Kenichi Iseki

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  • Kenichi Iseki
  • [Hokkaido igaku zasshi] The Hokkaido journal of…
  • 1987
The development of faecal bacterial flora was studied using quantitative anaerobic and aerobic culture methods to determine the differences between various types of feeding. Enterobacteria first colonized predominantly in neonatal intestine, and their viable counts on the first day of life were between 10(8)-10(10) per gram faeces. In the breast-fed group,(More)
Hand-preference data of 2316 Japanese were analyzed by age groups, sex, and familial sinistrality. Right-hand preference increased across age groups at least up to 30 years for men, while women showed relatively stable and stronger preference for right-hand use. Unlike some Western studies, no linear trends across age groups were found for both sexes.(More)
Protein-losing enteropathy (PLE) is a rare and life-threatening complication that occurs after the Fontan procedure. We herein report the case of an 11-year-old Japanese boy who developed PLE six times after undergoing the Fontan procedure. High-dose spironolactone therapy has been effective for 2 years. His high level of serum aldosterone decreased to a(More)
OBJECTIVE To evaluate the parameters associated with significant gastrointestinal (GI) involvement in Henoch-Schönlein Purpura (HSP), and construct a scoring system for the identification of patients at high risk of gross blood in stools. STUDY DESIGN Data for HSP patients hospitalized at each of seven institutes were retrospectively analyzed. Patients(More)
BACKGROUND Disseminated neonatal herpes simplex virus (HSV) infection causes a typical systemic inflammatory response syndrome and has a high mortality rate. However, the validity of anti-inflammatory intervention against this condition remains unknown. OBJECTIVES We sought to demonstrate the sequential changes in the pathophysiology of disseminated(More)
MYH9 disorder is a rare autosomal dominant disease characterized by congenital thrombocytopenia with giant platelets and leukocyte inclusion bodies and is often associated with Alport-like symptoms, such as glomerulonephritis, sensorineural hearing loss, and cataracts. We report a Japanese pedigree wherein the MYH9 p.R1165C mutation was present in over 4(More)
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