JOURNAL OF THE KYORIN MEDICAL SOCIETY
Online ISSN : 1349-886X
Print ISSN : 0368-5829
ISSN-L : 0368-5829
Volume 29, Issue 1
Displaying 1-50 of 139 articles from this issue
  • Article type: Cover
    1998 Volume 29 Issue 1 Pages Cover1-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (89K)
  • Article type: Cover
    1998 Volume 29 Issue 1 Pages Cover2-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (89K)
  • [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 1-2
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (260K)
  • Toshiaki MARUYAMA
    Article type: Article
    1998 Volume 29 Issue 1 Pages 3-15
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    After a bone defect was made in the coccygeal vertebra in rat models of experimental osteoporosis, changes in X-ray and histopathological features, bone metabolic markers, and bone mineral density were investigated over time. These parameters were compared among 3 groups, the bone defect group (46 rats), the ovariectomized (OVX) group (30 rats), and the Sham operated group (30 rats), after ovariectomy was performed on 106 female Wistar rats at the age of 12 weeks. Both X-ray and histopathological features demonstrated that the bone defect was repaired over time. In the bone defect group, there were time lags between the changes in bone metabolic markers and those in BMD. Bone metabolism was high turneover rate when a defect was made in the vertebral bodywith osteoporosis, leading to the increase in BMD. These results suggested a possibility that an increase or decrease in BMD, predicted by means of measurement of bone metabolic markers, can serve as an indicator for differential diagnoses of clinical cases. In the particular case of fresh spinal compression fracture with osteoporosis, it should be important to consider the high turnover of bone metabolism and reactive bone formation in local sites.
    Download PDF (2858K)
  • Hiroshi IRIE
    Article type: Article
    1998 Volume 29 Issue 1 Pages 17-33
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Somatosensory evoked potentials (SEPs) following posterior tibial nerve stimulation were studied in 35 normal subjects by linkedears reference derivation and source derivation techniques. The effects of height on the latencies and amplitudes of each SEP component, correlations among each component latencies, and among those amplitudes, scalp topographies and differences between stimulus sides were evaluated. The latencies of N32, P40 and N50 were highly correlated to height, but that of N75 was not correlated to height. The latencies except P60 and N75 were correlated each other. Amplitude values of N50, P60 and N75 were correlated to that of P40, but not to height. N75 amplitude was also correlated to P60 amplitude. The scalp topographies of P40 and N50 showed the pattern of tangential dipole type and those of P60 and N75 were the pattern of radial dipole type. These results suggest that the generators and generating mechanisms are different between P40-N50 and P60-N75. With regard to P40, the former half may be generated from area 3b and the latter half from area 1. Therefore, P40 is a compound potential generated from areas 3b and 1. Source derivation is more useful in these experiments than linked-ears reference derivation.
    Download PDF (1758K)
  • Azusa KIKUKAWA
    Article type: Article
    1998 Volume 29 Issue 1 Pages 35-43
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Research investigating the relationship between physical training and trace mineral concentrations has focused primarily on athletes. Exercise alters mineral content; flight is a form of exercise; therefore, flight may elicit changes in mineral content. This study examined the effects of stressful flight aptitude tests on the trace minerals zinc and copper in urine. During flight aptitude tests, urine samples were obtained from 100 men. The zinc concentration decreased following flight. Furthermore, because +Gz acceleration is one of many stressors for an aviator in flight, the effects of +Gz acceleration on the trace minerals zinc, copper, and chromium in human serum and urine were also examined. Blood and urine samples were obtained from 7 men and 3 women, before and after +Gz acceleration. The serum zinc and copper concentrations decreased after +Gz acceleration. The urinary zinc and copper concentrations were not altered by +Gz acceleration. These findings suggest that the circulating levels of zinc and copper presumably change as they are transported to tissues requiring greater amounts due to the increased physiological work associated with flight stress, including +Gz acceleration.
    Download PDF (783K)
  • Mamoru TASHIRO
    Article type: Article
    1998 Volume 29 Issue 1 Pages 45-52
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    The advantage of perfluorocarbon (PFC) emulsion priming for veno-arterial extracorporeal membrane oxygenation (ECMO) was evaluated by comparison with hydroxyethyl starch (HES) solution in rabbits (2.8-3.9 kg). ECMO initiation was accompanied by a profound decrease in hematocrit (from approx. 40% to 15%) in both groups. The arterial and the right atrial oxygen contents in the PFC group (n=4 ; 38.5 and 11.5mL/dL) were greater than in the HES group (n=5 ; 7.0 and 5.1mL/dL). However, plasma lactate progressively increased during 120 min ECMO procedure in both groups (from 1.8 to 14.5mmol/L ; the HES group, from 2.3 to 12.2mmol/L; the PFC group). We conclude that perfluorocarbon priming for ECMO, although it provides high oxygen delivery and extraction, do not prevent the anaerobic metabolism in rabbits.
