Y. Momose

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.

Toward identification of susceptibility genes for sporadic Parkinson’s disease

H. Inoko, N. Hattori, G. Tamiya, 2003, Journal of Neurology.

Variants associated with Gaucher disease in multiple system atrophy

J. Trojanowski, S. Gilman, Y. Kuroiwa, 2015, Annals of clinical and translational neurology.

Multiplex families with multiple system atrophy.

I. Kanazawa, S. Tsuji, A. Kakita, 2007, Archives of neurology.

Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation

S. Tsuji, J. Hamada, Yuji Takahashi, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Effects of dietary protein levels on performance of Japanese quail

Y. Momose, K. Tomizawa, Emiko Watanabe, 1993 .

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.

H. Inoko, N. Hattori, S. Murayama, 2006, Human molecular genetics.

Appropriate data cleaning methods for genome-wide association study

S. Tsuji, A. Koike, A. Fujimoto, 2008, Journal of Human Genetics.

[Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease].

S. Tsuji, J. Goto, Y. Shirota, 2009, Rinsho shinkeigaku = Clinical neurology.

Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms

Ichiro Kanazawa, Tatsushi Toda, Miho Murata, 2002, Annals of neurology.

Attitude of outpatients with neuromuscular diseases in Japan to pain and use of analgesics

M. Miyashita, Y. Ichikawa, K. Kazuma, 2008, Journal of the Neurological Sciences.

A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations

A. Hida, I. Kanazawa, S. Tsuji, 2009, Movement disorders : official journal of the Movement Disorder Society.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

Sliding balloon technique to treat acute severe sinus thrombosis: a technical case report

Y. Momose, Akihiro Nemoto, M. Morimoto, 2011 .

Congenital long QT syndrome presenting with a history of epilepsy: Misdiagnosis or relationship between channelopathies of the heart and brain?

Y. Momose, C. Omichi, S. Kitahara, 2010, Epilepsia.