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Brain & Development
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May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA
Mawaddah 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 multilayers
Jiawei 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 Patients
Mawaddah 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 Trial
Terumi 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 series
Takahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Genes
|
November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
Yoriko 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>, 2110
Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
International Journal of Neonatal Screening
|
July 21, 2021
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan
Tomokazu Kimizu, Shinobu Ida, Kentaro Okamoto, et al.
JAMA Neurology
|
April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 Autoantibodies
Michio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Brain & Development
|
April 24, 2021
Phenotypes of SMA patients retaining SMN1 with intragenic mutation
Yogik Onky Silvana Wijaya, Mawaddah Ar Rohmah, Emma Tabe Eko Niba, et al.
Page
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Search research articles
Search
Showing results (141-150 of 152) with videos related to
Sort By:
Page
of 16
Brain & Development
|
May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA
Mawaddah 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 multilayers
Jiawei 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 Patients
Mawaddah 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 Trial
Terumi 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 series
Takahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Genes
|
November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
Yoriko 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>, 2110
Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
International Journal of Neonatal Screening
|
July 21, 2021
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan
Tomokazu Kimizu, Shinobu Ida, Kentaro Okamoto, et al.
JAMA Neurology
|
April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 Autoantibodies
Michio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Brain & Development
|
April 24, 2021
Phenotypes of SMA patients retaining SMN1 with intragenic mutation
Yogik Onky Silvana Wijaya, Mawaddah Ar Rohmah, Emma Tabe Eko Niba, et al.
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of 16