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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.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. Genes 2022, 13, 2110Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, 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.Brain & Development|December 30, 2011
Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patientsTomoko Mizuno, Hirofumi Komaki, Masayuki Sasaki, et al.Orphanet Journal of Rare Diseases|July 8, 2021
Cybernic treatment with wearable cyborg Hybrid Assistive Limb (HAL) improves ambulatory function in patients with slowly progressive rare neuromuscular diseases: a multicentre, randomised, controlled crossover trial for efficacy and safety (NCY-3001)Takashi Nakajima, Yoshiyuki Sankai, Shinjiro Takata, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 18, 2012
Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2BToshiaki Takahashi, Masashi Aoki, Naoki Suzuki, et al.Pageof 10