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Research Output 1985 2020

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Letter
2020
1 Citation (Scopus)

A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy

Sasaki, R., Ohta, Y., Hatanaka, N., Tadokoro, K., Nomura, E., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Omote, Y., Morimoto, E., Teshigawara, S., Wada, J., Goto, Y. I. & Abe, K., Jan 15 2020, In : Journal of the neurological sciences. 408, 116460.

Research output: Contribution to journalLetter

MELAS Syndrome
Temporal Lobe
Mitochondrial DNA
Atrophy
Mutation
2019
1 Citation (Scopus)

A unique Japanese CPEO family with a novel homozygous m.14819 T > G (p. S25A) substitution

Nomura, E., Ohta, Y., Tadokoro, K., Sato, K., Sasaki, R., Takahashi, Y., Yamashita, T., Takemoto, M., Hishikawa, N., Goto, Y. I. & Abe, K., May 15 2019, In : Journal of the neurological sciences. 400, p. 145-147 3 p.

Research output: Contribution to journalLetter

Chronic Progressive External Ophthalmoplegia
Mitochondrial DNA
2018

A mild myopathy with anti-SRP plus anti-PL-12 antibodies successfully treated by oral steroid monotherapy

Tadokoro, K., Ohta, Y., Sasaki, R., Takahashi, Y., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Hayashi, K., Morishita, M., Nishino, I. & Abe, K., May 15 2018, In : Journal of the Neurological Sciences. 388, p. 7-9 3 p.

Research output: Contribution to journalLetter

Signal Recognition Particle
Muscular Diseases
Steroids
Antibodies

A new familial distal myopathy in Japan with predominant upper extremities

Takahashi, Y., Ohta, Y., Sasaki, R., Tadokoro, K., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Nishino, I. & Abe, K., Jul 15 2018, In : Journal of the Neurological Sciences. 390, p. 205-207 3 p.

Research output: Contribution to journalLetter

Distal Myopathies
Upper Extremity
Japan

A novel presenilin 1 mutation (Leu418Trp) associated with spasticity, parkinsonism, and white matter lesion in a dominant Alzheimer's family

Takahashi, Y., Ohta, Y., Sasaki, R., Tadokoro, K., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Haraguchi, T., Ikeuchi, T. & Abe, K., Apr 15 2018, In : Journal of the Neurological Sciences. 387, p. 166-169 4 p.

Research output: Contribution to journalLetter

Presenilin-1
Parkinsonian Disorders
Alzheimer Disease
Mutation
White Matter

Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation

Tadokoro, K., Ohta, Y., Sasaki, R., Takahashi, Y., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Nakamura, K., Nishino, I. & Abe, K., Oct 15 2018, In : Journal of the Neurological Sciences. 393, p. 142-144 3 p.

Research output: Contribution to journalLetter

Congenital Structural Myopathies
Dilated Cardiomyopathy
Mutation

Two cases of late onset familial amyloid polyneuropathy with a Glu61Lys transthyretin variant

Nakano, Y., Tadokoro, K., Ohta, Y., Sato, K., Takemoto, M., Hishikawa, N., Yamashita, T., Yamashita, T., Ando, Y. & Abe, K., Jul 15 2018, In : Journal of the Neurological Sciences. 390, p. 22-25 4 p.

Research output: Contribution to journalLetter

Familial Amyloid Neuropathies
Prealbumin
2017
3 Citations (Scopus)

A case of very long longitudinally extensive transverse myelitis (LETM) with necrotizing Vasculitis

Sato, K., Tsunoda, K., Yamashita, T., Takemoto, M., Hishikawa, N., Ohta, Y., Takahashi, T., Nakashima, I., Yasuhara, T., Date, I. & Abe, K., Feb 15 2017, In : Journal of the Neurological Sciences. 373, p. 152-154 3 p.

Research output: Contribution to journalLetter

Transverse Myelitis
Neuromyelitis Optica
Vasculitis
Spinal Cord
Differential Diagnosis

An AOA2 patient with a novel compound heterozygous SETX frame shift mutations

Motokura, E., Yamashita, T., Takahashi, Y., Tsunoda, K., Sato, K., Takemoto, M., Hishikawa, N., Ohta, Y., Hashiguchi, A., Takashima, H. & Abe, K., Jan 15 2017, In : Journal of the Neurological Sciences. 372, p. 294-296 3 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)

A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene

Tsunoda, K., Yamashita, T., Motokura, E., Takahashi, Y., Sato, K., Takemoto, M., Hishikawa, N., Ohta, Y., Nishikawa, A., Nishino, I. & Abe, K., Feb 15 2017, In : Journal of the Neurological Sciences. 373, p. 254-257 4 p.

Research output: Contribution to journalLetter

Nemaline Myopathies
Muscle Proteins
Muscle Weakness
Heterozygote
Respiratory Insufficiency
2 Citations (Scopus)

Marked hypertriglyceridemia induced by interferon-β1a therapy in a clinically isolated syndrome patient

Kawahara, Y., Yamashita, T., Ohta, Y., Sato, K., Tsunoda, K., Takemoto, M., Hishikawa, N., Eguchi, J. & Abe, K., Feb 15 2017, In : Journal of the Neurological Sciences. 373, p. 144-146 3 p.

Research output: Contribution to journalLetter

Immunologic Adjuvants
Chylomicrons
Lipoprotein Lipase
Hypertriglyceridemia
Interferon-beta
2016
2 Citations (Scopus)

An autopsy case of intravascular large B-cell lymphoma with subcortical U-fiber sparing and unique lymphocyte markers

Sato, K., Motokura, E., Deguchi, K., Takemoto, M., Hishikawa, N., Ohta, Y., Yamashita, T., Itakura, J. & Abe, K., Oct 15 2016, In : Journal of the Neurological Sciences. 369, p. 273-275 3 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)

Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

Sato, K., Yamashita, T., Hatanaka, N., Takemoto, M., Hishikawa, N., Ohta, Y. & Abe, K., Sep 15 2016, In : Journal of the Neurological Sciences. 368, p. 147-149 3 p.

Research output: Contribution to journalLetter

Ubiquitin-Protein Ligases
Parkinson Disease
Differential Diagnosis
Phenotype
Mutation