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Sithara Ramdas

Showing results (11-20 of 49) with videos related to

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Expert Opinion on Investigational Drugs|March 22, 2022
Risdiplam: an investigational survival motor neuron 2 (SMN2) splicing modifier for spinal muscular atrophy (SMA)Theodora Markati, Gemma Fisher, Sithara Ramdas, et al.
BMJ Case Reports|October 6, 2016
Acute onset blindness: a case of optic neuritis and review of childhood optic neuritisSithara Ramdas, Danny Morrison, Michael Absoud, et al.
Neuromuscular Disorders : NMD|September 4, 2025
An observational longitudinal study of congenital myasthenic syndromesHayley Ramjattan, Leighann Henehan, Sithara Ramdas, et al.
European Journal of Pediatrics|July 2, 2013
Retinal haemorrhage in an infant following an accidental fall--a case reportSithara Ramdas, Una O'Colmain, N D L George, et al.
Archives of Disease in Childhood. Education and Practice Edition|January 8, 2025
Neonatal encephalopathy: when the diagnosis is not hypoxic ischaemic encephalopathyJacob Christopher Sutton Reading, Martin Smith, Robin Joseph, et al.
Journal of Neuromuscular Diseases|June 14, 2021
COVID-19 in a Cohort of Patients with Congenital Myasthenic SyndromeSetareh Alabaf, Karen O'Connell, Sithara Ramdas, et al.
The Turkish Journal of Pediatrics|July 3, 2023
Expanding the phenotype of DYNC1H1-associated diseases with a rare variant resulting in spinal muscular atrophy with lower extremity predominance (SMA-LED) and upper motor neuron signsJessica Lee, Philip Millington, Kavinda Dayasiri, et al.
Muscle & Nerve|June 6, 2022
Pregnancy outcomes in patients with congenital myasthenic syndromesKaren O'Connell, Tatiana Rooney, Setareh Alabaf, et al.
Biomedicines|November 27, 2024
Assessing the Utility of ColabFold and AlphaMissense in Determining Missense Variant Pathogenicity for Congenital Myasthenic SyndromesFinlay Ryan-Phillips, Leighann Henehan, Sithara Ramdas, et al.
Paediatric Drugs|August 28, 2024
Targeted Treatments for Myasthenia Gravis in Children and AdolescentsSithara Ramdas, Teresa Painho, Maria I Vanegas, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Expert Opinion on Investigational Drugs|March 22, 2022
Risdiplam: an investigational survival motor neuron 2 (SMN2) splicing modifier for spinal muscular atrophy (SMA)Theodora Markati, Gemma Fisher, Sithara Ramdas, et al.
BMJ Case Reports|October 6, 2016
Acute onset blindness: a case of optic neuritis and review of childhood optic neuritisSithara Ramdas, Danny Morrison, Michael Absoud, et al.
Neuromuscular Disorders : NMD|September 4, 2025
An observational longitudinal study of congenital myasthenic syndromesHayley Ramjattan, Leighann Henehan, Sithara Ramdas, et al.
European Journal of Pediatrics|July 2, 2013
Retinal haemorrhage in an infant following an accidental fall--a case reportSithara Ramdas, Una O'Colmain, N D L George, et al.
Archives of Disease in Childhood. Education and Practice Edition|January 8, 2025
Neonatal encephalopathy: when the diagnosis is not hypoxic ischaemic encephalopathyJacob Christopher Sutton Reading, Martin Smith, Robin Joseph, et al.
Journal of Neuromuscular Diseases|June 14, 2021
COVID-19 in a Cohort of Patients with Congenital Myasthenic SyndromeSetareh Alabaf, Karen O'Connell, Sithara Ramdas, et al.
The Turkish Journal of Pediatrics|July 3, 2023
Expanding the phenotype of DYNC1H1-associated diseases with a rare variant resulting in spinal muscular atrophy with lower extremity predominance (SMA-LED) and upper motor neuron signsJessica Lee, Philip Millington, Kavinda Dayasiri, et al.
Muscle & Nerve|June 6, 2022
Pregnancy outcomes in patients with congenital myasthenic syndromesKaren O'Connell, Tatiana Rooney, Setareh Alabaf, et al.
Biomedicines|November 27, 2024
Assessing the Utility of ColabFold and AlphaMissense in Determining Missense Variant Pathogenicity for Congenital Myasthenic SyndromesFinlay Ryan-Phillips, Leighann Henehan, Sithara Ramdas, et al.
Paediatric Drugs|August 28, 2024
Targeted Treatments for Myasthenia Gravis in Children and AdolescentsSithara Ramdas, Teresa Painho, Maria I Vanegas, et al.
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