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Glycaemic control boosts glucosylated nanocarrier crossing the BBB into the brain

Nature communications, 2017-10, Vol.8 (1), p.1001-9, Article 1001

2017

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Prion encephalopathies

Journal of the neurological sciences, 2015-10, Vol.357, p.e467-e467

Mizusawa, H

2015

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Burden and genetics of Parkinson’s disease in Asian Oceanian Region

Journal of the neurological sciences, 2015-10, Vol.357, p.e490-e490

Mizusawa, H

2015

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Environmental challenges for the nervous system and the brain in Japan

Revue neurologique, 2019-12, Vol.175 (10), p.693-697

2019

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White Matter Alteration in Idiopathic Normal Pressure Hydrocephalus: Tract-Based Spatial Statistics Study

American journal of neuroradiology : AJNR, 2012-01, Vol.33 (1), p.97-103

2012

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Significance of Development and Reversion of Collaterals on MRI in Early Neurologic Improvement and Long-Term Functional Outcome after Intravenous Thrombolysis for Ischemic Stroke

American journal of neuroradiology : AJNR, 2015-10, Vol.36 (10), p.1839-1845

2015

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Altered Microstructure in Corticospinal Tract in Idiopathic Normal Pressure Hydrocephalus: Comparison with Alzheimer Disease and Parkinson Disease with Dementia

American journal of neuroradiology : AJNR, 2011-10, Vol.32 (9), p.1681-1687

2011

Volltextzugriff (PDF)

COVID-19 international neurological registries

Lancet neurology, 2020-06, Vol.19 (6), p.484-485

2020

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Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation?

Journal of neurology, neurosurgery and psychiatry, 2014-01, Vol.85 (1), p.85-91

2014

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Iatrogenic abeta transmission

Journal of the neurological sciences, 2019-10, Vol.405, p.65-65

Mizusawa, H.

2019

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Specific clinical signs and symptoms are predictive of clinical course in sporadic Creutzfeldt−Jakob disease

European journal of neurology, 2016-09, Vol.23 (9), p.1455-1462

2016

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Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

Neurology, 2011-11, Vol.77 (20), p.1853

2011

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Efficacy and safety of leuprorelin acetate for subjects with spinal and bulbar muscular atrophy: pooled analyses of two randomized-controlled trials

Journal of neurology, 2019-05, Vol.266 (5), p.1211-1221

2019

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Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation

Cell death and differentiation, 2007-12, Vol.14 (12), p.2058-2067

2007

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Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease

American journal of neuroradiology : AJNR, 2012-02, Vol.33 (2), p.274-279

2012

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Defining the future of neurology - Japan, Asia and Oceania

Journal of the neurological sciences, 2017-10, Vol.381, p.13-13

Mizusawa, H.

2017

Volltextzugriff (PDF)

Prion disease: An overview

Journal of the neurological sciences, 2017-10, Vol.381, p.25-25

Mizusawa, H.

2017

Volltextzugriff (PDF)

(123)I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson's disease

Journal of neurology, neurosurgery and psychiatry, 1999-08, Vol.67 (2), p.189-194

1999

Volltextzugriff (PDF)

Relationship and factor structure in multisystem neurodegeneration in Parkinson's disease

Acta neurologica Scandinavica, 2014-12, Vol.130 (6), p.347-353

2014

Volltextzugriff (PDF)

Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease

Neurology, 2007-07, Vol.69 (4), p.360

2007

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Spinal cord ring enhancement in patients with neuromyelitis optica

Acta neurologica Scandinavica, 2015-07, Vol.132 (1), p.37-41

2015

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Chronic inflammatory demyelinating polyneuropathy: decreased claudin-5 and relocated ZO-1

Journal of neurology, neurosurgery and psychiatry, 2004-05, Vol.75 (5), p.765-769

2004

Volltextzugriff (PDF)

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease

Neurology, 2005-02, Vol.64 (4), p.643

2005

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Clinical and epidemiological survey of gerstmann-sträussler-scheinker disease with codon 102 mutation in Japan

Journal of the neurological sciences, 2015-10, Vol.357, p.e114-e114

2015

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Human prion diseases in Japan: a prospective surveillance from 1999

Journal of the neurological sciences, 2015-10, Vol.357, p.e137-e137

2015

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Glycaemic control boosts glucosylated nanocarrier crossing the BBB into the brain

Prion encephalopathies

Burden and genetics of Parkinson’s disease in Asian Oceanian Region

Environmental challenges for the nervous system and the brain in Japan

White Matter Alteration in Idiopathic Normal Pressure Hydrocephalus: Tract-Based Spatial Statistics Study

Significance of Development and Reversion of Collaterals on MRI in Early Neurologic Improvement and Long-Term Functional Outcome after Intravenous Thrombolysis for Ischemic Stroke

Altered Microstructure in Corticospinal Tract in Idiopathic Normal Pressure Hydrocephalus: Comparison with Alzheimer Disease and Parkinson Disease with Dementia

COVID-19 international neurological registries

Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation?

Iatrogenic abeta transmission

Specific clinical signs and symptoms are predictive of clinical course in sporadic Creutzfeldt−Jakob disease

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

Efficacy and safety of leuprorelin acetate for subjects with spinal and bulbar muscular atrophy: pooled analyses of two randomized-controlled trials

Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation

Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease

Defining the future of neurology - Japan, Asia and Oceania

Prion disease: An overview

(123)I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson's disease

Relationship and factor structure in multisystem neurodegeneration in Parkinson's disease

Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease

Spinal cord ring enhancement in patients with neuromyelitis optica

Chronic inflammatory demyelinating polyneuropathy: decreased claudin-5 and relocated ZO-1

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease

Clinical and epidemiological survey of gerstmann-sträussler-scheinker disease with codon 102 mutation in Japan

Human prion diseases in Japan: a prospective surveillance from 1999

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