Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sandeep Jayawant

Showing results (1-10 of 50) with videos related to

Pageof 5
Sort By:
Archives of Disease in Childhood|March 23, 2007
Outcome following subdural haemorrhages in infancySandeep Jayawant, Jeremy Parr
Indian Pediatrics|August 7, 2004
Congenital myotonic dystrophy: a rare cause of polyhydramniosSandeep Jayawant, Rajiv Sinha
Autoimmune Diseases|November 24, 2011
Juvenile myasthenia gravis: a paediatric perspectiveMaria F Finnis, Sandeep Jayawant
Neuromuscular Disorders : NMD|March 23, 2010
WITHDRAWN: Nemaline myopathy presenting as a stiff babyRakesh Kumar Jain, Sandeep Jayawant
Handbook of Clinical Neurology|April 30, 2013
Autoimmune myasthenia gravisSandeep Jayawant, Jeremy Parr, Angela Vincent
Archives of Disease in Childhood. Education and Practice Edition|June 24, 2011
It is all in the history, or is it?Geetha Anand, Sandeep Jayawant, Tony McShane, et al.
International Journal of Pediatric Otorhinolaryngology|September 14, 2016
Symptomatic stroke complicating central skull base osteomyelitis following otitis media in a 2-year old boy: Case report and review of the literatureEliz Kilich, Reena Dwivedi, Shelley Segal, 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.
Developmental Medicine and Child Neurology|September 15, 2009
A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorderMichael Absoud, Jeremy R Parr, Dorothy Halliday, et al.
Archives of Disease in Childhood|February 7, 2014
How common is childhood myasthenia? The UK incidence and prevalence of autoimmune and congenital myastheniaJeremy Ross Parr, Morag Jane Andrew, Maria Finnis, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Archives of Disease in Childhood|March 23, 2007
Outcome following subdural haemorrhages in infancySandeep Jayawant, Jeremy Parr
Indian Pediatrics|August 7, 2004
Congenital myotonic dystrophy: a rare cause of polyhydramniosSandeep Jayawant, Rajiv Sinha
Autoimmune Diseases|November 24, 2011
Juvenile myasthenia gravis: a paediatric perspectiveMaria F Finnis, Sandeep Jayawant
Neuromuscular Disorders : NMD|March 23, 2010
WITHDRAWN: Nemaline myopathy presenting as a stiff babyRakesh Kumar Jain, Sandeep Jayawant
Handbook of Clinical Neurology|April 30, 2013
Autoimmune myasthenia gravisSandeep Jayawant, Jeremy Parr, Angela Vincent
Archives of Disease in Childhood. Education and Practice Edition|June 24, 2011
It is all in the history, or is it?Geetha Anand, Sandeep Jayawant, Tony McShane, et al.
International Journal of Pediatric Otorhinolaryngology|September 14, 2016
Symptomatic stroke complicating central skull base osteomyelitis following otitis media in a 2-year old boy: Case report and review of the literatureEliz Kilich, Reena Dwivedi, Shelley Segal, 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.
Developmental Medicine and Child Neurology|September 15, 2009
A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorderMichael Absoud, Jeremy R Parr, Dorothy Halliday, et al.
Archives of Disease in Childhood|February 7, 2014
How common is childhood myasthenia? The UK incidence and prevalence of autoimmune and congenital myastheniaJeremy Ross Parr, Morag Jane Andrew, Maria Finnis, et al.
Pageof 5