Eiichi Kinoshita

Compound Heterozygous Deletion of the<i>PROP</i>-1 Gene in Children with Combined Pituitary Hormone Deficiency

Q. Fofanova, Noboru Takamura, Eiichi Kinoshita et al. · The Journal of Clinical Endocrinology & Metabolism · 1998 · 127 citations

Russian Children, Systems Biology, Developmental Biology +13

Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome

Rie Yoshida, Tomonobu Hasegawa, Yukihiro Hasegawa et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 111 citations · Full text

Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype

Sumito Dateki, Kitaro Kosaka, Kosei Hasegawa et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 107 citations

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome

Takehisa Yamamoto, Yasuo Imanishi, Eiichi Kinoshita et al. · Journal of Bone and Mineral Metabolism · 2005 · 66 citations

Metabolic Syndrome, Metabolic Disorder, Vitamin D Metabolism +10

MR Imaging of the Pituitary Gland in Children and Young Adults with Congenital Combined Pituitary Hormone Deficiency Associated with <i>PROP1</i> Mutations

Noboru Takamura, Eiichi Kinoshita, Alexander Vorontsov et al. · American Journal of Roentgenology · 2000 · 63 citations