PubRank

Mari Yoshida

Author PubWeight™ 104.35‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 2006 10.69
2 The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy. Brain 2005 3.65
3 Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann Neurol 2008 3.13
4 Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n. Am J Hum Genet 2009 1.96
5 Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS. FEBS Lett 2008 1.76
6 RGMa modulates T cell responses and is involved in autoimmune encephalomyelitis. Nat Med 2011 1.71
7 An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains. Am J Hum Genet 2005 1.59
8 Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis. Ann Neurol 2005 1.59
9 Clinical and neuropathological correlates of Lewy body disease. Acta Neuropathol 2003 1.58
10 Distribution of major histocompatibility complex class II-positive microglia and cytokine profile of Parkinson's disease brains. Acta Neuropathol 2003 1.57
11 Transition metal abnormalities in progressive dementias. Biometals 2011 1.51
12 Prion-like properties of pathological TDP-43 aggregates from diseased brains. Cell Rep 2013 1.49
13 Efficacy of mefloquine to progressive multifocal leukoencephalopathy initially presented with parkinsonism. Clin Neurol Neurosurg 2011 1.45
14 Early pathologic changes in hereditary diffuse leukoencephalopathy with spheroids. J Neuropathol Exp Neurol 2014 1.38
15 Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients. Brain 2005 1.33
16 Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay. PLoS One 2013 1.30
17 Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis. J Neurol 2011 1.29
18 Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease. Acta Neuropathol 2005 1.14
19 Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy. Neuropathology 2010 1.04
20 Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt-Jakob disease patients. J Neuroimmunol 2012 1.03
21 The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement. Am J Hum Genet 2012 1.02
22 VZV vasculopathy associated with myelo-radiculoganglio-meningo-encephalitis: an autopsy case of an immunocompetent 66-year-old male. J Neurol Sci 2008 1.01
23 Cytokine production of activated microglia and decrease in neurotrophic factors of neurons in the hippocampus of Lewy body disease brains. Acta Neuropathol 2004 0.96
24 CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy. Am J Med Genet B Neuropsychiatr Genet 2012 0.96
25 HTLV-1 induces a Th1-like state in CD4+CCR4+ T cells. J Clin Invest 2014 0.94
26 [Is hypertrophic pachymeningitis a dural lesion of IgG4-related systemic disease?]. Rinsho Shinkeigaku 2009 0.92
27 Acute motor and sensory neuronopathy associated with small-cell lung cancer: a clinicopathological study. Neuropathology 2006 0.92
28 Ubiquilin immunoreactivity in cytoplasmic and nuclear inclusions in synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease. Acta Neuropathol 2012 0.92
29 Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy. J Neurol Neurosurg Psychiatry 2013 0.92
30 Positive feedback loop via astrocytes causes chronic inflammation in virus-associated myelopathy. Brain 2013 0.91
31 An autopsied case of progressive supranuclear palsy presenting with cerebellar ataxia and severe cerebellar involvement. Neuropathology 2013 0.90
32 ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19. Am J Hum Genet 2013 0.90
33 An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease). Neuropathology 2008 0.90
34 Characteristics of alpha-synucleinopathy in centenarians. Acta Neuropathol 2006 0.90
35 Molecular dissection of TDP-43 proteinopathies. J Mol Neurosci 2011 0.89
36 Molecular analysis and biochemical classification of TDP-43 proteinopathy. Brain 2012 0.89
37 An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type. Neuropathology 2011 0.88
38 Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62. Neurosci Lett 2003 0.88
39 Extensive aggregation of α-synuclein and tau in juvenile-onset neuroaxonal dystrophy: an autopsied individual with a novel mutation in the PLA2G6 gene-splicing site. Acta Neuropathol Commun 2013 0.87
40 MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology. Neuropathology 2008 0.87
41 Argyrophilic grain disease: frequency and neuropathology in centenarians. Acta Neuropathol 2006 0.87
42 Degeneration of the inferior olive in spinocerebellar ataxia 6 may depend on disease duration: report of two autopsy cases and statistical analysis of autopsy cases reported to date. Neuropathology 2005 0.86
