National Hospital Organization Higashisaitama National Hospital

Alternate names: Higashisaitama National Hospital, National Higashisaitama Hospital, 国立病院機構東埼玉病院, 東埼玉病院

Parent institution: National Hospital Organization

ROR: 040vrc517

OpenAlex ID: I4405284683

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

2019 · Hiroyuki Ishiura, Shota Shibata, et al. · Nature Genetics · 442

Effect of Core Stability Training on Trunk Function, Standing Balance, and Mobility in Stroke Patients: A Randomized Controlled Trial

2016 · Koshiro Haruyama, Michiyuki Kawakami, et al. · Neurorehabilitation and neural repair · 258

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33

1993 · T. Toda, M. Segawa, et al. · Nature Genetics · 244

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

2005 · M E Baser, L Kuramoto, et al. · Journal of Medical Genetics · 123

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Circadian rhythm and variability of heart rate in Duchenne-type progressive muscular dystrophy

1995 · Masayuki Yotsukura, Kazuya Sasaki, et al. · The American Journal of Cardiology · 82

Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing

2022 · Satoko Miyatake, Eriko Koshimizu, et al. · npj Genomic Medicine · 81

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Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy

2016 · Satoko Miyatake, Satomi Mitsuhashi, et al. · The American Journal of Human Genetics · 80

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Muscle damage progression in Duchenne muscular dystrophy evaluated by a new quantitative computed tomography method

1993 · Meigen Liu, Naoichi Chino, et al. · Archives of Physical Medicine and Rehabilitation · 74

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses

2014 · Hiroyuki Ishiura, Yuji Takahashi, et al. · Journal of Human Genetics · 71

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Clinical utility of anti-signal recognition particle antibody in the differential diagnosis of myopathies

2008 · S. Suzuki, T. Satoh, et al. · Rheumatology · 69

Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan

2016 · Toshio Saito, Mitsuru Kawai, et al. · Neuromuscular Disorders · 66

Development of a new scale for dysphagia in patients with progressive neuromuscular diseases: the Neuromuscular Disease Swallowing Status Scale (NdSSS)

2015 · Ayako Wada, Michiyuki Kawakami, et al. · Journal of Neurology · 65

Clinical Care Recommendations for Cardiologists Treating Adults With Myotonic Dystrophy

2020 · Elizabeth M. McNally, Douglas L. Mann, et al. · Journal of the American Heart Association · 63

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The Shift of Residents From University to Non-University Hospitals in Japan: A Survey Study

2008 · Kyoko Nomura, Eiji Yano, et al. · Journal of General Internal Medicine · 45

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Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis

2018 · Yuko Shimizu-Motohashi, Terumi Murakami, et al. · Orphanet Journal of Rare Diseases · 43

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Switching Tenofovir/Emtricitabine plus Lopinavir/r to Raltegravir plus Darunavir/r in Patients with Suppressed Viral Load Did Not Result in Improvement of Renal Function but Could Sustain Viral Suppression: A Randomized Multicenter Trial

2013 · Takeshi Nishijima, Hiroyuki Gatanaga, et al. · PLoS ONE · 41

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Decreased resting energy expenditure in patients with Duchenne muscular dystrophy

2011 · Mami Shimizu-Fujiwara, Hirofumi Komaki, et al. · Brain and Development · 41

Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome

2021 · Satoko Miyatake, Kunihiro Yoshida, et al. · Brain · 38

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Necklace cytoplasmic bodies in hereditary myopathy with early respiratory failure

2014 · Akinori Uruha, Yukiko K Hayashi, et al. · Journal of Neurology Neurosurgery & Psychiatry · 36

Asymptomatic Sporadic Dysferlinopathy Presenting with Elevation of Serum Creatine Kinase. Typical Distribution of Muscle Involvement Shown by MRI but not by CT

2008 · Satomi Okahashi, Go Ogawa, et al. · Internal Medicine · 36

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Early phase 2 trial of TAS‐205 in patients with Duchenne muscular dystrophy

2020 · Hirofumi Komaki, Yoshihiro Maegaki, et al. · Annals of Clinical and Translational Neurology · 35

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High-Dose Ubiquinol Supplementation in Multiple-System Atrophy: A Multicentre, Randomised, Double-Blinded, Placebo-Controlled Phase 2 Trial

2022 · Jun Mitsui, Takashi Matsukawa, et al. · EClinicalMedicine · 34

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Three-dimensional structure of the human cerebellar dentate nucleus: a computerized reconstruction study

1997 · K. Yamaguchi, Noboru Goto · Anatomy and Embryology · 34

Natural history of Becker muscular dystrophy: a multicenter study of 225 patients

2023 · Akinori Nakamura, Tsuyoshi Matsumura, et al. · Annals of Clinical and Translational Neurology · 33

RNA-seq analysis, targeted long-read sequencing and in silico prediction to unravel pathogenic intronic events and complicated splicing abnormalities in dystrophinopathy

2022 · Mariko Okubo, Satoru Noguchi, et al. · Human Genetics · 33

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Works count: 288

Citation count: 5,987