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Tetsuya Okazaki

Showing results (41-50 of 51) with videos related to

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Yonago Acta Medica|April 10, 2019
Recurrent Erythema Nodosum in a Child with a <i>SHOC2</i> Gene MutationTetsuya Okazaki, Yoshiaki Saito, Kazunari Sugita, et al.
Brain & Development|December 28, 2013
Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgeryYukari Endo, Yoshiaki Saito, Taisuke Otsuki, et al.
Brain : a Journal of Neurology|February 5, 2019
Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophyMasayuki Itoh, Hongmei Dai, Shin-Ichi Horike, et al.
Epilepsia Open|June 7, 2021
Efficacy of long-term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case seriesShimpei Baba, Tohru Okanishi, Yoichiro Homma, et al.
Journal of Leukocyte Biology|December 18, 2013
Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasisYoko Mizoguchi, Miyuki Tsumura, Satoshi Okada, et al.
Artificial Organs|September 18, 2024
The polymyxin-B direct hemoperfusion OPTimal Initiation timing with Catecholamine PMX-OPTIC study: A multicenter retrospective observational studyKensuke Nakamura, Tetsuya Okazaki, Akihito Tampo, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 10, 2020
Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13Nobuhiro Suzumori, Akihiko Sekizawa, Eri Takeda, et al.
American Journal of Human Genetics|November 26, 2018
MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon GuidanceWilliam B Dobyns, Kimberly A Aldinger, Gisele E Ishak, et al.
Journal of Medical Genetics|March 8, 2019
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencingKazuhiro Iwama, Takeshi Mizuguchi, Eri Takeshita, et al.
Human Mutation|November 1, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analysesYuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Yonago Acta Medica|April 10, 2019
Recurrent Erythema Nodosum in a Child with a <i>SHOC2</i> Gene MutationTetsuya Okazaki, Yoshiaki Saito, Kazunari Sugita, et al.
Brain & Development|December 28, 2013
Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgeryYukari Endo, Yoshiaki Saito, Taisuke Otsuki, et al.
Brain : a Journal of Neurology|February 5, 2019
Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophyMasayuki Itoh, Hongmei Dai, Shin-Ichi Horike, et al.
Epilepsia Open|June 7, 2021
Efficacy of long-term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case seriesShimpei Baba, Tohru Okanishi, Yoichiro Homma, et al.
Journal of Leukocyte Biology|December 18, 2013
Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasisYoko Mizoguchi, Miyuki Tsumura, Satoshi Okada, et al.
Artificial Organs|September 18, 2024
The polymyxin-B direct hemoperfusion OPTimal Initiation timing with Catecholamine PMX-OPTIC study: A multicenter retrospective observational studyKensuke Nakamura, Tetsuya Okazaki, Akihito Tampo, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 10, 2020
Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13Nobuhiro Suzumori, Akihiko Sekizawa, Eri Takeda, et al.
American Journal of Human Genetics|November 26, 2018
MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon GuidanceWilliam B Dobyns, Kimberly A Aldinger, Gisele E Ishak, et al.
Journal of Medical Genetics|March 8, 2019
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencingKazuhiro Iwama, Takeshi Mizuguchi, Eri Takeshita, et al.
Human Mutation|November 1, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analysesYuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, et al.
Pageof 6