomas, Michael Eyre, et al.
JAMA Neurology
|
September 20, 2021
Use and Safety of Immunotherapeutic Management of N-Methyl-d-Aspartate Receptor Antibody Encephalitis: A Meta-analysis
Margherita Nosadini, Michael Eyre, Erika Molteni, et al.
BMJ Open
|
April 3, 2025
Effectiveness and safety of shortened intensive treatment for children with tuberculous meningitis (SURE): a protocol for a phase 3 randomised controlled trial evaluating 6 months of antituberculosis therapy and 8 weeks of aspirin in Asian and African children with tuberculous meningitis
Julie Huynh, Chishala Chabala, Suvasini Sharma, et al.
Clinical Genetics
|
July 24, 2021
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities
Parneet Kaur, Michelle C do Rosario, Malavika Hebbar, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India
Shruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics
|
February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications
Purvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
Epilepsia
|
March 14, 2020
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases
Felippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, et al.
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of 20
Search research articles
Search
Showing results (181-190 of 196) with videos related to
Sort By:
Page
of 20
American Journal of Medical Genetics. Part A
|
October 29, 2024
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, et al.
Movement Disorders Clinical Practice
|
October 17, 2022
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children
Divyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.
Pediatrics
|
November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus Guidelines
Terrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
July 24, 2021
International Consensus Recommendations for the Treatment of Pediatric NMDAR Antibody Encephalitis
Margherita Nosadini, Terrence Thomas, Michael Eyre, et al.
JAMA Neurology
|
September 20, 2021
Use and Safety of Immunotherapeutic Management of N-Methyl-d-Aspartate Receptor Antibody Encephalitis: A Meta-analysis
Margherita Nosadini, Michael Eyre, Erika Molteni, et al.
BMJ Open
|
April 3, 2025
Effectiveness and safety of shortened intensive treatment for children with tuberculous meningitis (SURE): a protocol for a phase 3 randomised controlled trial evaluating 6 months of antituberculosis therapy and 8 weeks of aspirin in Asian and African children with tuberculous meningitis
Julie Huynh, Chishala Chabala, Suvasini Sharma, et al.
Clinical Genetics
|
July 24, 2021
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities
Parneet Kaur, Michelle C do Rosario, Malavika Hebbar, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India
Shruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics
|
February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications
Purvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
Epilepsia
|
March 14, 2020
KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases
Felippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, et al.
Page
of 20