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Hiroyuki Awano

Showing results (141-150 of 152) with videos related to

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Brain & Development|May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNAMawaddah Ar Rochmah, Nur Imma Fatimah Harahap, Emma Tabe Eko Niba, et al.
Nature Materials|December 5, 2018
Long spin coherence length and bulk-like spin-orbit torque in ferrimagnetic multilayersJiawei Yu, Do Bang, Rahul Mishra, et al.
The Kobe Journal of Medical Sciences|August 21, 2020
Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 PatientsMawaddah Ar Rochmah, Yogik Onky Silvana Wijaya, Nur Imma Fatimah Harahap, et al.
Neuropsychopharmacology Reports|August 15, 2025
Nonrandomized Allocation of Steroid Therapy in Patients With Fukuyama Congenital Muscular Dystrophy: Study Protocol for a Phase II Clinical TrialTerumi Murakami, Takatoshi Sato, Takami Ishizuka, et al.
Journal of Neurology|July 16, 2025
Charcot-Marie-Tooth-like presentation in giant axonal neuropathy: clinical variability and prevalence in a large Japanese case seriesTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Genes|November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, JapanYoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Genes|March 29, 2023
Correction: Noguchi et al. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. <i>Genes</i> 2022, <i>13</i>, 2110Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
International Journal of Neonatal Screening|July 21, 2021
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in JapanTomokazu Kimizu, Shinobu Ida, Kentaro Okamoto, et al.
JAMA Neurology|April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 AutoantibodiesMichio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Brain & Development|April 24, 2021
Phenotypes of SMA patients retaining SMN1 with intragenic mutationYogik Onky Silvana Wijaya, Mawaddah Ar Rohmah, Emma Tabe Eko Niba, et al.
Pageof 16

Showing results (141-150 of 152) with videos related to

Sort By:
Pageof 16
Brain & Development|May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNAMawaddah Ar Rochmah, Nur Imma Fatimah Harahap, Emma Tabe Eko Niba, et al.
Nature Materials|December 5, 2018
Long spin coherence length and bulk-like spin-orbit torque in ferrimagnetic multilayersJiawei Yu, Do Bang, Rahul Mishra, et al.
The Kobe Journal of Medical Sciences|August 21, 2020
Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 PatientsMawaddah Ar Rochmah, Yogik Onky Silvana Wijaya, Nur Imma Fatimah Harahap, et al.
Neuropsychopharmacology Reports|August 15, 2025
Nonrandomized Allocation of Steroid Therapy in Patients With Fukuyama Congenital Muscular Dystrophy: Study Protocol for a Phase II Clinical TrialTerumi Murakami, Takatoshi Sato, Takami Ishizuka, et al.
Journal of Neurology|July 16, 2025
Charcot-Marie-Tooth-like presentation in giant axonal neuropathy: clinical variability and prevalence in a large Japanese case seriesTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Genes|November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, JapanYoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Genes|March 29, 2023
Correction: Noguchi et al. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. <i>Genes</i> 2022, <i>13</i>, 2110Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
International Journal of Neonatal Screening|July 21, 2021
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in JapanTomokazu Kimizu, Shinobu Ida, Kentaro Okamoto, et al.
JAMA Neurology|April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 AutoantibodiesMichio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Brain & Development|April 24, 2021
Phenotypes of SMA patients retaining SMN1 with intragenic mutationYogik Onky Silvana Wijaya, Mawaddah Ar Rohmah, Emma Tabe Eko Niba, et al.
Pageof 16