Get started
Author

Satoshi Kuru

Expression of tumor necrosis factor-α in regenerating muscle fibers in inflammatory and non-inflammatory myopathies
2003 · Satoshi Kuru, Akira Inukai, et al. · Acta Neuropathologica · 114
Carvedilol can Prevent Cardiac Events in Duchenne Muscular Dystrophy
2010 · Tsuyoshi Matsumura, Takuhisa Tamura, et al. · Internal Medicine · 81
PDF
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
PDF
An autopsy case of spinal muscular atrophy type III (Kugelberg‐Welander disease)
2008 · Satoshi Kuru, Motoko Sakai, et al. · Neuropathology · 79
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
[A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy].
2004 · Satoshi Kuru, Fumihiko Yasuma, et al. · PubMed · 40
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
PDF
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
Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology
2022 · Koyo Tsujikawa, Kohei Hamanaka, et al. · Science Advances · 33
Milder forms of muscular dystrophy associated with POMGNT2 mutations
2015 · Yukari Endo, Mingrui Dong, et al. · Neurology Genetics · 30
PDF
XPA Gene Mutations Resulting in Subtle Truncation of Protein in Xeroderma Pigmentosum Group A Patients with Mild Skin Symptoms
2010 · Yoshito Takahashi, Yoko Endo, et al. · Journal of Investigative Dermatology · 30
A new lease on life for patients with Duchenne muscular dystrophy in Japan
2004 · Fumihiko Yasuma, Masaaki Konagaya, et al. · The American Journal of Medicine · 29
Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter
2005 · Satoshi Kuru, Motoko Sakai, et al. · Neuropathology · 28
Independent distribution between tauopathy secondary to subacute sclerotic panencephalitis and measles virus: An immunohistochemical analysis in autopsy cases including cases treated with aggressive antiviral therapies
2022 · Hiroaki Miyahara, Akio Akagi, et al. · Brain Pathology · 22
PDF
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1
2020 · Hideki Itoh, Takashi Hisamatsu, et al. · Journal of the American Heart Association · 22
Muscle development in healthy children evaluated by bioelectrical impedance analysis
2016 · Tomoka Uchiyama, Takahiro Nakayama, et al. · Brain and Development · 17
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosis
2021 · Genki Tohnai, Ryoichi Nakamura, et al. · Neurobiology of Aging · 15
PDF
A recurrent homozygous ACTN2 variant associated with core myopathy
2021 · Michio Inoue, Satoru Noguchi, et al. · Acta Neuropathologica · 15
PDF
Dilated Cardiomyopathy in Kugelberg-Welander Disease: Coexisting Sleep Disordered Breathing and Its Treatment with Continuous Positive Airway Pressure
2004 · Fumihiko YASUMA, Satoshi KURU, et al. · Internal Medicine · 15
PDF
[Two cases of Duchenne muscular dystrophy complicated with dilated cardiomyopathy and cerebral infarction].
2006 · Chizuru Ikeniwa, Motoko Sakai, et al. · PubMed · 14
Tranilast for advanced heart failure in patients with muscular dystrophy: a single-arm, open-label, multicenter study
2022 · Tsuyoshi Matsumura, Hiroya Hashimoto, et al. · Orphanet Journal of Rare Diseases · 12
PDF
0251 Effect of intermittent positive pressure ventilation on life-span and causes of death in Duchenne muscular dystrophy
2005 · Masaaki Konagaya, Motoko Sakai, et al. · Journal of the Neurological Sciences · 12
The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathy
2020 · Takashi Ando, Ryoichi Nakamura, et al. · Neurobiology of Aging · 11
PDF
Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene
2014 · Akinori Nakamura, Satoshi Kuru, et al. · Neurobiology of Aging · 11
A clinical and pathological study of a Japanese case of Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex with family history
2003 · Masaaki Konagaya, Takashi Kato, et al. · Journal of Neurology · 11
Works count: 83
Citation count: 1,031
H-index: 16
I10-index: 28
Year
Topic
Type