    Download PDF (694K)
  • Masahiro MARUYAMA
    Article type: Article
    1998 Volume 29 Issue 1 Pages 53-64
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Glucose transport activities of isolated rat adipocytes were measured after 4 and 1 hour incubation with KRB buffer containing 5.5, 11, 22 or 44 mM glucose with/without insulin. When rat adipocytes were pre-exposed to 11 mM glucose for 4h, glucose transport activity was increased by 80 % compared to that of adipocytes pre-exposed to 5.5 mM glucose (control). In contrast, pre-exposure to 44 mM glucose rather inhibited the glucose transport activity to 74 %, and such an inhibitory effect was disappeared by placing adipocytes in 5.5mM glucose for 1 h. In an attempt to elucidate the effect of osmolarity on glucose transport, rat adipocytes were incubated with 5.5 mM glucose plus 38.5 mM glycerol. The transport activity was increased by about 40 % of that of control, suggesting that there is no relationship between osmolarity and decreased glucose transport activity caused by 44 mM glucose pre-exposure. Furthermore, the glucose transporter 4 (GLUT4) protein levels investigated by an immunoblotting analysis demons trated that this pre-exposure to glucose did not decrease GLUT4 protein levels in either plasma membranes or total cell lysates. The results indicated that extreme high concentrations of glucose decreased the glucose transport activity of rat adipocytes, probably via the decreased intrinsic activity of GLUT4 protein.
    Download PDF (1124K)
  • Nobuyuki MIYAKE
    Article type: Article
    1998 Volume 29 Issue 1 Pages 65-74
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    The purpose of this study was to elucidate the role of renal heme oxygenase (HO)-1 and glutathione (GSH) in acquired resistance in glycerol-induced acute renal failure (ARF) of rats. Prior administration of glycerol conferred resistance to glycerol-induced ARF morphologically as well as functionally (acquired resistance). In glycerol-treated rats, HO-1 mRNA expression determined by reverse transcription-polymerase chain reaction was induced, whereas renal GSH content was significantly decreased. Pretreatment with tinprotoporphyrin, a specific and competitive inhibitor of HO-1 blocked the acquired resistance in glycerol-induced ARF and the increase in level of HO-1 mRNA expression, and restored the level of renal GSH content up to the level similar to that of control. These results suggest that HO-1 is at least in part responsible for the acquired resistance in glycerol-ARF in rats. In addition, the results also raise the intriguing possibility that GSH exhibits direct as well as indirect antioxidative effects through the induction of HO-1.
    Download PDF (1589K)
  • Tsutomu OHASHI
    Article type: Article
    1998 Volume 29 Issue 1 Pages 75-82
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    The impedance cuff method is a newly developed technique for evaluating the peripheral circulation, giving the peripheral blood flow (BF) and volume elastic modulus (Ev) which indicates the elastance of peripheral arteries. Twenty-three patients undergoing gynecologic surgery were anesthetized with isoflurane (Group I, n=12) or sevoflurane (Group S, n=11), and the impedance cuff method was applied to the left index finger. Arterial blood pressure and pulse rate were then monitored. The volatile anesthetics at 1.3 minimum alveolar concentration (MAC) or 0.4 MAC were serially administered with 66 % nitrous oxide and the remainder oxygen for 30min, respectively, and the data were collected every 5 min. There was no significant intra- or inter-group difference in the arterial blood pressure. Pulse rate was significantly higher (p<0.05) in Group I than in Group S. BF was significantly lower in Group I than in Group S at 1.3 MAC. The value of Ev decreased after induction of anesthesia in both groups, and remained low in Group I, whereas it increased in Group S at 0.4 MAC. Ev in Group I was significantly lower than that in Group S at 0.4 MAC (p<0.05). These data suggest that Ev measured by the impedance cuff method is a sensitive parameter for monitoring the peripheral circulation.
