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Results of search for 'au:"Kunishige, M"', page 1 of 2
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Authors
Akaike, M
Aki, K
Endo, I
Endo, T
Halangoda, A
Hill, K A
Kashiwagi, S
Kawai, H
Kawajiri, M
Komatsu, M
Kunishige, M
Matsumoto, T
Mine, H
Mitsui, T
Moore, S R
Nishida, Y
Oshima, Y
Saito, S
Shono, M
Yokoi, K
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Adolescent
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Aged
Animals
Child
Cytoskeletal Proteins
DNA, Mitochondrial
Dermatomyositis
Female
Humans
Magnetic Resonance Imaging
Male
Mice
Middle Aged
Muscle, Skeletal
analysis
complications
genetics
metabolism
pathology
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Your search returned 25 results.
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1.
Dermatomyositis associated with impairment in both muscle aerobic and anaerobic function.
[electronic resource]
by
Kunishige, M
Mitsui, T
Endo, I
Matsumoto, T
Producer:
20050222
In:
Clinical neuropathology
vol. 24
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2.
[A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].
[electronic resource]
by
Akaike, M
Kawai, H
Kashiwagi, S
Kunishige, M
Saito, S
Producer:
19950718
In:
Rinsho shinkeigaku = Clinical neurology
vol. 35
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3.
Preferential subsarcolemmal localization of dystrophin and beta-dystroglycan mRNA in human skeletal muscles.
[electronic resource]
by
Mitsui, T
Kawai, H
Shono, M
Kawajiri, M
Kunishige, M
Saito, S
Producer:
19970131
In:
Journal of neuropathology and experimental neurology
vol. 56
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4.
Localization and amount of myoglobin and myoglobin mRNA in ragged-red fiber of patients with mitochondrial encephalomyopathy.
[electronic resource]
by
Kunishige, M
Mitsui, T
Akaike, M
Shono, M
Kawai, H
Saito, S
Producer:
19960228
In:
Muscle & nerve
vol. 19
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5.
Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice.
[electronic resource]
by
Mitsui, T
Kawai, H
Kawajiri, M
Kunishige, M
Aki, K
Saito, S
Producer:
19960910
In:
Biochemical and biophysical research communications
vol. 224
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6.
Systemic muscular inflammation in a patient with recurrent orbital myositis.
[electronic resource]
by
Omori, H
Mitsui, T
Kunishige, M
Endo, I
Takahashi, K
Matsumoto, T
Producer:
20051026
In:
Clinical neuropathology
vol. 24
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7.
Thyrotoxicosis masked by diabetic ketoacidosis: a fatal complication.
[electronic resource]
by
Kunishige, M
Sekimoto, E
Komatsu, M
Bando, Y
Uehara, H
Izumi, K
Producer:
20010531
In:
Diabetes care
vol. 24
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8.
Dermatomyositis associated with Sjögren's syndrome: VEGF involvement in vasculitis.
[electronic resource]
by
Ohno, A
Mitsui, T
Endo, I
Kunishige, M
Sigekiyo, T
Matsumoto, T
Producer:
20040930
In:
Clinical neuropathology
vol. 23
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9.
Syndrome of inappropriate secretion of ADH (SIADH) due to small cell lung cancer with extremely high plasma vasopressin level.
[electronic resource]
by
Mizobuchi, M
Kunishige, M
Kubo, K
Komatsu, M
Bando, H
Saito, S
Producer:
19950131
In:
Internal medicine (Tokyo, Japan)
vol. 33
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10.
Functional association between nicotinic acetylcholine receptor and sarcomeric proteins via actin and desmin filaments.
[electronic resource]
by
Mitsui, T
Kawajiri, M
Kunishige, M
Endo, T
Akaike, M
Aki, K
Matsumoto, T
Producer:
20000815
In:
Journal of cellular biochemistry
vol. 77
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11.
Interferon alpha-2a therapy for disseminated intravascular coagulation in a patient with blue rubber bleb nevus syndrome. A case report.
[electronic resource]
by
Kunishige, M
Azuma, H
Masuda, K
Shigekiyo, T
Arii, Y
Kawai, H
Saito, S
Producer:
19970409
In:
Angiology
vol. 48
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12.
Lysosomal enzyme activities in skeletal muscle of patients with neuromuscular diseases.
[electronic resource]
by
Kawai, H
Yoneda, K
Naruo, T
Nishida, Y
Kashiwagi, S
Kunishige, M
Saito, S
Producer:
19950919
In:
Muscle & nerve
vol. 18
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13.
Cardiac dysfunction in patients with chronic progressive external ophthalmoplegia.
[electronic resource]
by
Akaike, M
Kawai, H
Yokoi, K
Kunishige, M
Mine, H
Nishida, Y
Saito, S
Producer:
19970523
In:
Clinical cardiology
vol. 20
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14.
Lethal encephalopathy in a patient with isolated nervous system vasculitis.
[electronic resource]
by
Sumitomo, Y
Kunishige, M
Satake, N
Shinno, K
Kawashima, M
Matsumoto, T
Mitsui, T
Producer:
20041222
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 75
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15.
Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases.
[electronic resource]
by
Kawai, H
Akaike, M
Yokoi, K
Nishida, Y
Kunishige, M
Mine, H
Saito, S
Producer:
19950720
In:
Muscle & nerve
vol. 18
Online resources:
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16.
Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies.
[electronic resource]
by
Mitsui, T
Kawai, H
Nagasawa, M
Kunishige, M
Akaike, M
Kimura, Y
Saito, S
Producer:
19961223
In:
Journal of the neurological sciences
vol. 139
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17.
Central motor conduction in patients with anti-ganglioside antibody associated neuropathy syndromes and hyperreflexia.
[electronic resource]
by
Oshima, Y
Mitsui, T
Yoshino, H
Endo, I
Kunishige, M
Asano, A
Matsumoto, T
Producer:
20030110
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 73
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18.
[Case of non-trauma forearm compartment syndrome with prominent hypermyoglobinemia].
[electronic resource]
by
Kawai, K
Matsuda, K
Kameyama, K
Oka, K
Naruse, A
Kano, M
Kunishige, M
Kawashiri, M
Producer:
19970212
In:
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine
vol. 85
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19.
Severe dermatomyositis with rhabdomyolysis and paralytic ileus: a case successfully treated with plasmapheresis and intravenous immunoglobulin.
[electronic resource]
by
Fukunaga, E
Kunishige, M
Mitsui, T
Endo, I
Oshima, Y
Ohnishi, Y
Kuroda, Y
Hara, S
Matsumoto, T
Producer:
20030210
In:
European journal of neurology
vol. 9
Online resources:
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20.
New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency.
[electronic resource]
by
Higuchi, I
Iwaki, H
Kawai, H
Endo, T
Kunishige, M
Fukunaga, H
Nakagawa, M
Arimura, K
Osame, M
Producer:
19980305
In:
Journal of the neurological sciences
vol. 153
Online resources:
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