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

Sheffali Gulati

Showing results (181-190 of 368) with videos related to

Pageof 37
Sort By:
Annals of Indian Academy of Neurology|December 16, 2014
Candida tropicalis brain abscess in a neonate: An emerging nosocomial menaceSangeetha Yoganathan, Biswaroop Chakrabarty, Sheffali Gulati, et al.
Indian Journal of Pediatrics|June 16, 2012
Macrocephaly with diffuse white matter changes simulating a leukodystrophy in Menkes diseasePuneet Jain, Suvasini Sharma, Naveen Sankhyan, et al.
Neurology India|January 4, 2024
Novel <i>SLC16A2</i> Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan-Herndon-Dudley SyndromeAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Indian Journal of Pediatrics|March 27, 2024
Prevalence of Sensory Processing Deficits in Children with Spastic Cerebral Palsy - An Indian Caregiver's PerspectiveSapna Dhiman, Ramesh K Goyal, Aakash Mahesan, et al.
European Child & Adolescent Psychiatry|August 28, 2021
Correction to: Response (minimum clinically relevant change) in ASD symptoms after an intervention according to CARS-2: consensus from an expert elicitation procedureLucie Jurek, Matias Baltazar, Sheffali Gulati, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian originRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Pediatric Blood & Cancer|June 15, 2010
Acute onset flaccid quadriparesis in pediatric non-Hodgkin lymphoma: vincristine induced or Guillain-Barré syndrome?Ankur Bahl, Biswaroop Chakrabarty, Sheffali Gulati, et al.
Journal of Child Neurology|June 20, 2013
Vincristine-induced neuropathy in childhood ALL (acute lymphoblastic leukemia) survivors: prevalence and electrophysiological characteristicsPuneet Jain, Sheffali Gulati, Rachna Seth, et al.
Journal of Child Neurology|May 27, 2014
Serum alpha tocopherol, vitamin B12, and folate levels in childhood acute lymphoblastic leukemia survivors with and without neuropathyPuneet Jain, Sheffali Gulati, G S Toteja, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Pageof 37

Showing results (181-190 of 368) with videos related to

Sort By:
Pageof 37
Annals of Indian Academy of Neurology|December 16, 2014
Candida tropicalis brain abscess in a neonate: An emerging nosocomial menaceSangeetha Yoganathan, Biswaroop Chakrabarty, Sheffali Gulati, et al.
Indian Journal of Pediatrics|June 16, 2012
Macrocephaly with diffuse white matter changes simulating a leukodystrophy in Menkes diseasePuneet Jain, Suvasini Sharma, Naveen Sankhyan, et al.
Neurology India|January 4, 2024
Novel <i>SLC16A2</i> Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan-Herndon-Dudley SyndromeAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Indian Journal of Pediatrics|March 27, 2024
Prevalence of Sensory Processing Deficits in Children with Spastic Cerebral Palsy - An Indian Caregiver's PerspectiveSapna Dhiman, Ramesh K Goyal, Aakash Mahesan, et al.
European Child & Adolescent Psychiatry|August 28, 2021
Correction to: Response (minimum clinically relevant change) in ASD symptoms after an intervention according to CARS-2: consensus from an expert elicitation procedureLucie Jurek, Matias Baltazar, Sheffali Gulati, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian originRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Pediatric Blood & Cancer|June 15, 2010
Acute onset flaccid quadriparesis in pediatric non-Hodgkin lymphoma: vincristine induced or Guillain-Barré syndrome?Ankur Bahl, Biswaroop Chakrabarty, Sheffali Gulati, et al.
Journal of Child Neurology|June 20, 2013
Vincristine-induced neuropathy in childhood ALL (acute lymphoblastic leukemia) survivors: prevalence and electrophysiological characteristicsPuneet Jain, Sheffali Gulati, Rachna Seth, et al.
Journal of Child Neurology|May 27, 2014
Serum alpha tocopherol, vitamin B12, and folate levels in childhood acute lymphoblastic leukemia survivors with and without neuropathyPuneet Jain, Sheffali Gulati, G S Toteja, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Pageof 37