Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Hidetoshi FUKUNAGA"'
Publikováno v:
Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 49:491-495
We report a patient with optic neuropathy and longitudinally extensive myelitis associated with anti-aquaporin 4 (AQP4) antibody and other autoantibodies. An 89-year-old woman presented with progressive numbness and weakness of the extremities which
Autor:
Yoshito Sonoda, Fujio Umehara, Joeji Wakimoto, Yuichi Uchida, Kyoko Maruta, Hidetoshi Fukunaga
Publikováno v:
Rinsho Shinkeigaku. 50:232-240
A 64-year-old woman was referred to our hospital because of disturbance of consciousness. She had undergone distal gastrectomy for gastric carcinoma 17 years previously. General physical examination was unremarkable, neurologic examination disclosed
Autor:
Mitsuhiro Osame, Ikuro Maruyama, Hidetoshi Fukunaga, Takefumi Kasai, Kazuhiro Abeyama, Teruto Hashiguchi
Publikováno v:
Journal of Biomedical Science. 11:534-537
Plasma nitric oxide (NO) levels in Duchenne muscular dystrophy (DMD) patients were significantly lower than those observed in both healthy controls and in patients with other neuromuscular disorders. The correlation between NO level and ejection frac
Publikováno v:
Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 41:339-343
A 72-year-old woman with von Recklinghausen's disease was referred to our hospital because of pain and muscle weakness in her thighs. She had elevated serum values of creatine kinase, aspartate aminotransferase, alanine aminotransferase, lactate dehy
Autor:
Masanori Nakagawa, Makoto Kunishige, Hiroyuki Iwaki, Mitsuhiro Osame, Itsuro Higuchi, Hisaomi Kawai, Takenori Endo, Hidetoshi Fukunaga, Kimiyoshi Arimura
Publikováno v:
Journal of the Neurological Sciences. 153:100-105
A new homozygous alpha-sarcoglycan (adhalin) gene mutation was found in a Japanese patient with severe childhood autosomal recessive muscular dystrophy (SCARMD). Muscle biopsy specimens from the patient showed marked reduction but not complete defici
Publikováno v:
European Neurology. 38:64-69
We analyzed patients with Parkinson's disease from various aspects such as clinical findings, the degree of independence in daily life, care environment, quality of life (QOL) and treatment at home. The subjects were 104 in- and outpatients (47 males
Autor:
Hidetoshi Fukunaga
Publikováno v:
Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 42:186-188
Autor:
Masanori Nakagawa, Masaru Inose, Naohito Niiyama, Hidetoshi Fukunaga, Kimiyoshi Arimura, Takahashi Goto, Fukuo Motokura, Mitsuhiro Osame, Itsuro Higuchi, Ryuichi Ohkubo, Khotaro Izumi
Publikováno v:
Journal of the Neurological Sciences. 143:79-83
We have reported the reduction of the B1 subunit of laminin and that of heparan sulfate proteoglycan (HSPG) in two Japanese patients with adhalin deficiency. We here investigated immunohistochemically the expression of cell adhesion molecules, includ
Publikováno v:
Muscle & Nerve. 16:554-558
We, retrospectively, examined the clinical course, decline in pulmonary function, and requirements for ventilatory assistance in 54 patients with Duchenne-type muscular dystrophy (DMD) who were followed in the muscle disease ward of the National Hosp
Publikováno v:
Internal Medicine. 31:973-977
Recent epidemiologic studies have shown that human T-lymphotropic virus type I (HTLV-I) is associated with polymyositis. To clarify the histological features of HTLV-I positive polymyositis, we studied muscle tissue from two groups of patients with p