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Elevated serum pentraxin 3 levels might predict the diagnosis of branch atheromatous disease at a very early stage

European journal of neurology, 2020-07, Vol.27 (7), p.1279-1284

2020

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Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation

European journal of neurology, 2017-01, Vol.24 (1), p.37-45

2017

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Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation

European journal of neurology, 2018-01, Vol.25 (1), p.142-147

2018

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iPatax: iPad® application software for evaluating ataxia

Journal of the neurological sciences, 2017-10, Vol.381, p.889-889

2017

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Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia

American journal of neuroradiology : AJNR, 2017-01, Vol.38 (1), p.77-83

2017

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The phenotype spectrum of Japanese multiple system atrophy

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.1253-1255

2010

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Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families

Neurology, 2008-08, Vol.71 (8), p.547-551

2008

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A novel mutation in the HTRA1 gene causes CARASIL without alopecia

Neurology, 2011-04, Vol.76 (15), p.1353-1355

2011

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Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease

Journal of neurology, neurosurgery and psychiatry, 2009-09, Vol.80 (9), p.1050-1052

2009

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Generation of intracellular domain of insulin receptor tyrosine kinase by γ-secretase

Biochemical and biophysical research communications, 2007-08, Vol.360 (1), p.90-96

2007

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Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Brain (London, England : 1878), 2003-01, Vol.126 (1), p.134-151

2003

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Co-occurrence of argyrophilic grain disease in sporadic amyotrophic lateral sclerosis

Neuropathology and applied neurobiology, 2012-02, Vol.38 (1), p.54-60

2012

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Neuroaxonal integrity evaluated by MR spectroscopy in a case of CARASIL

Journal of neurology, neurosurgery and psychiatry, 2011-08, Vol.82 (8), p.860-861

2011

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Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia

Journal of medical genetics, 2007-12, Vol.44 (12), p.772-778

2007

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Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP

Neurology, 2005-04, Vol.64 (8), p.1471-1475

2005

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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

Nature genetics, 1994-01, Vol.6 (1), p.9-13

1994

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Beta-synuclein gene alterations in dementia with Lewy bodies

Neurology, 2004-09, Vol.63 (5), p.805-811

2004

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Amino acid sequences flanking polyglutamine stretches influence their potential for aggregate formation

Neuroreport, 2001-10, Vol.12 (15), p.3357-3364

2001

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Age associated axonal features in HNPP with 17p11.2 deletion in Japan

Journal of neurology, neurosurgery and psychiatry, 2005-08, Vol.76 (8), p.1109-1114

2005

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Interplay of (inter)subjectivity and social norm

Journal of historical pragmatics, 2007-01, Vol.8 (2), p.239-267

Onodera, Noriko O.

2007

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Polyglutamine Diseases: Where does Toxicity Come from? What is Toxicity? Where are We Going?

Journal of molecular cell biology, 2010-08, Vol.2 (4), p.180-191

2010

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Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5

Neurology, 2004-05, Vol.62 (9), p.1601-1603

2004

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The gene for Machado-Joseph disease maps to human chromosome 14q

Nature genetics, 1993-07, Vol.4 (3), p.300-304

1993

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Experimental investigation on tunnel sonic boom

Shock waves, 1995-10, Vol.5 (3), p.127-138

1995

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New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2

Neurology, 2006-04, Vol.66 (8), p.1251-1252

2006

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Elevated serum pentraxin 3 levels might predict the diagnosis of branch atheromatous disease at a very early stage

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation

Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation

iPatax: iPad® application software for evaluating ataxia

Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia

The phenotype spectrum of Japanese multiple system atrophy

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families

A novel mutation in the HTRA1 gene causes CARASIL without alopecia

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease

Generation of intracellular domain of insulin receptor tyrosine kinase by γ-secretase

Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Co-occurrence of argyrophilic grain disease in sporadic amyotrophic lateral sclerosis

Neuroaxonal integrity evaluated by MR spectroscopy in a case of CARASIL

Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia

Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

Beta-synuclein gene alterations in dementia with Lewy bodies

Amino acid sequences flanking polyglutamine stretches influence their potential for aggregate formation

Age associated axonal features in HNPP with 17p11.2 deletion in Japan

Interplay of (inter)subjectivity and social norm

Polyglutamine Diseases: Where does Toxicity Come from? What is Toxicity? Where are We Going?

Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5

The gene for Machado-Joseph disease maps to human chromosome 14q

Experimental investigation on tunnel sonic boom

New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2

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