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

H Sueoka

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
No to Hattatsu = Brain and Development|November 30, 1999
[Seizure exacerbation by the use of leuprorelin acetate for treatment of central precocious puberty in a female patient with symptomatic localization-related epilepsy]K Minagawa, H Sueoka
Genetic Testing|January 6, 2001
Rapid mutation screening of phenylketonuria by polymerase chain reaction-linked restriction enzyme assay and direct sequence of the phenylalanine hydroxylase gene: clinical application in northern Japan and northern ChinaH Sueoka, M Nagao, S Chiba
Journal of Pediatric Surgery|June 1, 1985
Clinical and histologic studies of neuronal intestinal dysplasiaK Munakata, K Morita, I Okabe, et al.
Journal of Human Genetics|November 26, 1999
Mutation screening of phenylketonuria in the Far East of RussiaH Sueoka, A Moshinetsky, M Nagao, et al.
European Journal of Pediatrics|August 1, 1996
Severe myoclonic epilepsy in infancy and carbamazepineS Wakai, N Ito, H Sueoka, et al.
Pediatric Neurology|September 1, 1995
Complex partial status epilepticus in childhoodS Wakai, N Ito, H Sueoka, et al.
Epilepsia|October 1, 1996
"Obtundation status (Dravet)" caused by complex partial status epilepticus in a patient with severe myoclonic epilepsy in infancyS Wakai, M Ikehata, H Nihira, et al.
Lancet (London, England)|November 12, 1994
Classification of familial neonatal convulsionsS Wakai, H Kamasaki, N Itoh, et al.
Epilepsia|July 1, 1994
Ictal video-EEG analysis of infantile neuroaxonal dystrophyS Wakai, H Asanuma, H Hayasaka, et al.
New Microbes and New Infections|July 1, 2017
Septic arthritis caused by an emerging ST121 methicillin-susceptible, PVL-negative <i>Staphylococcus aureus</i> harbouring a variant of bone sialoprotein-binding protein geneA Togashi, M S Aung, Y Yoto, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
No to Hattatsu = Brain and Development|November 30, 1999
[Seizure exacerbation by the use of leuprorelin acetate for treatment of central precocious puberty in a female patient with symptomatic localization-related epilepsy]K Minagawa, H Sueoka
Genetic Testing|January 6, 2001
Rapid mutation screening of phenylketonuria by polymerase chain reaction-linked restriction enzyme assay and direct sequence of the phenylalanine hydroxylase gene: clinical application in northern Japan and northern ChinaH Sueoka, M Nagao, S Chiba
Journal of Pediatric Surgery|June 1, 1985
Clinical and histologic studies of neuronal intestinal dysplasiaK Munakata, K Morita, I Okabe, et al.
Journal of Human Genetics|November 26, 1999
Mutation screening of phenylketonuria in the Far East of RussiaH Sueoka, A Moshinetsky, M Nagao, et al.
European Journal of Pediatrics|August 1, 1996
Severe myoclonic epilepsy in infancy and carbamazepineS Wakai, N Ito, H Sueoka, et al.
Pediatric Neurology|September 1, 1995
Complex partial status epilepticus in childhoodS Wakai, N Ito, H Sueoka, et al.
Epilepsia|October 1, 1996
"Obtundation status (Dravet)" caused by complex partial status epilepticus in a patient with severe myoclonic epilepsy in infancyS Wakai, M Ikehata, H Nihira, et al.
Lancet (London, England)|November 12, 1994
Classification of familial neonatal convulsionsS Wakai, H Kamasaki, N Itoh, et al.
Epilepsia|July 1, 1994
Ictal video-EEG analysis of infantile neuroaxonal dystrophyS Wakai, H Asanuma, H Hayasaka, et al.
New Microbes and New Infections|July 1, 2017
Septic arthritis caused by an emerging ST121 methicillin-susceptible, PVL-negative <i>Staphylococcus aureus</i> harbouring a variant of bone sialoprotein-binding protein geneA Togashi, M S Aung, Y Yoto, et al.
Pageof 2