Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey

por Fujiwara, Makoto, Namba, Noriyuki, Ozono, Keiichi, Arisaka, Osamu, Yokoya, Susumu
Publicado 2013

Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia: New Understanding

por Ozono, Keiichi, Michigami, Toshimi, Namba, Noriyuki, Nakajima, Shigeo, Yamamoto, Takehisa
Publicado 2006

Successful Treatment of Cyst Infection in an Infant With Autosomal Dominant Polycystic Kidney Disease Using Trimethoprim/Sulfamethoxazole

por Yokoyama, Hiroki, Sakaguchi, Mayumi, Yamada, Yuko, Kitamoto, Koichi, Okada, Shinichi, Kanzaki, Susumu, Namba, Noriyuki
Publicado 2020

Newly formulated GROWJECT(®) is bioequivalent to the prior GROWJECT(®) formulation and causes less injection-associated pain

por Owada, Yasuko, Asano, Yuuka, Hanada, Takashi, Yasukawa, Hidehito, Yamaoka, Mariko, Mita, Yoko, Namba, Noriyuki
Publicado 2021

The case of a patient with MIRAGE syndrome with familial dysautonomia-like symptoms

por Kawashima-Sonoyama, Yuki, Okuno, Keisuke, Dohmoto, Tomotsune, Tanase-Nakao, Kanako, Narumi, Satoshi, Namba, Noriyuki
Publicado 2021

Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations

por Kawashima-Sonoyama, Yuki, Hotsubo, Tomoyuki, Hamajima, Takashi, Hamajima, Naoki, Fujimoto, Masanobu, Namba, Noriyuki, Kanzaki, Susumu
Publicado 2022

Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss

por Kubota, Takuo, Namba, Noriyuki, Kurotobi, Shunji, Kogaki, Shigetoyo, Hirai, Haruhiko, Kitaoka, Taichi, Nakajima, Shigeo, Ozono, Keiichi
Publicado 2006

Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease

por Yasuda, Kie, Miyoshi, Yoko, Tachibana, Makiko, Namba, Noriyuki, Miki, Kazunori, Nakata, Yukiko, Takano, Toru, Ozono, Keiichi
Publicado 2017

Endocrinological and phenotype evaluation in a patient with acrodysostosis

por Ueyama, Kaoru, Namba, Noriyuki, Kitaoka, Taichi, Yamamoto, Keiko, Fujiwara, Makoto, Ohata, Yasuhisa, Kubota, Takuo, Ozono, Keiichi
Publicado 2017

An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene

por Miura, Kohji, Namba, Noriyuki, Yamamoto, Keiko, Fujiwara, Makoto, Ohata, Yasuhisa, Kitaoka, Taichi, Kubota, Takuo, Michigami, Toshimi, Ozono, Keiichi
Publicado 2013

A Japanese Male Patient with ‘Fibular Aplasia, Tibial Campomelia and Oligodactyly’: An Additional Case Report

por Kitaoka, Taichi, Namba, Noriyuki, Kim, Ji Yoo, Kubota, Takuo, Miura, Kohji, Miyoshi, Yoko, Hirai, Haruhiko, Kogo, Mikihiko, Ozono, Keiichi
Publicado 2009

Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study

por Kubota, Takuo, Fukumoto, Seiji, Cheong, Hae Il, Michigami, Toshimi, Namba, Noriyuki, Ito, Nobuaki, Tokunaga, Shin, Gibbs, Yoshimi, Ozono, Keiichi
Publicado 2020

Therapeutic Use of Oral Sodium Phosphate (Phosribbon(®) Combination Granules) in Hereditary Hypophosphatemic Rickets

por Ozono, Keiichi, Hasegawa, Yukihiro, Minagawa, Masanori, Adachi, Masanori, Namba, Noriyuki, Kazukawa, Itsuro, Kitaoka, Taichi, Asakura, Yumi, Shimura, Asami, Naito, Yuki
Publicado 2014

A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

por Kubota, Takuo, Kotani, Tomoo, Miyoshi, Yoko, Santo, Yoko, Hirai, Haruhiko, Namba, Noriyuki, Shima, Masaaki, Shimizu, Kazuo, Nakajima, Shigeo, Ozono, Keiichi
Publicado 2006

Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features

por Ono, Erina, Ariga, Masamichi, Oshima, Sakiko, Hayakawa, Mika, Imai, Masayuki, Ochiai, Yukikatsu, Mochizuki, Hiroshi, Namba, Noriyuki, Ozono, Keiichi, Miyata, Ichiro
Publicado 2016

Safety and Efficacy of Burosumab in Pediatric Patients With X-Linked Hypophosphatemia: A Phase 3/4 Open-Label Trial

por Namba, Noriyuki, Kubota, Takuo, Muroya, Koji, Tanaka, Hiroyuki, Kanematsu, Masanori, Kojima, Masahiro, Orihara, Shunichiro, Kanda, Hironori, Seino, Yoshiki, Ozono, Keiichi
Publicado 2022

Self-Administration of Burosumab in Children and Adults with X-Linked Hypophosphataemia in Two Open-Label, Single-Arm Clinical Studies

por Kubota, Takuo, Namba, Noriyuki, Tanaka, Hiroyuki, Muroya, Koji, Imanishi, Yasuo, Takeuchi, Yasuhiro, Kanematsu, Masanori, Sun, Wei, Seino, Yoshiki, Ozono, Keiichi
Publicado 2023

Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array

por Tamura, Mayuko, Isojima, Tsuyoshi, Kawashima, Minae, Yoshida, Hideki, Yamamoto, Keiko, Kitaoka, Taichi, Namba, Noriyuki, Oka, Akira, Ozono, Keiichi, Tokunaga, Katsushi, Kitanaka, Sachiko
Publicado 2015

Pheochromocytoma complicated by cyanotic congenital heart disease: a case report

por Yamamoto, Keiko, Namba, Noriyuki, Kubota, Takuo, Usui, Takeshi, Takahashi, Kunihiko, Kitaoka, Taichi, Fujiwara, Makoto, Hori, Yumiko, Kogaki, Shigetoyo, Oue, Takaharu, Morii, Eiichi, Ozono, Keiichi
Publicado 2016

Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report

por Takeyari, Shinji, Takakuwa, Satoshi, Miyata, Kei, Yamamoto, Kenichi, Nakayama, Hirofumi, Ohata, Yasuhisa, Fujiwara, Makoto, Kitaoka, Taichi, Kubota, Takuo, Namba, Noriyuki, Sakai, Norio, Ozono, Keiichi
Publicado 2019