43 Quality control of photosystem II: FtsH hexamers are localized near photosystem II at grana for the swift repair of damage. J Biol Chem 2010 0.86
44 Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein. Acta Neuropathol Commun 2013 0.85
45 Quality control of Photosystem II: cleavage and aggregation of heat-damaged D1 protein in spinach thylakoids. Biochim Biophys Acta 2007 0.85
46 Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease. Neuropathology 2008 0.85
47 alpha-Synuclein-immunoreactive structure formation is enhanced in sympathetic ganglia of patients with multiple system atrophy. Acta Neuropathol 2005 0.84
48 Gene expressions specifically detected in motor neurons (dynactin 1, early growth response 3, acetyl-CoA transporter, death receptor 5, and cyclin C) differentially correlate to pathologic markers in sporadic amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 2007 0.84
49 Neuropathologic characteristics of spinal cord lesions in sporadic Creutzfeldt-Jakob disease. Acta Neuropathol 2005 0.83
50 An autopsy case of lymphomatosis cerebri showing pathological changes of intravascular large B-cell lymphoma in visceral organs. Neuropathology 2011 0.83
51 Tuft-shaped astrocytes in Lewy body disease. Acta Neuropathol 2005 0.83
52 Optineurin immunoreactivity in neuronal nuclear inclusions of polyglutamine diseases (Huntington's, DRPLA, SCA2, SCA3) and intranuclear inclusion body disease. Acta Neuropathol 2012 0.83
53 Accumulation of the sigma-1 receptor is common to neuronal nuclear inclusions in various neurodegenerative diseases. Neuropathology 2013 0.82
54 Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 2011 0.82
55 Mitochondrial genome structure and evolution in the living fossil vampire squid, Vampyroteuthis infernalis, and extant cephalopods. Mol Phylogenet Evol 2007 0.82
56 Effect of age and sex differences on wild-type transthyretin amyloid formation in familial amyloidotic polyneuropathy: a proteomic approach. Int J Cardiol 2013 0.82
57 [A case of intravascular malignant lymphomatosis presenting as slowly progressive paraplegia]. Brain Nerve 2008 0.81
58 Distribution of astrocytic plaques in the corticobasal degeneration brain and comparison with tuft-shaped astrocytes in the progressive supranuclear palsy brain. Acta Neuropathol 2003 0.81
59 Clinical diagnosis of Creutzfeldt-Jakob disease: accuracy based on analysis of autopsy-confirmed cases. J Neurol Sci 2008 0.81
60 Recurrent limbic and extralimbic encephalitis associated with thymoma. Clin Neurol Neurosurg 2006 0.81
61 Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss. J Neurol Sci 2010 0.81
62 Lewy body-related α-synucleinopathy in the spinal cord of cases with incidental Lewy body disease. Neuropathology 2011 0.81
63 Interleukin-6 enhances manganese accumulation in SH-SY5Y cells: implications of the up-regulation of ZIP14 and the down-regulation of ZnT10. Metallomics 2014 0.80
64 Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter. Neuropathology 2005 0.80
65 Overexpression of hippocampal cholinergic neurostimulating peptide in heterozygous transgenic mice increases the amount of ChAT in the medial septal nucleus. Brain Res 2009 0.80
66 An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein. Neuropathology 2009 0.80
67 Argyrophilic grains are reliable disease-specific features of corticobasal degeneration. J Neuropathol Exp Neurol 2014 0.79
68 Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease. Neuropathology 2007 0.79
69 Widespread spinal cord involvement in progressive supranuclear palsy. Neuropathology 2007 0.79
70 Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations. Clin Neuropathol 2012 0.79
71 Widespread active inflammatory lesions in a case of HTLV-I-associated myelopathy lasting 29 years. Acta Neuropathol 2004 0.79
72 Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type. Acta Neuropathol 2006 0.79
73 Reduction in QSART and vasoactive intestinal polypeptide expression in the skin of Parkinson's disease patients and its relation to dyshidrosis. J Cutan Pathol 2009 0.79
74 Argyrophilic grain disease presenting with frontotemporal dementia: a neuropsychological and pathological study of an autopsied case with presenile onset. Neuropathology 2005 0.78
75 Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease. Neuropathology 2013 0.78
76 Respiratory failure in a patient with antecedent poliomyelitis: amyotrophic lateral sclerosis or post-polio syndrome? Clin Neurol Neurosurg 2005 0.78
