Katsuhiko Tachibana


Ontology type: schema:Person     


Person Info

NAME

Katsuhiko

SURNAME

Tachibana

Publications in SciGraph latest 50 shown

  • 2004-04 Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation in EUROPEAN JOURNAL OF PEDIATRICS
  • 2000-11 Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development in HUMAN GENETICS
  • 2000-10 Three Novel PHEX Gene Mutations in Japanese Patients with X-Linked Hypophosphatemic Rickets in PEDIATRIC RESEARCH
  • 2000-03 Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features in HUMAN GENETICS
  • 1998-12 Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion in EUROPEAN JOURNAL OF PEDIATRICS
  • 1997-07 Osteopathia striata, short stature, and characteristic facies: a previously unknown skeletal dysplasia in EUROPEAN JOURNAL OF PEDIATRICS
  • 1996-12 Monthly Urinary Gonadotropin and Ovarian Hormone Excretory Patterns in Normal Girls and Female Patients with Idiopathic Precocious Puberty in PEDIATRIC RESEARCH
  • 1996-08 Mental retardation — megaepiphyses —ulnar pseudoepiphyses — hypoplastic fibulae — brachymesophalangia: A new syndrome in PEDIATRIC RADIOLOGY
  • 1993-05 MONTHLY URINARY GONADOTROPIN AND OVARIAN HORMONE SECRETORY PATTERNS IN NORMAL CHILDREN AND PATIENTS WITH IDIOPATHIC PRECOCIOUS PUBERTY in PEDIATRIC RESEARCH
  • 1993-05 LATE ADRENARCHE IN A PATIENT WITH PSEUDORYPOPARATHYROIDISM (PHP): APPLICATION OF OF A NEWLY DEVELOPED ELISA FOR DUEAS in PEDIATRIC RESEARCH
  • 1990-10 Quantitation of Urinary Gonadotropins in Normal Children in PEDIATRIC RESEARCH
  • 1990-10 Monthly Urinary LH and FSH Secretory Patterns in Normal Children and Patients with Sexual Disorders in PEDIATRIC RESEARCH
  • 1985-12 Prolonged Activation of Hypothalamo-Pituitary-Ovarian Axis during Early Infancy in Female Patients with Salt-Losing 21-Hydroxylase Deficiency in PEDIATRIC RESEARCH
  • 1980-05 Cerebro-costo-mandibular syndrome in HUMAN GENETICS
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