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Hidehito Kondo

Showing results (11-20 of 16) with videos related to

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Legal Medicine (Tokyo, Japan)|December 28, 2023
Fatal cardiac dysfunction in a child with Williams syndromeChihiro Kawai, Hidehito Kondo, Masashi Miyao, et al.
Journal of the Endocrine Society|May 7, 2020
Endocrinological Features of Hartsfield Syndrome in an Adult Patient With a Novel Mutation of <i>FGFR1</i>Sachiko Kobayashi, Junpei Tanigawa, Hidehito Kondo, et al.
Brain & Development|February 11, 2023
Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deletion of SCN1AHiroaki Hanafusa, Hiroshi Yamaguchi, Hidehito Kondo, et al.
Human Molecular Genetics|December 26, 2016
Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptomsHidehito Kondo, Nadezda Maksimova, Takanobu Otomo, et al.
Journal of Medical Case Reports|February 13, 2022
Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case seriesYoshinori Satomura, Kazuhiko Bessho, Nobutoshi Nawa, et al.
Frontiers in Neuroscience|March 16, 2023
Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2Hiroshi Sakuma, Jun-Ichi Takanashi, Kazuhiro Muramatsu, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Legal Medicine (Tokyo, Japan)|December 28, 2023
Fatal cardiac dysfunction in a child with Williams syndromeChihiro Kawai, Hidehito Kondo, Masashi Miyao, et al.
Journal of the Endocrine Society|May 7, 2020
Endocrinological Features of Hartsfield Syndrome in an Adult Patient With a Novel Mutation of <i>FGFR1</i>Sachiko Kobayashi, Junpei Tanigawa, Hidehito Kondo, et al.
Brain & Development|February 11, 2023
Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deletion of SCN1AHiroaki Hanafusa, Hiroshi Yamaguchi, Hidehito Kondo, et al.
Human Molecular Genetics|December 26, 2016
Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptomsHidehito Kondo, Nadezda Maksimova, Takanobu Otomo, et al.
Journal of Medical Case Reports|February 13, 2022
Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case seriesYoshinori Satomura, Kazuhiko Bessho, Nobutoshi Nawa, et al.
Frontiers in Neuroscience|March 16, 2023
Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2Hiroshi Sakuma, Jun-Ichi Takanashi, Kazuhiro Muramatsu, et al.
Pageof 2