77 Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob disease. Neuropathology 2007 0.78
78 Longitudinal study on MRI intensity changes of Machado-Joseph disease: correlation between MRI findings and neuropathological changes. J Neurol 2011 0.78
79 Autophagy-related proteins (p62, NBR1 and LC3) in intranuclear inclusions in neurodegenerative diseases. Neurosci Lett 2012 0.78
80 Ultrastructural differences in pretangles between Alzheimer disease and corticobasal degeneration revealed by comparative light and electron microscopy. Acta Neuropathol Commun 2014 0.78
81 [An autopsy case of pandemic (H1N1) 2009 influenza virus-associated encephalopathy]. Rinsho Shinkeigaku 2012 0.78
82 ALS-associated protein FIG4 is localized in Pick and Lewy bodies, and also neuronal nuclear inclusions, in polyglutamine and intranuclear inclusion body diseases. Neuropathology 2013 0.78
83 Neuronal and glial tau pathology in early frontotemporal lobar degeneration-tau, Pick's disease subtype. J Neurol Sci 2010 0.77
84 A 65-year-old man with headaches and left homonymous hemianopsia. Neuropathology 2004 0.77
85 Immunohistochemical localization of spatacsin in α-synucleinopathies. Neuropathology 2013 0.77
86 [Epidemiologic study of Creutzfeldt-Jakob disease from autopsy-confirmed cases]. Rinsho Shinkeigaku 2009 0.77
87 Ubiquitin-related proteins in neuronal and glial intranuclear inclusions in intranuclear inclusion body disease. Pathol Int 2012 0.77
88 MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology. Acta Neuropathol 2006 0.77
89 Inclusion-positive cell types in adult-onset intranuclear inclusion body disease: implications for clinical diagnosis. Acta Neuropathol 2008 0.77
90 Reduction of the size of the Golgi apparatus of spinal anterior horn cells in patients with X-linked spinal and bulbar muscular atrophy. Amyotroph Lateral Scler Other Motor Neuron Disord 2003 0.77
91 Myelopathy mimicking subacute combined degeneration in a Down syndrome patient with methotrexate treatment for B lymphoblastic leukemia: report of an autopsy case. Neuropathology 2014 0.77
92 An autopsy case of diffuse neurofibrillary tangles with calcification: early stage pathologic findings. Neuropathology 2009 0.76
93 Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementia. J Neuroinflammation 2013 0.76
94 Distribution of tuft-shaped astrocytes in the cerebral cortex in progressive supranuclear palsy. Acta Neuropathol 2004 0.76
95 Dendritic retraction, but not atrophy, is consistent in amyotrophic lateral sclerosis-comparison between Onuf's neurons and other sacral motor neurons. Acta Neuropathol Commun 2014 0.76
96 [An autopsy case of senile dementia suspected to be influenced by cerebral amyloid angiopathy with multiple cortical microinfarcts]. Rinsho Shinkeigaku 2010 0.76
97 Widespread spinal cord involvement in corticobasal degeneration. Acta Neuropathol 2005 0.76
98 [An autopsied case of progressive supranuclear palsy, initially diagnosed as spinocerebellar degeneration with severe olivopontocerebellar involvement]. Rinsho Shinkeigaku 2011 0.76
99 Gerstmann-Straeussler-Scheinker disease with P102L prion protein gene mutation presenting with rapidly progressive clinical course. Clin Neuropathol 2014 0.76
100 Histologic study of age-related change in the posterior pituitary gland focusing on abnormal deposition of tau protein. Pathol Int 2010 0.76
101 [Cutting-edge MRI techniques for studying neurological diseases focusing on spinocerebellar degeneration]. Rinsho Shinkeigaku 2013 0.75
102 [Decreased myocardial uptake of meta-iodobenzylguanidine in an autopsy-confirmed case of corticobasal degeneration with Lewy bodies restricted to the sympathetic ganglia]. Rinsho Shinkeigaku 2012 0.75
103 Panencephalopathic-type sporadic Creutzfeldt-Jakob disease with circumscribed spongy foci. Clin Neuropathol 2014 0.75
104 [Clinical picture and diagnostic criteria of multiple system atrophy]. Rinsho Shinkeigaku 2014 0.75
105 Neuropathological studies of patients with possible non-herpetic acute limbic encephalitis and so-called acute juvenile female non-herpetic encephalitis. Intern Med 2008 0.75
106 Scopolamine Ointment for Clozapine-Associated Sialorrhea: A Case Report. J Clin Psychopharmacol 2016 0.75
107 [Neuropathology of malignant lymphoma and its related disorders]. Rinsho Shinkeigaku 2002 0.75
108 [An autopsied case of progressive supranuclear palsy presenting with slow progression and unusually prolonged disease duration]. Rinsho Shinkeigaku 2012 0.75
