Mikiya Suzuki

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

Satoko Miyatake, Satomi Mitsuhashi, Yukiko Hayashi et al. · The American Journal of Human Genetics · 2016 · 81 citations · Full text

Medicine, Genetics, Molecular Genetics +9

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

Hiroyuki Ishiura, Yuji Takahashi, Toshihiro Hayashi et al. · Journal of Human Genetics · 2014 · 68 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

Satomi Okahashi, Go Ogawa, Mikiya Suzuki et al. · Internal Medicine · 2008 · 33 citations · Full text

Medicine, Neurology, Pathology +13

Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1

Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura et al. · Journal of the American Heart Association · 2020 · 21 citations · Full text

Medicine, Cardiology, Internal Medicine +11

Mental Retardation and Lifetime Events of Duchenne Muscular Dystrophy in Japan

Hitoshi Mochizuki, Satoko Miyatake, Mikiya Suzuki et al. · Internal Medicine · 2008 · 19 citations · Full text

Medicine, Internal Medicine, Movement Disorders +9