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

Yusuke Takezawa

Showing results (41-50 of 53) with videos related to

Pageof 6
Sort By:
Dalton Transactions (Cambridge, England : 2003)|November 30, 2010
Incorporation of organometallic Ru complexes into apo-ferritin cageYusuke Takezawa, Philipp Böckmann, Naoki Sugi, et al.
Brain & Development|October 3, 2015
Outcome of hemiplegic cerebral palsy born at term depends on its etiologyYukihiro Kitai, Kazuhiro Haginoya, Satori Hirai, et al.
The Tohoku Journal of Experimental Medicine|July 6, 2022
Multiple Cerebral Hemorrhages and White Matter Lesions Developing after Severe hMPV Pneumonia in a Patient with Trisomy 13: A Case Report and Review of the LiteratureMoriei Shibuya, Noriko Togashi, Takehiko Inui, et al.
Journal of Human Genetics|February 3, 2017
A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndromeTakehiko Inui, Mai Anzai, Yusuke Takezawa, et al.
Brain & Development|May 29, 2017
A patient with Muenke syndrome manifesting migrating neonatal seizuresYukimune Okubo, Taro Kitamura, Mai Anzai, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Journal of the Neurological Sciences|March 6, 2016
FDG-PET study of patients with Leigh syndromeKauzhiro Haginoya, Tomohiro Kaneta, Noriko Togashi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Solitary median maxillary central incisor syndrome caused by 22q11.2 microdeletionHirohito Shima, Akinobu Miura, Sayaka Kawashima, et al.
Journal of Human Genetics|March 8, 2019
Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndromeSato Suzuki-Muromoto, Takuya Miyabayashi, Koki Nagai, et al.
Brain & Development|November 19, 2019
Phenotype-genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasmsWakaba Endo, Satoru Ikemoto, Noriko Togashi, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Dalton Transactions (Cambridge, England : 2003)|November 30, 2010
Incorporation of organometallic Ru complexes into apo-ferritin cageYusuke Takezawa, Philipp Böckmann, Naoki Sugi, et al.
Brain & Development|October 3, 2015
Outcome of hemiplegic cerebral palsy born at term depends on its etiologyYukihiro Kitai, Kazuhiro Haginoya, Satori Hirai, et al.
The Tohoku Journal of Experimental Medicine|July 6, 2022
Multiple Cerebral Hemorrhages and White Matter Lesions Developing after Severe hMPV Pneumonia in a Patient with Trisomy 13: A Case Report and Review of the LiteratureMoriei Shibuya, Noriko Togashi, Takehiko Inui, et al.
Journal of Human Genetics|February 3, 2017
A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndromeTakehiko Inui, Mai Anzai, Yusuke Takezawa, et al.
Brain & Development|May 29, 2017
A patient with Muenke syndrome manifesting migrating neonatal seizuresYukimune Okubo, Taro Kitamura, Mai Anzai, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Journal of the Neurological Sciences|March 6, 2016
FDG-PET study of patients with Leigh syndromeKauzhiro Haginoya, Tomohiro Kaneta, Noriko Togashi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Solitary median maxillary central incisor syndrome caused by 22q11.2 microdeletionHirohito Shima, Akinobu Miura, Sayaka Kawashima, et al.
Journal of Human Genetics|March 8, 2019
Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndromeSato Suzuki-Muromoto, Takuya Miyabayashi, Koki Nagai, et al.
Brain & Development|November 19, 2019
Phenotype-genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasmsWakaba Endo, Satoru Ikemoto, Noriko Togashi, et al.
Pageof 6