T. Ibi

发表

MM1‐type sporadic Creutzfeldt‐Jakob disease with unusually prolonged disease duration presenting with panencephalopathic‐type pathology

Mari Yoshida, Y. Hashizume, T. Kitamoto, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

Therapeutic potential of pyruvate therapy for mitochondrial diseases.

N. Fuku, Masashi Tanaka, Y. Nishigaki, 2007, Mitochondrion.

Open-label trial and randomized, double-blind, placebo-controlled, crossover trial of hydrogen-enriched water for mitochondrial and inflammatory myopathies

K. Ohno, Mikako Ito, Masafumi Ito, 2011, Medical gas research.

LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinity

K. Ohno, Y. Yamashita, T. Matsuura, 2014, Neurobiology of Disease.

Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomach.

T. Azuma, M. Ohtani, M. Yoneda, 2004, Internal medicine.

Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy.

K. Ohno, T. Ozawa, K. Sahashi, 1992, Gerontology.

Progressive external ophthalmoplegia and myositis.

Tanaka, K. Ohno, T. Mitsuma, 1993, Internal medicine.

Immunohistochemical demonstration of carbonic anhydrase III and muscle-specific enolase in paraffin-embedded human skeletal muscle sections

H. Nagura, K. Kato, H. Haimoto, 2004, Acta Neuropathologica.

Immunohistochemical demonstration of β‐enolase in human skeletal muscle

Kanefusa Kato, I. Sobue, K. Sahashi, 1983 .

Dysferlin mutations in Japanese Miyoshi myopathy

Y. Itoyama, I. Nonaka, Kayoko Saito, 2003, Neurology.

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.

Y. Akao, K. Ozawa, M. Naoi, 2002, Journal of biomedical science.

(R) salsolinol N‐methyltransferase activity increases in parkinsonian lymphocytes

M. Naoi, W. Maruyama, M. Benedetti, 1998, Annals of neurology.

Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B

Y. Itoyama, S. Tsuji, G. Sobue, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2 B

Y. Itoyama, S. Tsuji, G. Sobue, 2012 .

Autosomal Dominant Hyaline Body Myopathy Presenting As Scapuloperoneal Syndrome

Y. Narita, A. Taniguchi, S. Kuzuhara, 1997, Neurology.

Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies.

K. Arahata, H. Sugita, K. Sahashi, 1994, Internal medicine.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

T. Ozawa, Masashi Tanaka, Tomoko Yamamoto, 1991, Annals of neurology.

Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome.

K. Ohno, T. Ozawa, H. Ino, 1991, Biochimica et biophysica acta.

FGF-20, a novel neurotrophic factor, preferentially expressed in the substantia nigra pars compacta of rat brain.

A. Akaike, N. Itoh, Y. Watanabe, 2000, Biochemical and biophysical research communications.

Acute predominantly sensory neuropathy

T. Matsui, K. Sahashi, T. Ibi, 1985, Klinische Wochenschrift.

A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis

S. Sakoda, H. Mochizuki, M. Takahashi, 2012, Neuroscience Letters.

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy

O. Onodera, S. Tsuji, Y. Ishikawa, 1992, Neurology.

[Immunohistochemical localization of chymase; a mast cell marker and clinical significance in diseased human skeletal muscle].

K. Sahashi, T. Ibi, G. Zhang, 1997, Rinshō shinkeigaku Clinical neurology.

[Immunostaining of anti-Bcl-2 antibody in diseased human muscles].

T. Mitsuma, K. Sahashi, T. Ibi, 1996, Rinsho shinkeigaku = Clinical neurology.

Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy

A. Masuda, Jun Shinmi, K. Ohno, 2012, Journal of Human Genetics.

Multiplicity of abnormal dystrophin in Becker muscular dystrophy A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin

I. Nonaka, Teruo Shimizu, K. Sahashi, 1994, Journal of the Neurological Sciences.

Clinical and neuropathological features of a neurodegenerative disorder in the central nervous system with progressive head drooping (Kubisagari)

Y. Hashizume, N. Nakao, K. Sahashi, 2004, Acta Neuropathologica.

Pathogenesis and clinical features of rhabdomyolysis

K. Sahashi, T. Ibi, 2009 .

Functional characterisation of mitochondrial tRNATyrmutation (5877G→A) associated with familial chronic progressive external ophthalmoplegia

K. Ohno, Masashi Tanaka, K. Sahashi, 2001, Journal of medical genetics.

Gene Therapy for Mitochondrial Disease by Delivering Restriction Endonuclease SmaI into Mitochondria

Y. Akao, K. Ozawa, M. Naoi, 2002, Journal of Biomedical Science.

[Clinical analyses on moving toes in "painful legs and moving toes"].

T. Mano, S. Iwase, K. Sahashi, 1989, Rinshō shinkeigaku Clinical neurology.

Cytoplasmic body and mitochondrial DNA deletion

K. Ohno, T. Ozawa, Masashi Tanaka, 1990, Journal of the Neurological Sciences.

[A case of myasthenia gravis following sarcoidosis and Hashimoto's thyroiditis].

K. Sahashi, N. Nakao, H. Nishida, 2000, Rinsho shinkeigaku = Clinical neurology.

[A mother and her son with autosomal dominant bulbar spinal muscular atrophy].

S. Tsuji, K. Sahashi, S. Igarashi, 1992, Rinsho shinkeigaku = Clinical neurology.

Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations.

S. Dimauro, C. Liou, T. Fujii, 2010, Mitochondrion.

[A case of a mitochondrial myopathy with cylindrical spirals (author's transl)].

G. Sobue, K. Sahashi, H. Yamamoto, 1982, Rinsho shinkeigaku = Clinical neurology.

[Clinical features of the peripheral nerve involvement in necrotizing angitis--characteristics in polyarteritis nodosa and allergic granulomatous angitis].

G. Sobue, T. Mitsuma, Y. Matsuoka, 1989, Rinshō shinkeigaku Clinical neurology.

[Dyskinesia-hyperpyrexia syndrome in a patient with Parkinson's disease: a case report].

M. Doyu, J. Niwa, T. Ibi, 2015, Rinsho shinkeigaku = Clinical neurology.

[Immunostaining of anti-Fas IgG1 antibody in diseased human muscle].

K. Sahashi, J. Ling, T. Ibi, 1995, Rinsho shinkeigaku = Clinical neurology.

[HTLV-I associated myelopathy (HAM) and sarcoid myopathy].

T. Mitsuma, K. Sahashi, T. Ibi, 1991, Rinshō shinkeigaku Clinical neurology.

[A case of LGMD2A identified with both western blot analysis and immunostaining of calpain 3 in biopsied muscle].

K. Sahashi, N. Nakao, T. Ibi, 2000, Rinsho shinkeigaku = Clinical neurology.