Shigenori Yukizane

ASPLENIA AND POLYSPLENIA SYNDROME

Yasuyuki Shinohara, Setsuro Komiya, A. Nakashima et al. · Acta Pathologica Japonica · 1982 · 158 citations

Medicine, Anatomy, Pediatrics +15

No Enzyme Activity of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

Sachiko Kitanaka, Akiko Murayama, Toshiyuki Sakaki et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 75 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Congenital Hypothyroidism Caused by a Unique Thyroid Peroxidase Allele Containing Two Mutations, C1708T and C2737T

Kazumi Umeki, Ikuo Yamamoto, Shigenori Yukizane et al. · Journal of Pediatric Endocrinology and Metabolism · 2004 · 21 citations

Life Sciences, Genetics, Molecular Genetics +13

A point mutation in exon 3 (His 107→Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement

Hiroko Soda, Shigenori Yukizane, Ichiro Yoshida et al. · Human Genetics · 1996 · 20 citations

Life Sciences, Genetics, Molecular Genetics +9

Growth hormone deficiency of hypothalamic origin in septo-optic dysplasia

Shigenori Yukizane, Y Kimura, Yushiro Yamashita et al. · European Journal of Pediatrics · 1990 · 19 citations

Medicine, Endocrinology, Neuroscience +15