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Sithara Ramdas

Showing results (31-40 of 49) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 14, 2022
Rituximab in juvenile myasthenia gravis-an international cohort study and literature reviewSithara Ramdas, Adela Della Marina, Monique M Ryan, et al.
Neuromuscular Disorders : NMD|September 21, 2022
SARS-CoV-2 vaccination and new-onset myasthenia gravis: A report of 7 cases and review of the literatureSithara Ramdas, Ryan Malcolm Hum, Abigail Price, et al.
Neuromuscular Disorders : NMD|November 30, 2020
Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporterPedro M Rodríguez Cruz, Imelda Hughes, Adnan Manzur, et al.
Neuromuscular Disorders : NMD|December 15, 2022
Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature reviewSaraswathy Sabanathan, Deepti Gulhane, Kshitij Mankad, et al.
Neuromuscular Disorders : NMD|February 1, 2020
Paediatric myasthenia gravis: Prognostic factors for drug free remissionDomizia Vecchio, Sithara Ramdas, Pinki Munot, et al.
Multiple Sclerosis and Related Disorders|August 16, 2024
Study of seasonality of attacks in MOG antibody-associated diseaseAnna Francis, Monica Santos, Miguel Leal Rato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 29, 2021
Early predictors of disability of paediatric-onset AQP4-IgG-seropositive neuromyelitis optica spectrum disordersValentina Camera, Silvia Messina, Kariem Tarek Elhadd, et al.
Neurology|December 12, 2024
Quantitative Contribution of Clinical Attacks to Residual Disability in Patients With AQP4-Antibody Neuromyelitis Optica Spectrum DisorderBo Chen, Anna Francis, Sarah A Cooper, et al.
Brain : a Journal of Neurology|February 4, 2026
Optimal strategies for treatment discontinuation in MOG antibody-associated diseaseWei Z Yeh, Anna Francis, Sarah Cooper, et al.
Brain : a Journal of Neurology|February 3, 2026
Congenital myasthenic syndrome: is it time for a name change to genetic myasthenic syndrome?Sithara Ramdas, Yin Yao Dong, Pinki Munot, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 14, 2022
Rituximab in juvenile myasthenia gravis-an international cohort study and literature reviewSithara Ramdas, Adela Della Marina, Monique M Ryan, et al.
Neuromuscular Disorders : NMD|September 21, 2022
SARS-CoV-2 vaccination and new-onset myasthenia gravis: A report of 7 cases and review of the literatureSithara Ramdas, Ryan Malcolm Hum, Abigail Price, et al.
Neuromuscular Disorders : NMD|November 30, 2020
Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporterPedro M Rodríguez Cruz, Imelda Hughes, Adnan Manzur, et al.
Neuromuscular Disorders : NMD|December 15, 2022
Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature reviewSaraswathy Sabanathan, Deepti Gulhane, Kshitij Mankad, et al.
Neuromuscular Disorders : NMD|February 1, 2020
Paediatric myasthenia gravis: Prognostic factors for drug free remissionDomizia Vecchio, Sithara Ramdas, Pinki Munot, et al.
Multiple Sclerosis and Related Disorders|August 16, 2024
Study of seasonality of attacks in MOG antibody-associated diseaseAnna Francis, Monica Santos, Miguel Leal Rato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 29, 2021
Early predictors of disability of paediatric-onset AQP4-IgG-seropositive neuromyelitis optica spectrum disordersValentina Camera, Silvia Messina, Kariem Tarek Elhadd, et al.
Neurology|December 12, 2024
Quantitative Contribution of Clinical Attacks to Residual Disability in Patients With AQP4-Antibody Neuromyelitis Optica Spectrum DisorderBo Chen, Anna Francis, Sarah A Cooper, et al.
Brain : a Journal of Neurology|February 4, 2026
Optimal strategies for treatment discontinuation in MOG antibody-associated diseaseWei Z Yeh, Anna Francis, Sarah Cooper, et al.
Brain : a Journal of Neurology|February 3, 2026
Congenital myasthenic syndrome: is it time for a name change to genetic myasthenic syndrome?Sithara Ramdas, Yin Yao Dong, Pinki Munot, et al.
Pageof 5