Dose Adjustments of Hydrocortisone and L-thyroxine in Hypopituitarism Associated with Cholestasis

by Higuchi, Asako, Hasegawa, Yukihiro
Published 2006

Limitations of G-banding Karyotype Analysis with Peripheral Lymphocytes in Diagnosing Mixed Gonadal Dysgenesis

by Takahashi, Ikuko, Miyamoto, Junko, Hasegawa, Yukihiro
Published 2006

Efficacy of single serum cortisol reading obtained between 9 AM and 10 AM as an index of adrenal function in children treated with glucocorticoids or synthetic adrenocorticotropic...

by Goto, Masahiro, Shibata, Nao, Hasegawa, Yukihiro
Published 2016

Pregnanetriol in the Range of 1.2–2.1 mg/m2/day as an Index of Optimal Control in CYP21A2 Deficiency

by Izawa, Masako, Aso, Keiko, Higuchi, Asako, Ariyasu, Daisuke, Hasegawa, Yukihiro
Published 2007

Stress Doses of Glucocorticoids Cannot Prevent Progression of All Adrenal Crises

by Aso, Keiko, Izawa, Masako, Higuchi, Asako, Kotoh, Shinobu, Hasegawa, Yukihiro
Published 2009

The Range of 2.2–3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency

by Izawa, Masako, Aso, Keiko, Higuchi, Asako, Ariyasu, Daisuke, Hasegawa, Yukihiro
Published 2008

Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset

by Fukuma, Mami, Ariyasu, Daisuke, Hatano, Megumi, Yagi, Hiroko, Hasegawa, Yukihiro
Published 2016

A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1

by Higuchi, Shinji, Takagi, Masaki, Shimomura, Satoshi, Nishimura, Gen, Hasegawa, Yukihiro
Published 2016

Identification of X Monosomy Cells From a Gonad of Mixed Gonadal Dysgenesis With a 46,XY Karyotype: Case Report

by Nishina-Uchida, Noriko, Fukuzawa, Ryuji, Hasegawa, Yukihiro, Morison, Ian M.
Published 2015

Single serum cortisol values at 09:00 h can be indices of adrenocortical function in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone

by Goto, Masahiro, Miyagawa, Naoyuki, Kikunaga, Kaori, Miura, Masaru, Hasegawa, Yukihiro
Published 2015

High incidence of adrenal suppression in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone

by Goto, Masahiro, Miyagawa, Naoyuki, Kikunaga, Kaori, Miura, Masaru, Hasegawa, Yukihiro
Published 2015

A novel KAL1 mutation is associated with combined pituitary hormone deficiency

by Takagi, Masaki, Narumi, Satoshi, Hamada, Riku, Hasegawa, Yukihiro, Hasegawa, Tomonobu
Published 2014

Increased Secretion of Endogenous GH after Treatment with an Intranasal GH-releasing Peptide-2 Spray Does Not Promote Growth in Short Children with GH Deficiency

by Tanaka, Toshiaki, Hasegawa, Yukihiro, Yokoya, Susumu, Nishi, Yoshikazu
Published 2014

A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus

by Daitsu, Takashi, Igaki, Junko, Goto, Masahiro, Hasegawa, Yukihiro
Published 2014

Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood

by Suzuki, Eri, Yamada, Makoto, Ariyasu, Daisuke, Izawa, Masako, Miyamoto, Junko, Koto, Shinobu, Hasegawa, Yukihiro
Published 2009

Gonadal Function in 15 Patients Associated with WT1 Gene Mutations

by Maesaka, Akiko, Higuchi, Asako, Kotoh, Shinobu, Hasegawa, Yukihiro, Ikeda, Masahiro, Shishido, Seiichirou, Honda, Masataka
Published 2006

Mutational Analysis of Androgen Receptor (AR) Gene in 46,XY Patients with Ambiguous Genitalia and Normal Testosterone Secretion: Endocrinological Characteristics of Three Patients...

by Miyamoto, Junko, Asanuma, Hiroshi, Nakai, Hideo, Hasegawa, Tomonobu, Nawata, Hajime, Hasegawa, Yukihiro
Published 2006

A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3

by Nagahara, Keiko, Harada, Yuki, Futami, Tohru, Takagi, Masaki, Nishimura, Gen, Hasegawa, Yukihiro
Published 2016

A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide

by Takeda, Ryojun, Takagi, Masaki, Miyai, Kentaro, Shinohara, Hiroyuki, Yagi, Hiroko, Moritani, Maki, Yokota, Ichiro, Hasegawa, Yukihiro
Published 2015

A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2

by Takagi, Masaki, Yagi, Hiroko, Nakamura, Yoshie, Shinohara, Hiroyuki, Takeda, Ryojun, Shimada, Aya, Nishimura, Gen, Hasegawa, Yukihiro
Published 2015