Mitsunori Watanabe

E. Matsubara, M. Shoji, Mitsunori Watanabe, 2012, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, γ‐globulin, and α‐fetoprotein

M. Koenig, M. Shoji, K. Okamoto, 1998 .

Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan

K. Okamoto, Mitsunori Watanabe, Y. Ikeda, 2000, Neurology.

Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis

Y. Itoyama, M. Shoji, K. Okamoto, 1997, Journal of the Neurological Sciences.

Interaction of PDZRhoGEF with Microtubule-associated Protein 1 Light Chains

J. Rothstein, Mitsunori Watanabe, M. Jackson, 2006, Journal of Biological Chemistry.

Familial amyloid polyneuropathy (Finnish type) in a Japanese family: Clinical features and immunocytochemical studies

K. Okamoto, Mitsunori Watanabe, M. Takatama, 2007, Journal of the Neurological Sciences.

Loss of β-III Spectrin Leads to Purkinje Cell Dysfunction Recapitulating the Behavior and Neuropathology of Spinocerebellar Ataxia Type 5 in Humans

M. Dutia, J. Rothstein, A. Lyndon, 2010, The Journal of Neuroscience.

Histological Evidence of Protein Aggregation in Mutant SOD1 Transgenic Mice and in Amyotrophic Lateral Sclerosis Neural Tissues

D. Price, P. Wong, J. Rothstein, 2001, Neurobiology of Disease.

Amyloid β-protein ending at Thr43 is a minor component of some diffuse plaques in the Alzheimer's disease brain, but is not found in cerebrovascular amyloid

S. Hirai, M. Shoji, T. Iizuka, 1995, Brain Research.

Membranous cytoplasmic bodies in the anterior horn neurons in two patients with amyotrophic lateral sclerosis

S. Hirai, K. Okamoto, M. Amari, 1996 .

Combination assay of CSF Tau, Aβ1-40 and Aβ1-42(43) as a biochemical marker of Alzheimer's disease

S. Hirai, E. Matsubara, M. Shoji, 1998, Journal of the Neurological Sciences.

Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double‐transgenic mouse model

D. Westaway, E. Matsubara, M. Shoji, 2010, Journal of neuroscience research.

Fundamental Morphological Changes in Human Olivary Hypertrophy

S. Hirai, Koichi E. Okamoto, Mitsunori Watanabe, 1992, Acta pathologica japonica.

A Japanese family with adrenoleukodystrophy with a codon 291 deletion: a clinical, biochemical, pathological, and genetic report

S. Tsuji, M. Shoji, K. Okamoto, 1998, Journal of Neurological Sciences.

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.

Cerebrospinal fluid tau in dementia disorders: a large scale multicenter study by a Japanese study group

S. Hirai, K. Nakashima, H. Arai, 2002, Neurobiology of Aging.

Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease

Y. Itoyama, S. Hirai, M. Shoji, 1996, Journal of the Neurological Sciences.

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world

P. Andersen, C. Gellera, M. Savontaus, 2001, European Journal of Human Genetics.

Reuptake of L‐DOPA‐derived extracellular DA in the striatum of a rodent model of Parkinson's disease via norepinephrine transporter

M. Shoji, Mitsunori Watanabe, T. Kawarabayashi, 2008, Synapse.

Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1- 2 polymorphism and contribution to founder effect

M. Shoji, K. Okamoto, Mitsunori Watanabe, 1999, Journal of medical genetics.

Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3

A. Lyndon, E. Matsubara, M. Shoji, 2010, Brain Research.

Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI

Mikio Shoji, Mitsunori Watanabe, Koichi Okamoto, 2000, Journal of the Neurological Sciences.

Intracellular generation of amyloid β protein from amyloid β protein precursor fragment by direct cleavage with β- and γ-secretase

S. Hirai, E. Matsubara, M. Shoji, 1996 .