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Lower Cranial Dystonia with Inflated Cheeks: A Case of Dystonic Respiratory Failure

Internal Medicine, 2023/06/01, Vol.62(11), pp.1671-1674

2023

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Intracellular Aβ42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

The FASEB journal, 2005-02, Vol.19 (2), p.1-29

2005

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Coexistence of Huntington’s disease and amyotrophic lateral sclerosis: a clinicopathologic study

Acta neuropathologica, 2012-11, Vol.124 (5), p.749-760

2012

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Reader response: Lymphoplasmacyte-rich meningioma involving the whole intracranial dura mater

Neurology, 2019-03, Vol.92 (10), p.494-494

2019

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Prefrontal Abnormality of Schizophrenia Revealed by DNA Microarray: Impact on Glial and Neurotrophic Gene Expression

Annals of the New York Academy of Sciences, 2004-10, Vol.1025 (1), p.84-91

2004

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Lower Cranial Dystonia with Inflated Cheeks: A Case of Dystonic Respiratory Failure

Internal Medicine, 2023, pp.9554-22

2023

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Autotaxin expression is enhanced in frontal cortex of Alzheimer-type dementia patients

Neuroscience letters, 2006-05, Vol.400 (1), p.97-100

2006

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p.Asn77Lys homozygous CLN6 mutation in two unrelated Japanese patients with Kufs disease, an adult onset neuronal ceroid lipofuscinosis

Clinica chimica acta, 2021-12, Vol.523, p.191-195

2021

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Brain hydrogen sulfide is severely decreased in Alzheimer's disease

Biochemical and biophysical research communications, 2002-05, Vol.293 (5), p.1485-1488

2002

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A decrease in interleukin-1 receptor antagonist expression in the prefrontal cortex of schizophrenic patients

Neuroscience research, 2003-07, Vol.46 (3), p.299-307

2003

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Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses

Neuropathology, 2016-08, Vol.36 (4), p.405-410

2016

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A neuropathological study of autosomal-dominant chorea-acanthocytosis with a mutation of VPS13A

Acta neuropathologica, 2009, Vol.117 (1), p.85-94

2009

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Distinct Pathological Features of the Gallyas- and Tau-positive Glia in the Parkinsonism-Dementia Complex and Amyotrophic Lateral Sclerosis of Guam

Journal of neuropathology and experimental neurology, 1997-03, Vol.56 (3), p.308-316

1997

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Progressive supranuclear palsy on Guam

Acta neuropathologica, 2001-11, Vol.102 (5), p.510-514

2001

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Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases

FEBS letters, 2005-05, Vol.579 (13), p.2948-2952

2005

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Amyotrophic lateral sclerosis of Guam: the nature of the neuropathological findings

Acta neuropathologica, 1994-11, Vol.88 (5), p.405-412

1994

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Selective reduction of a PDZ protein, SAP‐97, in the prefrontal cortex of patients with chronic schizophrenia

Journal of neurochemistry, 2002-11, Vol.83 (4), p.797-806

2002

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Development and characterization of a TAPIR-like mouse monoclonal antibody to amyloid-beta

Journal of Alzheimer's disease, 2008-06, Vol.14 (2), p.161-173

2008

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Glypican‐1 as an Aβ binding HSPG in the human brain: Its localization in DIG domains and possible roles in the pathogenesis of Alzheimer's disease

The FASEB journal, 2004-06, Vol.18 (9), p.1013-1015

2004

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Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

Annals of neurology, 2004-02, Vol.55 (2), p.241-249

2004

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The anterolateral funiculus in the spinal cord in amyotrophic lateral sclerosis

Acta neuropathologica, 1995-09, Vol.90 (3), p.221-227

1995

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Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2

The Journal of biological chemistry, 2001-01, Vol.276 (3), p.2108-2114

2001

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Pure akinesia manifested neuroleptic malignant syndrome : a clinical variant of progressive supranuclear palsy

Acta neuropathologica, 1997-03, Vol.93 (3), p.306-309

1997

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Systemic mastocytosis and recurrent anaphylactic shock

The Lancet (British edition), 2002-06, Vol.359 (9323), p.2084-2084

2002

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Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1

Advances in experimental medicine and biology, 2010, Vol.685, p.21

2010

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Lower Cranial Dystonia with Inflated Cheeks: A Case of Dystonic Respiratory Failure

Intracellular Aβ42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

Coexistence of Huntington’s disease and amyotrophic lateral sclerosis: a clinicopathologic study

Reader response: Lymphoplasmacyte-rich meningioma involving the whole intracranial dura mater

Prefrontal Abnormality of Schizophrenia Revealed by DNA Microarray: Impact on Glial and Neurotrophic Gene Expression

Lower Cranial Dystonia with Inflated Cheeks: A Case of Dystonic Respiratory Failure

Autotaxin expression is enhanced in frontal cortex of Alzheimer-type dementia patients

p.Asn77Lys homozygous CLN6 mutation in two unrelated Japanese patients with Kufs disease, an adult onset neuronal ceroid lipofuscinosis

Brain hydrogen sulfide is severely decreased in Alzheimer's disease

A decrease in interleukin-1 receptor antagonist expression in the prefrontal cortex of schizophrenic patients

Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses

A neuropathological study of autosomal-dominant chorea-acanthocytosis with a mutation of VPS13A

Distinct Pathological Features of the Gallyas- and Tau-positive Glia in the Parkinsonism-Dementia Complex and Amyotrophic Lateral Sclerosis of Guam

Progressive supranuclear palsy on Guam

Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases

Amyotrophic lateral sclerosis of Guam: the nature of the neuropathological findings

Selective reduction of a PDZ protein, SAP‐97, in the prefrontal cortex of patients with chronic schizophrenia

Development and characterization of a TAPIR-like mouse monoclonal antibody to amyloid-beta

Glypican‐1 as an Aβ binding HSPG in the human brain: Its localization in DIG domains and possible roles in the pathogenesis of Alzheimer's disease

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

The anterolateral funiculus in the spinal cord in amyotrophic lateral sclerosis

Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2

Pure akinesia manifested neuroleptic malignant syndrome : a clinical variant of progressive supranuclear palsy

Systemic mastocytosis and recurrent anaphylactic shock

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1

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