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Sandeep Jayawant

Showing results (11-20 of 50) with videos related to

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Neurology|August 23, 2015
Salbutamol and ephedrine in the treatment of severe AChR deficiency syndromesPedro M Rodríguez Cruz, Jacqueline Palace, Hayley Ramjattan, et al.
Archives of Disease in Childhood|September 13, 2011
Electroclinical outcome of children referred with suspected absence seizuresGeetha Anand, Anuruddha Padeniya, Rakesh Jain, et al.
Neuromuscular Disorders : NMD|September 24, 2011
Clinical features in a series of fast channel congenital myasthenia syndromeJacqueline Palace, Daniel Lashley, Stephen Bailey, et al.
Archives of Disease in Childhood|October 8, 2011
Video EEG outcome on children referred following a single unprovoked afebrile seizureGeetha Anand, Anuruddha Padeniya, Rakesh Jain, et al.
Neuromuscular Disorders : NMD|August 17, 2014
Congenital myopathies with secondary neuromuscular transmission defects; a case report and review of the literaturePedro M Rodríguez Cruz, Caroline Sewry, David Beeson, et al.
Developmental Medicine and Child Neurology|October 23, 2010
Alexander disease with periventricular calcification: a novel mutation of the GFAP geneRosalind J Jefferson, Michael Absoud, Rakesh Jain, et al.
Archives of Disease in Childhood|July 16, 2020
Disability and visual outcomes following suspected abusive head trauma in children under 2 yearsJuliana Wright, Sally Painter, Sheethal Sujayeendra Kodagali, et al.
Developmental Medicine and Child Neurology|November 22, 2011
Early use of high-dose riboflavin in a case of Brown-Vialetto-Van Laere syndromeGeetha Anand, Nadeem Hasan, Sathiya Jayapal, et al.
Developmental Medicine and Child Neurology|May 25, 2010
X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episodeGeetha Anand, Nitin Maheshwari, David Roberts, et al.
Brain : a Journal of Neurology|April 25, 2007
Clinical features of the DOK7 neuromuscular junction synaptopathyJacqueline Palace, Daniel Lashley, John Newsom-Davis, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Neurology|August 23, 2015
Salbutamol and ephedrine in the treatment of severe AChR deficiency syndromesPedro M Rodríguez Cruz, Jacqueline Palace, Hayley Ramjattan, et al.
Archives of Disease in Childhood|September 13, 2011
Electroclinical outcome of children referred with suspected absence seizuresGeetha Anand, Anuruddha Padeniya, Rakesh Jain, et al.
Neuromuscular Disorders : NMD|September 24, 2011
Clinical features in a series of fast channel congenital myasthenia syndromeJacqueline Palace, Daniel Lashley, Stephen Bailey, et al.
Archives of Disease in Childhood|October 8, 2011
Video EEG outcome on children referred following a single unprovoked afebrile seizureGeetha Anand, Anuruddha Padeniya, Rakesh Jain, et al.
Neuromuscular Disorders : NMD|August 17, 2014
Congenital myopathies with secondary neuromuscular transmission defects; a case report and review of the literaturePedro M Rodríguez Cruz, Caroline Sewry, David Beeson, et al.
Developmental Medicine and Child Neurology|October 23, 2010
Alexander disease with periventricular calcification: a novel mutation of the GFAP geneRosalind J Jefferson, Michael Absoud, Rakesh Jain, et al.
Archives of Disease in Childhood|July 16, 2020
Disability and visual outcomes following suspected abusive head trauma in children under 2 yearsJuliana Wright, Sally Painter, Sheethal Sujayeendra Kodagali, et al.
Developmental Medicine and Child Neurology|November 22, 2011
Early use of high-dose riboflavin in a case of Brown-Vialetto-Van Laere syndromeGeetha Anand, Nadeem Hasan, Sathiya Jayapal, et al.
Developmental Medicine and Child Neurology|May 25, 2010
X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episodeGeetha Anand, Nitin Maheshwari, David Roberts, et al.
Brain : a Journal of Neurology|April 25, 2007
Clinical features of the DOK7 neuromuscular junction synaptopathyJacqueline Palace, Daniel Lashley, John Newsom-Davis, et al.
Pageof 5