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

Gautam Ambegaonkar

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Archives of Disease in Childhood. Education and Practice Edition|September 24, 2017
Post-traumatic seizure with an unexpected findingChristine Brittain, Gautam Ambegaonkar
Archives of Disease in Childhood|September 27, 2007
To pee or not to peeGautam Ambegaonkar, Roopa Mulik
Archives of Disease in Childhood|November 11, 2016
Acute necrotising encephalopathy of childhood: an uncommon cause of childhood encephalopathy with recognisable clinical and radiological features and genetic predispositionNicholas Schindler, Gautam Ambegaonkar
BMJ Case Reports|November 1, 2016
Glycine receptor antibody-associated epilepsy in a boy aged 4 yearsChinwe Ude, Gautam Ambegaonkar
Archives of Disease in Childhood. Education and Practice Edition|December 10, 2017
Fifteen minute consultation: an approach to the child with chronic headachesNichola Aspinall, Anita D'Urso, Gautam Ambegaonkar
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2011
The multiple phenotypes of arthrogryposis multiplex congenita with reference to the neurogenic variantGautam Ambegaonkar, Adnan Y Manzur, Stephanie A Robb, et al.
Archives of Disease in Childhood. Education and Practice Edition|January 8, 2021
Fifteen-minute consultation: The efficient investigation of infantile and childhood epileptic encephalopathies in the era of modern genomicsLuke Daniel Perry, Sarah Louise Hogg, Sarah Bowdin, et al.
Developmental Medicine and Child Neurology|December 10, 2015
GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathyApostolos Papandreou, Amy McTague, Natalie Trump, et al.
Neurogenetics|January 8, 2017
Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected childKatherine Schon, Olivera Spasic-Boskovic, Kim Brugger, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great BritainNikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Archives of Disease in Childhood. Education and Practice Edition|September 24, 2017
Post-traumatic seizure with an unexpected findingChristine Brittain, Gautam Ambegaonkar
Archives of Disease in Childhood|September 27, 2007
To pee or not to peeGautam Ambegaonkar, Roopa Mulik
Archives of Disease in Childhood|November 11, 2016
Acute necrotising encephalopathy of childhood: an uncommon cause of childhood encephalopathy with recognisable clinical and radiological features and genetic predispositionNicholas Schindler, Gautam Ambegaonkar
BMJ Case Reports|November 1, 2016
Glycine receptor antibody-associated epilepsy in a boy aged 4 yearsChinwe Ude, Gautam Ambegaonkar
Archives of Disease in Childhood. Education and Practice Edition|December 10, 2017
Fifteen minute consultation: an approach to the child with chronic headachesNichola Aspinall, Anita D'Urso, Gautam Ambegaonkar
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2011
The multiple phenotypes of arthrogryposis multiplex congenita with reference to the neurogenic variantGautam Ambegaonkar, Adnan Y Manzur, Stephanie A Robb, et al.
Archives of Disease in Childhood. Education and Practice Edition|January 8, 2021
Fifteen-minute consultation: The efficient investigation of infantile and childhood epileptic encephalopathies in the era of modern genomicsLuke Daniel Perry, Sarah Louise Hogg, Sarah Bowdin, et al.
Developmental Medicine and Child Neurology|December 10, 2015
GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathyApostolos Papandreou, Amy McTague, Natalie Trump, et al.
Neurogenetics|January 8, 2017
Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected childKatherine Schon, Olivera Spasic-Boskovic, Kim Brugger, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great BritainNikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Pageof 2