Y. Fujita

发表

Anti-MuSK Antibody-positive Myasthenia Gravis Mimicking Amyotrophic Lateral Sclerosis.

K. Okamoto, M. Ikeda, M. Motomura, 2015, Internal medicine.

An autopsy case of familial amyotrophic lateral sclerosis with a TARDBP Q343R mutation

M. Hasegawa, K. Okamoto, M. Takatama, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

Reduced expression of BTBD10 in anterior horn cells with Golgi fragmentation and pTDP‐43‐positive inclusions in patients with sporadic amyotrophic lateral sclerosis

K. Okamoto, M. Takatama, M. Ikeda, 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

[Case of recurrent delayed radiation myelopathy with 5-year remission interval].

K. Okamoto, M. Ikeda, S. Tsukagoshi, 2010, Rinsho shinkeigaku = Clinical neurology.

The Golgi apparatus is fragmented in spinal cord motor neurons of amyotrophic lateral sclerosis with basophilic inclusions

N. Gonatas, K. Okamoto, H. Kusaka, 2002, Acta Neuropathologica.

Prolonged distal latency of the median motor nerve is associated with poor prognosis in amyotrophic lateral sclerosis

Y. Ikeda, K. Nagashima, Y. Fujita, 2020, Neurological research.

Pathology of protein synthesis and degradation systems in ALS

K. Okamoto, Y. Fujita, Y. Mizuno, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

Encephalopathy with amyloid angiopathy and numerous amyloid plaques with low levels of CSF Aβ1–40/Aβ1–42

K. Okamoto, M. Amari, M. Takatama, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report

E. Matsubara, M. Shoji, K. Okamoto, 2010, Journal of the Neurological Sciences.

Fragmentation of the Golgi apparatus of the anterior horn cells in patients with familial amyotrophic lateral sclerosis with SOD1 mutations and posterior column involvement

N. Gonatas, K. Okamoto, A. Hirano, 2000, Journal of the Neurological Sciences.

Cytoplasmic TDP‐43 accumulation in cells of the adrenal medulla in individuals with or without amyotrophic lateral sclerosis

K. Okamoto, M. Amari, M. Takatama, 2014, Neuropathology : official journal of the Japanese Society of Neuropathology.

Bunina bodies in amyotrophic lateral sclerosis

K. Okamoto, Y. Fujita, Y. Mizuno, 1993, Neuropathology : official journal of the Japanese Society of Neuropathology.

Anterior horn cells with abnormal TDP-43 immunoreactivities show fragmentation of the Golgi apparatus in ALS

K. Okamoto, M. Takatama, Y. Fujita, 2008, Journal of the Neurological Sciences.

Fragmentation of the Golgi apparatus of the ballooned neurons in patients with corticobasal degeneration and Creutzfeldt-Jakob disease

N. Gonatas, K. Okamoto, K. Wakabayashi, 2000, Acta Neuropathologica.

Peripherin partially localizes in Bunina bodies in amyotrophic lateral sclerosis

K. Okamoto, M. Takatama, Y. Fujita, 2011, Journal of the Neurological Sciences.

Anti-Hu Antibody-associated Paraneoplastic Neurological Syndrome Showing Peripheral Neuropathy and Atypical Multifocal Brain Lesions.

M. Kurabayashi, K. Makioka, Y. Ikeda, 2015, Internal medicine.

Morphological differences of intraneuronal ubiquitin‐positive inclusions in the dentate gyrus and parahippocampal gyrus of motor neuron disease with dementia

S. Al-Sarraj, P. Leigh, K. Okamoto, 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.

[A case of filamentous fungal infection showing tumor-like expansion in the cisterns].

Y. Ikeda, Y. Tsutsumi, S. Tsukagoshi, 2014, Rinshō shinkeigaku Clinical neurology.

Morphological changes of Golgi apparatus in adult rats after facial nerve injuries

K. Okamoto, K. Ikeda, K. Watabe, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

Optineurin in neurodegenerative diseases

K. Okamoto, M. Takatama, Y. Nakazato, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

Numerous FUS‐positive inclusions in an elderly woman with motor neuron disease

K. Okamoto, M. Takatama, M. Ikeda, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation

M. Ikeda, Y. Senoo, Y. Fujita, 2011, Neurology.

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.

A middle-aged male suffering from encephalopathy with cerebral amyloid angiopathy (CAA) with amyloid beta (Aβ) presented with initial symptoms of transient consciousness disturbance and left visual field photophobia. Lesions with aberrantly high signal on T2-weighted magnetic resonance imaging (MRI)

K. Okamoto, M. Amari, M. Takatama, 2012 .

[Reversible posterior leukoencephalopathy syndrome associated with carbamazepine-induced hypertension].

K. Okamoto, M. Ikeda, N. Furuta, 2009, Rinsho shinkeigaku = Clinical neurology.

Sibling Cases of Charcot-Marie-Tooth Disease Type 4H with a Homozygous FGD4 Mutation and Cauda Equina Thickening

Y. Ikeda, H. Takashima, K. Nagashima, 2021, Internal medicine.

Cerebrospinal fluid levels of phosphorylated tau and Aβ1-38/Aβ1-40/Aβ1-42 in Alzheimer’s disease with PS1 mutations

K. Okamoto, M. Amari, M. Takatama, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Pathology of the inferior olivary nucleus in patients with multiple system atrophy

Yoichi Nakazato, Yukio Fujita, Koichi Okamoto, 2002, Acta Neuropathologica.

