Mikiya Suzuki

发表

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

J. Towbin, I. Nonaka, Y. Hayashi, 2017, American journal of human genetics.

The characteristics of camptocormia in patients with Parkinson's disease: A large cross-sectional multicenter study in Japan

K. Kuroda, K. Mizoguchi, K. Hasegawa, 2015, Journal of the Neurological Sciences.

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

M. Horie, S. Suwazono, S. Sasaki, 2020, Journal of the American Heart Association.

Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions

I. Nishino, M. Sasaki, N. Minami, 2017, Neuromuscular Disorders.

Asymptomatic sporadic dysferlinopathy presenting with elevation of serum creatine kinase. Typical distribution of muscle involvement shown by MRI but not by CT.

I. Nishino, S. Okahashi, G. Ogawa, 2008, Internal medicine.

Mental retardation and lifetime events of Duchenne muscular dystrophy in Japan.

H. Mochizuki, S. Miyatake, T. Tamura, 2008, Internal medicine.

[Inpatients with facioscapulohumeral muscular dystrophy in specialized institutions in Japan from 1999 to 2013-Clinical condition changes and causes of death].

Toshio Saito, Toshiaki Takahashi, S. Kuru, 2019, Rinsho shinkeigaku = Clinical neurology.

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

I. Kanazawa, S. Tsuji, Toshihiro Hayashi, 2014, Journal of Human Genetics.

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

I. Kanazawa, S. Tsuji, Toshihiro Hayashi, 2014, Journal of Human Genetics.

Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes

I. Nishino, S. Morishita, M. Yamaguchi, 2022, Journal of Neurology.

A Japanese male with a novel ANO5 mutation with minimal muscle weakness and muscle pain till his late fifties

I. Nonaka, I. Nishino, K. Kaida, 2017, Neuromuscular Disorders.

Brain volume analyses and somatosensory evoked potentials in multiple system atrophy

Yoshikazu Ugawa, Hitoshi Mochizuki, Hajime Tanabe, 2010, Journal of Neurology.

[An experience of administration of modafinil for excessive daytime sleepiness in a patient with myotonic dystorophy].

Y. Oya, M. Kawai, Mikiya Suzuki, 2010, Rinsho shinkeigaku = Clinical neurology.

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

J. Towbin, I. Nonaka, Y. Hayashi, 2017, American journal of human genetics.