    Download PDF (672K)
  • Yuko KATSUMATA
    Article type: Article
    1998 Volume 29 Issue 1 Pages 83-93
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    The subzonal insemination (SUZI) and the intracytoplasmic sperm injection (ICSI) were performed for the treatment of severe male infertility. The rates of fertilization per oocyte and pregnancy per cycle in severe male infertility were 3 % and 0 % with conventional in vitro fertilization (IVF) (10 cycles) and 18 % and 11 % with SUZI (27 cycles). The rates of fertilization and pregnancy in severe male infertility were improved by SUZI, but they were still lower than those with conventional IVF in the tubal infertility with normal male partner (fertilization rate : 66%, pregnancy rate : 27%, 133 cycles). The rates of fertilization and pregnancy in severe male infertility were 17 % and 0 % with conventional ICSI(15 cycles) and 63 % and 34 % with devised ICSI (74 cycles). In 4 cases with azoospermia, devised ICSI with testicular sperm extraction (TESE) were attempted. Two cases resulted in ongoing pregnancies. Next, human sperm from severe male infertility patients was injected into the hamster oocytes to analyze factors contributing to improvement in clinical outcome in this study. The rate of fertilization with ICSI using hamster oocytes were lower in the group using high concentration of sperm in sperm droplet than in the group using low concentration of sperm. The deterioration in the rate of fertilization was improved by changing medium in the sperm suspension. The levels of endotoxin in sperm suspension were significantly higher with high concentration of sperm than with low concentration. This result suggests endotoxin in sperm suspension decreases the rate of fertilization in ICSI. This study showes the adequately devised ICSI is highly effective in the treatment for severe male infertility.
    Download PDF (1107K)
  • Yasushi NAGASHIMA
    Article type: Article
    1998 Volume 29 Issue 1 Pages 95-105
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    In order to clarify a pathophysiological role of protein kinase (PKase) existed in a hypotonic extract of nuclei, effect of anticarcinogenic agent, cisplatin, on the enzyme activity was investigated in transplanted tumor tissue in mice. The expression level of the oncogene or suppressor oncogene was simultaneously determined. A hypotonic extracts of nuclei was prepared from tumor tissue of BALB/c mice transplanted with Meth A cell. The extract (ENP, extractable nuclear protein) was further separated into fractions by DEAE-Sepharose column chromatography with a stepweise NaCl concentration gradient elution. The protein kinase activity in those fractions was measured with casein and [^<32>P] ATP as the substrates. K-ras and p53 gene expression were determined by the use of RT-PCR method followed by QPCR method. Cisplatin decreased high PKase activity in 0.15 M NaCl-containing fraction obtained from tumor tissue, but increased the activity in 0.3 M NaCl fraction. Cisplatin enhanced the level of both K-ras and p53 gene expression. These results suggest that extractable nuclear protein kinase especially in 0.3 M fraction seems to be working on the suppression of cell proliferation and the increase of the enzyme activity would be associated with the increase of expression level of both the oncogene and suppressor oncogene in tumor cell.
    Download PDF (1131K)
  • Masanori TOBE
    Article type: Article
    1998 Volume 29 Issue 1 Pages 107-118
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    To elucidate the function and the role of nuclear protein kinases, which was found in a hypotonic extracts of nuclei, the effect of hyperthermic treatment on the enzymatic activity in tumor tissue was investigated together with the changes in the concentration of stress protein and apoptosis associated protein in the cytosol fraction obtained from tumor tissue (Meth A fibrosarcoma) in BALB / c mice. Hyperthermic treatment inhibited the tumor development and decreased the DNA synthesis in the tumor tissue. The treatment decreased the extractable nuclear PKase activity in 0.15 M NaCl-containing fraction but increased it in 0.3 M NaCl containing fraction, which were prepared from the extracts by a DEAE-Sepharose column chromatography. The treatment also decreased the cytosomal HSP60 and Fas protein contents in tumor tissue. These results suggest the deviation of the signal transduction system in tumor tissue from the normal one, and involvement of the extractable nuclear PKase in cell proliferation and / or apoptosis induction mechanisms.
    Download PDF (1196K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 119-120
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (267K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 120-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (206K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 120-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (206K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 121-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (192K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 121-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (192K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 121-122
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (336K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 122-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (197K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 122-123
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (332K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 123-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (191K)
  • [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 123-124
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (300K)
  • [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 124-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (162K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 124-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (162K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 125-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (192K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 125-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (192K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 125-126
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (338K)
  • [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 126-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (202K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 126-127
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (340K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 127-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (197K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 127-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (197K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 128-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (196K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 128-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (196K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 128-129
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (331K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 129-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (192K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 129-130
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (337K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 130-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (204K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 130-131
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (347K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 131-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (206K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 131-132
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (327K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 132-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (180K)
  • [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 132-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (180K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 133-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (156K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 133-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (156K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 134-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (182K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese]
    Article type: Article
    1998 Volume 29 Issue 1 Pages 134-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (182K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 135-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (190K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 135-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (190K)
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    Article type: Article
    1998 Volume 29 Issue 1 Pages 136-
    Published: March 31, 1998
    Released on J-STAGE: February 13, 2017
    JOURNAL FREE ACCESS
    Download PDF (183K)
feedback
Top