M. Kunishige

发表

Clinical, pathological, and genetic features of limb‐girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families

J. Beckmann, T. Fujiwara, I. Richard, 1998, Muscle & nerve.

Lysosomal enzyme activities in skeletal muscle of patients with neuromuscular diseases

S. Kashiwagi, H. Kawai, M. Kunishige, 1995, Muscle & nerve.

Expanding Phenotype and Clinical Heterogeneity in Patients with Identical Mutation of the Parkin Gene

S. Yoshida, T. Mitsui, Y. Kuroda, 2004, European Neurology.

Beneficial Effect of Steroid Pulse Therapy on Acute Viral Encephalitis

T. Mitsui, M. Kunishige, R. Yamasaki, 2003, European Neurology.

Dermatomyositis with peripheral nervous system involvement: activation of vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) in vasculitic lesions.

I. Endo, T. Mitsui, N. Matsui, 2003, Internal medicine.

Localization and amount of myoglobin and myoglobin mRNA in ragged‐red fiber of patients with mitochondrial encephalomyopathy

T. Mitsui, M. Akaike, M. Shono, 1996, Muscle & nerve.

Oxidative stress–associated mitochondrial dysfunction in corticosteroid‐treated muscle cells

T. Mitsui, Toshio Matsumoto, Y. Kuroda, 2004, Muscle & nerve.

Central motor conduction in patients with anti-ganglioside antibody associated neuropathy syndromes and hyperreflexia

I. Endo, T. Mitsui, H. Yoshino, 2002, Journal of neurology, neurosurgery, and psychiatry.

Dissociation between titer of anti-ganglioside antibody and severity of symptoms in a case of Guillain–Barré syndrome with treatment-related fluctuation

S. Yoshida, T. Mitsui, Toshio Matsumoto, 2003, Journal of the Neurological Sciences.

Short communication Dissociation between titer of anti-ganglioside antibody and severity of symptoms in a case of Guillain-Barresyndrome with treatment-related fluctuation

S. Yoshida, T. Mitsui, Toshio Matsumoto, 2003 .

Complicated paraneoplastic neurological syndromes: a report of two patients with small cell or non-small cell lung cancer

I. Endo, T. Mitsui, Toshio Matsumoto, 2003, Clinical Neurology and Neurosurgery.

Graves' disease in HTLV-I carriers

M. Akaike, M. Abe, H. Kawai, 1995, Journal of Molecular Medicine.

Guillain-Barré syndrome and hemophagocytic lymphohistiocytosis in a patient with severe chronic active Epstein–Barr virus infection syndrome

T. Mitsui, Toshio Matsumoto, H. Yoshino, 2005, Clinical Neurology and Neurosurgery.

Isolated cranial neuropathy associated with anti-glycolipid antibodies

I. Endo, T. Mitsui, Toshio Matsumoto, 2004, Journal of the Neurological Sciences.

Functional association between nicotinic acetylcholine receptor and sarcomeric proteins via actin and desmin filaments

T. Mitsui, M. Akaike, T. Endo, 2000, Journal of cellular biochemistry.

Preferential Subsarcolemmal Localization of Dystrophin and β‐dystroglycan mRNA in Human Skeletal Muscles

T. Mitsui, H. Kawai, M. Kunishige, 1997, Journal of neuropathology and experimental neurology.

Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies

T. Mitsui, M. Nagasawa, M. Akaike, 1996, Journal of the Neurological Sciences.

Severe dermatomyositis with rhabdomyolysis and paralytic ileus: a case successfully treated with plasmapheresis and intravenous immunoglobulin

I. Endo, T. Mitsui, Y. Kuroda, 2002, European Journal of Neurology.

Successful treatment with tacrolimus in a case of refractory dermatomyositis.

T. Mitsui, Toshio Matsumoto, Y. Kuroda, 2005, Internal medicine.

Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue‐specific time courses of mutation frequency but similar mutation types

S. Sommer, K. Hill, J. Longmate, 2004, Environmental and molecular mutagenesis.

Parkin enhances mitochondrial biogenesis in proliferating cells.

T. Mitsui, H. Azuma, M. Akaike, 2006, Human molecular genetics.

Preferential gray matter involvement in dengue myelitis

I. Kurane, T. Mitsui, B. Tan, 2004, Neurology.

Parkin affects mitochondrial function and apoptosis in neuronal and myogenic cells.

T. Mitsui, Toshio Matsumoto, Y. Kuroda, 2006, Biochemical and biophysical research communications.

Mitochondrial encephalomyopathy with autosomal dominant inheritance: A clinical and genetic entity of mitochondrial diseases

M. Akaike, H. Kawai, M. Kunishige, 1995, Muscle & nerve.

Cardiac dysfunction in patients with chronic progressive external ophthalmoplegia

H. Kawai, Masashi Akaike, M. Kunishige, 1994, Clinical cardiology.

Spontaneous mutation frequency and pattern in Big Blue® mice fed a vitamin E‐supplemented diet

S. Sommer, K. Hill, A. Halangoda, 1999, Environmental and molecular mutagenesis.

Neuro-Behçet’s disease with chorea after remission of intestinal Behçet’s disease

T. Mitsui, M. Kunishige, H. Nakahira, 2004, Clinical Rheumatology.

Delayed Vasospasm in Late Postpartum Cerebral Angiopathy after Withdrawal of Methylergometrine

T. Mitsui, M. Kunishige, R. Kuriwaka, 2002, Cerebrovascular Diseases.

Central motor conduction in cervical dystonia with cervical spondylotic myelopathy

T. Mitsui, Toshio Matsumoto, M. Kunishige, 2005, Clinical Neurology and Neurosurgery.

Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice.

T. Mitsui, H. Kawai, M. Kunishige, 1996, Biochemical and biophysical research communications.

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1997, Journal of the Neurological Sciences.

Interferon Alpha-2a Therapy for Disseminated Intravascular Coagulation in a Patient with Blue Rubber Bleb Nevus Syndrome

H. Azuma, Y. Arii, H. Kawai, 1997, Angiology.

Anti-neuronal antibodies in acute pandysautonomia.

R. Kaji, T. Mitsui, Toshio Matsumoto, 2010, Internal medicine.

Involvement of mitochondria in myasthenia gravis complicated with dermatomyositis and rheumatoid arthritis: a case report

T. Mitsui, Toshio Matsumoto, Y. Kuroda, 2005, Acta Neuropathologica.

Heterogeneous Muscular Involvement in Inclusion Body Myositis

R. Kaji, T. Mitsui, Y. Kuroda, 2010 .

Mutation frequency is reduced in the cerebellum of Big Blue mice overexpressing a human wild type SOD1 gene.

S. Sommer, K. Hill, K. Farwell, 2001, Mutation research.

Beneficial Effect of Tacrolimus on Myasthenia Gravis With Thymoma

I. Endo, T. Mitsui, Toshio Matsumoto, 2007, The neurologist.

Overexpressions of myoglobin and antioxidant enzymes in ragged‐red fibers of skeletal muscle from patients with mitochondrial encephalomyopathy

T. Mitsui, M. Akaike, Toshio Matsumoto, 2003, Muscle & nerve.

[A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].

M. Akaike, S. Kashiwagi, H. Kawai, 1995, Rinsho shinkeigaku = Clinical neurology.

Delayed motor and sensory neuropathy in a patient with brainstem encephalitis

I. Endo, T. Mitsui, Toshio Matsumoto, 2005, Journal of the Neurological Sciences.