Regulation of exercise-stimulated glucose uptake in skeletal muscle

por Koh, Ho-Jin
Publicado 2016

An update on the genetic causes of central precocious puberty

por Shin, Young-Lim
Publicado 2016

Predictive factors for early response to methimazole in children and adolescents with Graves disease: a single-institute study between 1993 and 2013

por Hwang, Sun Mi, Kim, Min Sun, Lee, Dae-Yeol
Publicado 2016

Ultrasound measurement of pediatric visceral fat thickness: correlations with metabolic and liver profiles

por Jung, Jae Hwa, Jung, Mo Kyung, Kim, Ki Eun, Kwon, Ah Reum, Chae, Hyun Wook, Yoon, Choon Sik, Kim, Ho Seong, Kim, Duk-Hee
Publicado 2016

The changes of subtypes in pediatric diabetes and their clinical and laboratory characteristics over the last 20 years

por Kwon, Eun Byul, Lee, Hae Sang, Shim, Young Seok, Jeong, Hwal Rim, Hwang, Jin Soon
Publicado 2016

Insulin and glucagon levels of umbilical cord blood in appropriate for gestational age - preterm infants with or without postnatal hypoglycemia

por Park, Jae Hyun, Bae, Jin Gon, Kim, Shin, Kim, Chun Soo, Lee, Sang Lak, Kim, Heung Sik
Publicado 2016

Dilated cardiomyopathy with Graves disease in a young child

por Choi, Yu Jung, Jang, Jun Ho, Park, So Hyun, Oh, Jin-Hee, Koh, Dae Kyun
Publicado 2016

Multiple daily injection of insulin regimen for a 10-month-old infant with type 1 diabetes mellitus and diabetic ketoacidosis

por Park, Ji Hyun, Shin, So Young, Shim, Ye Jee, Choi, Jin Hyeok, Kim, Heung Sik
Publicado 2016

A successful treatment of hypercalcemia with zoledronic acid in a 15-year-old boy with acute lymphoblastic leukemia

por Park, Hye-Jin, Choi, Eun-Jin, Kim, Jin-Kyung
Publicado 2016

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...

por Goto, Masahiro, Shibata, Nao, Hasegawa, Yukihiro
Publicado 2016

Potential utility of cinacalcet as a treatment for CDC73-related primary hyperparathyroidism: a case report

por Sato, Takeshi, Muroya, Koji, Hanakawa, Junko, Yamashita, Sumimasa, Nozawa, Kumiko, Masudo, Katsuhiko, Yamakawa, Tadashi, Asakura, Yumi, Hasegawa, Tomonobu, Adachi, Masanori
Publicado 2016

Chromosome 6q24 methylation defects are uncommon in childhood-onset non-autoimmune diabetes mellitus patients born appropriate- or large-for-gestational age

por Okuno, Misako, Yorifuji, Tohru, Kagami, Masayo, Ayabe, Tadayuki, Urakami, Tatsuhiko, Kawamura, Tomoyuki, Kikuchi, Nobuyuki, Yokota, Ichiro, Kikuchi, Toru, Amemiya, Shin, Suzuki, Junichi, Ogata, Tsutomu, Sugihara, Shigetaka, Fukami, Maki
Publicado 2016

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

por Nagahara, Keiko, Harada, Yuki, Futami, Tohru, Takagi, Masaki, Nishimura, Gen, Hasegawa, Yukihiro
Publicado 2016

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

por Higuchi, Shinji, Takagi, Masaki, Shimomura, Satoshi, Nishimura, Gen, Hasegawa, Yukihiro
Publicado 2016

A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1

por Tsunogai, Toshiki, Miyata, Ichiro, Kotake, Saori, Matsuura, Ryuki, Takagi, Ken, Nanba, Hiroyuki, Takahata, Noriko, Tajima, Toshihiro, Wada, Yasuyuki
Publicado 2016

A novel frameshift mutation in the TRPS1 gene caused Tricho-rhino-phalangeal syndrome type I and III in a Japanese family

por Itoh, Masatsune, Kittaka, Yuko, Niida, Yo, Saikawa, Yutaka
Publicado 2016

Longitudinal observation of serum anti-Müllerian hormone in three girls after cancer treatment

por Miyoshi, Yoko, Yasuda, Kie, Tachibana, Makiko, Yoshida, Hisao, Miyashita, Emiko, Miyamura, Takako, Hashii, Yoshiko, Hashimoto, Kae, Kimura, Tadashi, Ozono, Keiichi
Publicado 2016

A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation

por Mitani, Marie, Furuichi, Munehiro, Narumi, Satoshi, Hasegawa, Tomonobu, Chiga, Motoko, Uchida, Shinichi, Sato, Seiji
Publicado 2016

A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1

por Nishizaki, Yoshimi, Hiura, Makoto, Sato, Hidetoshi, Ogawa, Yohei, Saitoh, Akihiko, Nagasaki, Keisuke
Publicado 2016

A case of transient neonatal diabetes due to a novel mutation in ABCC8

por Takagi, Masaki, Takeda, Ryojun, Yagi, Hiroko, Ariyasu, Daisuke, Fukuzawa, Ryuji, Hasegawa, Tomonobu
Publicado 2016