A. Mitsutake

发表

Severe pleuritis and pericarditis associated with very‐late‐onset systemic lupus erythematosus

Y. Shiio, Tatsuya Sato, T. Hideyama, 2018, Journal of general and family medicine.

CSF p-tau181 increases in patients with neuronal intranuclear inclusion disease without amyloid burden

A. Tokumaru, S. Murayama, H. Ishiura, 2022, medRxiv.

Corticobasal degeneration with deep white matter lesion diagnosed by brain biopsy

M. Hasegawa, Y. Shiio, Tatsuya Sato, 2020, Neuropathology : official journal of the Japanese Society of Neuropathology.

Rupture of a medial striate artery aneurysm associated with spontaneous middle cerebral artery stenosis

Y. Shiio, S. Kure, Tatsuya Sato, 2017 .

TDP‐43 Proteinopathy Presenting with Typical Symptoms of Parkinson's Disease

M. Hasegawa, H. Ishiura, H. Mochizuki, 2022, Movement Disorders.

Pneumococcal meningitis with vertebral osteomyelitis, iliopsoas abscess, and infected abdominal aortic aneurysm

H. Matsumoto, M. Ikemura, K. Hoshina, 2018 .

A central nervous system metastasis of melanoma with stroke‐like onset of left‐lower quadrantanopsia

Y. Shiio, M. Ohno, Y. Narita, 2020, Journal of general and family medicine.

Clinical and neuroimaging review of triplet repeat diseases

Y. Nakata, O. Abe, T. Moritani, 2022, Japanese Journal of Radiology.

The first Japanese case of biopsy‐confirmed small‐fiber neuropathy related to celiac disease

Y. Shiio, Y. Ando, Tatsuya Sato, 2018, Neurology and Clinical Neuroscience.

A Japanese family with primary familial brain calcification presenting with paroxysmal kinesigenic dyskinesia - A comprehensive mutational analysis-

T. Matsukawa, S. Tsuji, Y. Shiio, 2020, Journal of the Neurological Sciences.

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Shinichi Morishita, Yasuo Terao, Yuko Saito, 2019, Nature Genetics.

Paraspinal muscle involvement in herpes zoster-induced abdominal wall pseudohernia revealed by electrophysiological and radiological studies

Y. Shiio, Takuya Sasaki, Tatsuya Sato, 2017, Journal of the Neurological Sciences.

Isolated Paravermal Hyperintensities in Neuronal Intranuclear Inclusion Disease

C. Fujimoto, H. Ishiura, F. Suzuki, 2022, Neurology.

Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene

S. Tsuji, K. Tsunoda, H. Sawamura, 2020, Investigative ophthalmology & visual science.

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

T. Matsukawa, S. Tsuji, Jun Shinmi, 2019, Nature Genetics.

[A case of intravascular large B-cell lymphoma that presented with recurrent multiple cerebral infarctions and followed an indolent course].

K. Kuriki, N. Sakai, A. Mitsutake, 2015, Rinsho shinkeigaku = Clinical neurology.

Intramedullary hemorrhage with multiple cavernous angiomas in the brain

Isao Ono, J. Hanakita, Toshiyuki Takahashi, 2017 .

CSF P-Tau181 and Other Biomarkers in Patients With Neuronal Intranuclear Inclusion Disease

A. Tokumaru, S. Murayama, H. Ishiura, 2022, Neurology.

A case of Parkinson's disease following autoimmune autonomic ganglionopathy

H. Matsumoto, S. Nakane, O. Higuchi, 2019, Neurology and Clinical Neuroscience.

Lenalidomide-Induced Ischemic Cerebrovascular Disease in Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes Syndrome.

H. Matsumoto, N. Tsukada, H. Hashida, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Tumefactive multiple sclerosis which initially presented with brainstem encephalitis with a long-term follow-up.

Y. Shiio, Tatsuya Sato, J. Shimizu, 2019, Multiple sclerosis and related disorders.

Elderly‐onset case of hereditary neuropathy with liability to pressure palsies: A case report

Y. Shiio, Tatsuya Sato, T. Hideyama, 2018, Neurology and Clinical Neuroscience.

Diagnostic Values of Venous Peak Lactate, Lactate-to-pyruvate Ratio, and Fold Increase in Lactate from Baseline in Aerobic Exercise Tests in Patients with Mitochondrial Diseases

Kenichiro Sato, Toshihiro Hayashi, K. Murayama, 2021, Internal medicine.

A case of late‐onset Krabbe disease which showed subacute progression of spastic paresis with bilateral spinal cord lesions

T. Matsukawa, S. Tsuji, Y. Terao, 2018, Neurology and Clinical Neuroscience.

Severe dilated cardiomyopathy and ventricular arrhythmia in a patient with Emery‐Dreifuss muscular dystrophy harboring a novel frameshift mutation in EMD

H. Ishiura, J. Shimizu, K. Sakuishi, 2021, Neurology and Clinical Neuroscience.

Toxic Epidermal Necrolysis in a Patient with Autoimmune Limbic Encephalitis with Anti-Glutamate Receptor Antibodies

H. Matsumoto, Junko Yoshimura, S. Imakado, 2018, Case Reports in Neurology.

Paracentral homonymous hemianopic scotoma caused by anterior choroidal artery infarction.

H. Sawamura, Y. Nagashima, A. Mitsutake, 2021, QJM : monthly journal of the Association of Physicians.

Sjögren syndrome combined with myositis which is pathologically compatible with inclusion body myositis

I. Nishino, Y. Shiio, Tatsuya Sato, 2020 .

The Myocardial Accumulation of Aggregated Desmin Protein in a Case of Desminopathy with a de novo DES p.R406W Mutation.

M. Ono, S. Morishita, Yukako Shintani-Domoto, 2023, Internal medicine.

Favorable outcome of hematopoietic stem cell transplantation in late-onset Krabbe disease

T. Matsukawa, H. Mori, M. Kurokawa, 2023, Brain and Development.