H. Soma

发表

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

J. Trojanowski, S. Gilman, K. Shirahige, 2013, The New England journal of medicine.

Investigating a novel hepatoprotective substance from ume extract (heated Japanese apricot juice concentrate). Part 1: Finding an active substance using a liver injury rat model

T. Kagawa, H. Soma, K. Hiraishi, 2021, NFS Journal.

Executive dysfunction in patients with spinocerebellar ataxia type 3

Itaru Tamura, F. Moriwaka, H. Soma, 2018, Journal of Neurology.

Estimation of skeletal muscle energy metabolism in Machado‐Joseph disease using 31P‐MR spectroscopy

S. Terae, H. Sasaki, K. Tha, 2011, Movement disorders : official journal of the Movement Disorder Society.

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.

Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 Genes

H. Sasaki, H. Soma, I. Yabe, 2008, Movement disorders : official journal of the Movement Disorder Society.

Microstructural white matter abnormalities of multiple system atrophy: in vivo topographic illustration by using diffusion-tensor MR imaging.

H. Shirato, S. Terae, K. Kudo, 2010, Radiology.

No association between FMR1 premutations and multiple system atrophy

H. Sasaki, H. Soma, I. Yabe, 2004, Journal of Neurology.

[Reliability of the Japanese version of the Scale for the Assessment and Rating of Ataxia (SARA)].

G. Sobue, K. Nakashima, T. Shimohata, 2009, Brain and nerve = Shinkei kenkyu no shinpo.

MSA-C is the predominant clinical phenotype of MSA in Japan: Analysis of 142 patients with probable MSA

H. Sasaki, H. Soma, I. Yabe, 2006, Journal of the Neurological Sciences.

Instructions for use Title Heredity in Multiple System Atrophy

H. Sasaki, H. Soma, I. Yabe, 2016 .

Short communication Heredity in multiple system atrophy

H. Sasaki, H. Soma, I. Yabe, 2006 .

X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter.

H. Sasaki, H. Soma, I. Yabe, 2007, Internal medicine.

Cat Scratch Disease-associated Encephalitis Followed by Parkinsonism

H. Soma, I. Yabe, S. Ura, 2022, Internal medicine.

Investigating a novel hepatoprotective substance from ume extract (heated Japanese apricot juice concentrate). Part 2: Elucidation of chemical structure

T. Kagawa, H. Soma, K. Hiraishi, 2021, NFS Journal.

Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families

H. Sasaki, H. Soma, I. Yabe, 2007, Journal of Human Genetics.

Four mutations of the spastin gene in Japanese families with spastic paraplegia

H. Tachibana, H. Sasaki, S. Kuzuhara, 2006, Journal of Human Genetics.

Usefulness of the Scale for Assessment and Rating of Ataxia (SARA)

H. Sasaki, H. Soma, I. Yabe, 2008, Journal of the Neurological Sciences.

Unusual retinal phenotypes in an SCA7 family.

H. Sasaki, H. Soma, I. Yabe, 2009, Internal medicine.

Hyperintense putaminal rim at 1.5 T: prevalence in normal subjects and distinguishing features from multiple system atrophy

H. Shirato, S. Terae, H. Sasaki, 2012, BMC Neurology.

Heredity in multiple system atrophy

Naoto Fujiki, H. Sasaki, H. Soma, 2006, Journal of the Neurological Sciences.

Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family

S. Saitoh, M. Kitagawa, H. Sasaki, 2008, Journal of Neurology.

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.

A case of pure autotopagnosia following Creutzfeldt–Jakob disease

Itaru Tamura, K. Tashiro, F. Moriwaka, 2016, Cognitive neuropsychology.