The involvement of the neuronal Golgi apparatus and trans-Golgi network in the human olivary hypertrophy

N. Gonatas, K. Okamoto, M. Takatama, 2000, Journal of the Neurological Sciences.

Fragmentation of Golgi apparatus of nigral neurons with α-synuclein-positive inclusions in patients with Parkinson’s disease

Yukio Fujita, Eisaku Ohama, Koichi Okamoto, 2006, Acta Neuropathologica.

Bilateral striatal necrosis caused by a founder mitochondrial 14459G>A mutation in two independent Japanese families

K. Makioka, Y. Ikeda, H. Takashima, 2017, Journal of the Neurological Sciences.

Clinical, radiological, and molecular analyses of neuronal intranuclear inclusion disease with polyglycine inclusions

Y. Ikeda, Minori Furuta, S. Tsukagoshi, 2023, Journal of the Neurological Sciences.

Phosphorylation-dependent TDP-43 antibody detects intraneuronal dot-like structures showing morphological characters of granulovacuolar degeneration

C. Lemere, K. Okamoto, M. Takatama, 2009, Neuroscience Letters.

Cerebral Microbleeds, Cerebrospinal Fluid, and Neuroimaging Markers in Clinical Subtypes of Alzheimer's Disease

K. Ishii, N. Hattori, Y. Tsushima, 2021, Frontiers in Neurology.

Involvement of endoplasmic reticulum stress defined by activated unfolded protein response in multiple system atrophy

K. Okamoto, M. Takatama, K. Makioka, 2010, Journal of the Neurological Sciences.

Neurogenic calf amyotrophy with CK elevation by entrapment radiculopathy; clinical, radiological, and pathological analyses of 18 cases

M. Ikeda, K. Makioka, Y. Ikeda, 2020, Journal of Neurology.

Parkinson's disease presenting with oculogyric crisis in the off period.

K. Okamoto, K. Makioka, Minori Furuta, 2014, Internal medicine.

Progressive Pseudolithiasis Associated with the Intravenous Administration of Ceftriaxone in Patients with Central Nervous System Infections

K. Makioka, Y. Ikeda, Kunihiko Ishizawa, 2017, Internal medicine.

Anti-LRP4 Antibody-associated Myasthenia Gravis with a Rare Complication of Thymoma Successfully Treated by Thymectomy

K. Makioka, Y. Ikeda, O. Higuchi, 2020, Internal medicine.

Increased Neurofilament Light Chain and YKL-40 CSF Levels in One Japanese IBMPFD Patient With VCP R155C Mutation: A Clinical Case Report With CSF Biomarker Analyses

Y. Tsushima, T. Higuchi, M. Ikeda, 2020, Frontiers in Neurology.

Novel GBE1 mutation in a Japanese family with adult polyglucosan body disease

T. Matsukawa, S. Tsuji, S. Morishita, 2017, Neurology: Genetics.

Golgi apparatus of the motor neurons in patients with amyotrophic lateral sclerosis and in mice models of amyotrophic lateral sclerosis

Yukio Fujita, Koichi Okamoto, K. Okamoto, 2005, Neuropathology : official journal of the Japanese Society of Neuropathology.

A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits.

K. Okamoto, M. Ikeda, M. Amanuma, 2012, Internal medicine.

Differential and quantitative neuroimaging characteristics of inclusion body myositis

Y. Tsushima, Y. Ikeda, Minori Furuta, 2019, Journal of Clinical Neuroscience.

Comparison of phosphorylated TDP-43-positive inclusions in oculomotor neurons in patients with non-ALS and ALS disorders

K. Okamoto, M. Takatama, Y. Fujita, 2012, Journal of the Neurological Sciences.

CSF levels of Aβ1-38/Aβ1-40/Aβ1-42 and 11C PiB-PET studies in three clinical variants of primary progressive aphasia and Alzheimer’s disease

Y. Tsushima, K. Okamoto, M. Amari, 2014, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Deep White Matter Lesions Are Associated with Early Recognition of Dementia in Alzheimer's Disease.

Y. Tsushima, T. Higuchi, M. Ikeda, 2019, Journal of Alzheimer's disease : JAD.

Changes in the clinical features of amyotrophic lateral sclerosis in rural Japan.

K. Okamoto, K. Makioka, N. Furuta, 2013, Internal medicine.

An analysis of prognostic factors after percutaneous endoscopic gastrostomy placement in Japanese patients with amyotrophic lateral sclerosis

M. Ikeda, K. Makioka, Y. Ikeda, 2017, Journal of the Neurological Sciences.

P3-019: Diverse neurological symptoms presenting severe dementia, psychiatric Symptoms and motor deficits in early-onset familial Alzheimer's disease

K. Okamoto, K. Ishiguro, M. Ikeda, 2008, Alzheimer's & Dementia.

Hypersialylation is a common feature of neurofibrillary tangles and granulovacuolar degenerations in Alzheimer's disease and tauopathy brains

K. Okamoto, M. Takatama, M. Ikeda, 2016, Neuropathology : official journal of the Japanese Society of Neuropathology.

Fragmentation of the Golgi apparatus of Betz cells in patients with amyotrophic lateral sclerosis

N. Gonatas, K. Okamoto, M. Amari, 1999, Journal of the Neurological Sciences.