109 [A case of amyloid-β-related cerebral angiitis with ApoE ε4/ε2 genotype]. Rinsho Shinkeigaku 2015 0.75
110 An autopsied case of adult-onset bulbospinalform Alexander disease with a novel S393R mutation in the GFAP gene. Clin Neuropathol 2015 0.75
111 An autopsy case of dementia with Lewy bodies clinically diagnosed to have a behavioral variant of frontotemporal dementia. Clin Neuropathol 2016 0.75
112 [Autopsy findings in a case of dementia with Lewy bodies with marked autonomic failure and repetitive cardiopulmonary arrest]. Rinsho Shinkeigaku 2005 0.75
113 An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease. Neuropathology 2010 0.75
114 Senile onset frontotemporal lobar degeneration with TAR-DNA binding protein 43 proteinopathy primarily presenting with wasteful habits. Psychogeriatrics 2013 0.75
115 [Head injury, no. 2 in series of articles: basic knowledge of neuropathology for neurosurgeons]. No Shinkei Geka 2002 0.75
116 Evaluation of post-application rheological changes in cosmetics using a novel measuring device: relationship to sensory evaluation. J Cosmet Sci 2003 0.75
117 [The diagnosis of neurodegenerative disorders based on clinical and pathological findings using an MRI approach]. Rinsho Shinkeigaku 2011 0.75
118 [Central nervous system neurotoxicity of anticancer chemotherapy]. Nihon Rinsho 2015 0.75
119 [Prion-like protein propagation in neurodegenerative diseases]. Rinsho Shinkeigaku 2012 0.75
120 [Clinicopathologic findings of argyrophilic-grain dementia in a case of mild cognitive impairment converting to dementia]. Rinsho Shinkeigaku 2012 0.75
121 [TDP-43 proteinopathies, toward understanding of the molecular pathogenesis]. Rinsho Shinkeigaku 2009 0.75
122 [A case of cerebral amyloid angiopathy with reversible white matter lesions and multiple cerebral microbleeds]. Rinsho Shinkeigaku 2012 0.75
123 Sporadic adult-onset neuronal intranuclear inclusion disease with the main presentation of repeated cerebellar ataxia: a case study. Rinsho Shinkeigaku 2016 0.75
124 Neuropathological investigation of regions responsible for semantic aphasia in frontotemporal lobar degeneration. Dement Geriatr Cogn Disord 2009 0.75
125 [An autopsy case of purulent meningitis, presenting high signals in subarachnoid space and ventricles in diffusion weighted images (DWIs)]. Rinsho Shinkeigaku 2003 0.75
126 [Frontotemporal dementia (FTD) and genetic mutations including progranulin gene]. Rinsho Shinkeigaku 2008 0.75
127 Expanding concept of clinical conditions and symptoms in multiple system atrophy. Rinsho Shinkeigaku 2016 0.75
128 Pathological background of subcortical hyperintensities on diffusion-weighted images in a case of neuronal intranuclear inclusion disease. Clin Neuropathol 2016 0.75
129 [An autopsy case of progressive multifocal leukoencephalopathy: comparison of magnetic resonance imaging findings with the pathological findings]. Brain Nerve 2011 0.75
130 [An autopsied case of dementia with lewy bodies presenting with hemispheric cerebral cortical atrophy with selective neuronal necrosis after status epilepticus]. Brain Nerve 2012 0.75
131 MM2-cortical-type sporadic Creutzfeldt-Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course. Neuropathology 2008 0.75
132 [An autopsied case of dentato-rubro-pallido-luysian atrophy with atypical pathological lesions]. No To Shinkei 2002 0.75
133 [An Autopsy Case of Globular Glial Tauopathy Presenting with Amyotrophic Lateral Sclerosis with Dementia]. Brain Nerve 2016 0.75
134 [Significance of the TDP-43 deposition in FTLD-U and ALS]. Rinsho Shinkeigaku 2008 0.75
135 [An autopsied case of argyrophilic grain dementia with parkinsonism due to multiple lacunar infarctions]. Brain Nerve 2013 0.75
136 Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement. Neuropathology 2006 0.75
137 [Autopsy case of Lissauer's general paresis with rapidly progressive left hemiparesis]. Rinsho Shinkeigaku 2009 0.75
138 [An autopsy case of long-course multiple system atrophy (MSA) with remarkable atrophy and numerous NCI in the temporal lobe]. No To Shinkei 2006 0.75
139 An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein. Neuropathology 2013 0.75
140 [An autopsied case of senile onset frontotemporal lobar degeneration]. Rinsho Shinkeigaku 2011 0.75
141 Definition and differentials: how to distinguish disease-specific changes on microscopy. Neuropathology 2014 0.75
142 Multiple findings in elderly adults with confirmed Alzheimer's disease. J Am Geriatr Soc 2012 0.75