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Featured researches published by Tadashi Matsubasa.


Journal of The American College of Nutrition | 1998

Zinc Status Relates to Hematological Deficits in Middle-Aged Women

Soroku Nishiyama; Kozo Irisa; Tadashi Matsubasa; Akimasa Higashi; Ichiro Matsuda

OBJECTIVE The objective of our study was to investigate zinc (Zn) status and the effects of Zn supplementation in relation to iron deficiency anemia in middle-aged women. It is important to define the role of Zn in hematologic abnormalities and to determine the frequency of Zn deficiency. METHODS Fifty-two Japanese women, selected from a health examination survey on 6200 women, had hemoglobin concentrations below 12.0 g/dl, total iron binding capacity (TIBC) below 390 micrograms/dl and fairly normocytemia. These 52 were divided into three groups and we then compared the hematological status before and after iron (group A) or Zn (group B) or iron plus Zn (group C) supplementation. RESULTS After treatment, concentrations of hemoglobin (Hb) increased slightly in groups A and B, but not statistically significant. In group C, Hb levels were significantly increased from 10.8 +/- 1.1 to 12.8 +/- 1.1 g/dl. Furthermore, numbers of RBC and reticulocytes, and concentrations of albumin were also increased significantly. Increased values over 1.0 g/dl of hemoglobin levels were noted in four women (26.6%) in group A, three women (14.2%) in group B and 13 women (81.2%) in group C. CONCLUSION Zn status to some extent can account for hematological abnormalities in middle-aged women. At least 5.0% of middle-aged Japanese women may have Zn deficiency. Normocytic anemia with low TIBC levels may serve as a good indicator of a marginal Zn deficiency.


Brain & Development | 1999

Helicobacter pylori seropositivity in patients with severe neurologic impairment.

Akihiko Kimura; Tadashi Matsubasa; Hirotoshi Kinoshita; Norikazu Kuriya; Yasuhiro Yamashita; Takuji Fujisawa; Hirotsugu Terakura; Makoto Shinohara

The objective of this study was to assess the prevalence of Helicobacter pylori seropositivity in institutionalized patients with severe neurologic impairment. Anti-H. pylori immunoglobulin G antibody in serum was measured in 196 institutionalized Japanese patients using enzyme linked immunosorbent assay, taking an antibody level >50 units/ml as evidence of H. pylori seropositivity. Patient age pattern and duration of institutionalization were examined for the relationships with H. pylori seropositivity. We also examined for seroconversion indicating new H. pylori infection in initially negative patients 1 year later. Positivity for H pylori infection among institutionalized patients was also compared with positivity among patients living at home. H. pylori seropositivity was present in 81.1% of subjects. Prevalence of H. pylori seropositivity increased with both age and duration of institutionalization. The serum level of anti-H. pylori immunoglobulin G antibody in patients over 20 years old was consistently high, approximately twice that of subjects less than 10 years of age. Of 38 patients initially negative for H. pylori infection, 18 (47.4%) had become positive at 1 year. H. pylori seropositivity was significantly more prevalent among institutionalized patients than among patients living at home (P < 0.0001). This study confirms that high H. pylori seropositivity rates are found among institutionalized patients with severe neurologic impairment. Our observations suggest person to person transmission, with fecal to oral, salivary secretion and respiratory droplet routes possibly being important pathways.


Pediatrics International | 2015

Time study of staff members in an institution for severe motor and intellectual disabilities

Tadashi Matsubasa; Akihiko Kimura; Makoto Shinohara; Fumio Endo

In Japan, improvement in the care for institutionalized patients with severe motor and intellectual disabilities (SMID) has resulted in improved prognosis compared with previous decades, leading to difficulty in entering institutions because of the limited capacity. In recent years, new SMID patients discharged mostly from neonatal intensive care units receive care in their parents’ homes rather than in institutions. In order to effect this change, an assessment of patient care in both an institutional and home environment is of utmost importance.


Pediatric Neurology | 1986

Carnitine prevents reye-like syndrome in atypical carnitine deficiency

Tadashi Matsubasa; Yoshinobu Ohtani; Teruhisa Miike; Akito Kitano; Fumio Endo; Ichiro Matsuda

A patient with repeated episodes of a Reye-like syndrome was studied. Serum and muscle carnitine levels were normal, but there was an apparent accumulation of muscle lipid and glycogen. Ragged-red fibers were present in the muscle. Prolonged fasting (20 hours) induced hypoglycemia, lactic acidosis, an increase in free fatty acids, and hyperammonemia. There was an accompanying sizeable reduction in the serum free carnitine level. Fasting with L-carnitine administration resulted in milder changes in these laboratory measures. Administration of L-carnitine, (100 mg/kg/day) led to clinical improvement as evidenced by fewer attacks and a normal Gowers sign.


Archive | 1991

Evolution of a Urea Cycle Enzyme to δ-Crystallin

Masataka Mori; Tadashi Matsubasa; Yoshihiro Amaya; Masaki Takiguchi

The urea cycle is closely related to the arginine biosynthetic pathway. It was thus expected that urea cycle enzymes evolved from arginine metabolic enzymes. cDNA clones for the mammalian urea cycle enzymes, ornithine trans- carbamylase, argininosuccinate lyase, and arginase, were isolated and sequenced, and the above view was confirmed. The amino acid sequences of the urea cycle enzymes are around 40% identical to those of the corresponding enzymes of the arginine metabolic pathways in microorganisms.


Free Radical Research | 2002

Oxidative stress in very low birth weight infants as measured by urinary 8-OHdG

Tadashi Matsubasa; Takako Uchino; Shinnyo Karashima; Masako Tanimura; Fumio Endo


BioEssays | 1989

Evolutionary aspects of urea cycle enzyme genes

Masaki Takiguchi; Tadashi Matsubasa; Yoshihiro Amaya; Masataka Mori


Journal of Biochemistry | 1988

Amino acid sequence of rat argininosuccinate lyase deduced from cDNA.

Yoshihiro Amaya; Tadashi Matsubasa; Masaki Takiguchi; Keiko Kobayashi; Takeyori Saheki; Susumu Kawamoto; Masataka Mori


Journal of Biochemistry | 1994

Rat Argininosuccinate Lyase Promoter: The Dyad-Symmetric CCAAT Box Sequence CCAATTGG in the Promoter Is Recognized by NF-Y

Tadashi Matsubasa; Masaki Takiguchi; Ichiro Matsuda; Masataka Mori


Pediatrics International | 2017

Medically dependent severe motor and intellectual disabilities: Time study of medical care

Tadashi Matsubasa; Hiroshi Mitsubuchi; Akihiko Kimura; Makoto Shinohara; Fumio Endo

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