A pediatric patient with hyponatremic hypertensive syndrome without persistent hypertension in acute phase: A case report and review of literature

Authors: Nodoka Hinokuma, Shunsuke Sakurai, Atsutoshi Shiratori, Keiko Nagahara, Yoshifusa Abe, Takeshi Shimizu, Takanari Fujii, Katsumi Mizuno, Hideshi Tomita

Source: SAGE Open Medical Case Reports, Vol 8 (2020)

Subject Terms: Medicine (General), R5-920

File Description: electronic resource

Relation: https://doaj.org/toc/2050-313X

Access URL: https://doaj.org/article/95e9ed643db24ec0af9e7731384cedd0

Classification of pseudohypoaldosteronism type II as type IV renal tubular acidosis: results of a literature review.

Authors: Masanori Adachi, Sakura Motegi, Keiko Nagahara, Ayako Ochi, Junya Toyoda, Katsumi Mizuno

Source: Endocrine Journal; 2023, Vol. 70 Issue 7, p723-729, 7p

Persistent Leukocyturia Was a Clue to Diagnosis of Cystinuria in a Female Patient

Authors: Yoshifusa Abe MD, PhD, Shinichi Sakamoto MD, PhD, Eiji Morimoto, Yoshitaka Watanabe MD, Keiko Nagahara MD, PhD, Takeshi Mikawa MD, Shuichiro Watanabe MD, PhD, Kazuo Itabashi MD, PhD

Source: Global Pediatric Health, Vol 1 (2014)

Subject Terms: Pediatrics, RJ1-570

File Description: electronic resource

Relation: https://doaj.org/toc/2333-794X

Access URL: https://doaj.org/article/3286c9932f824432ae06824a628a843f

Evaluation of Phosphorylated Urinary Na-Cl Cotransporter Is Potentially Useful in a Patient With Pseudohypoaldosteronism Type II due to Mutation in

Authors: Keiko Nagahara MD, PhD, Yoshifusa Abe MD, PhD, Akira Hojo MD, Kazushige Dobashi MD, PhD, Motoko Chiga, Kiyoshi Isobe MD, PhD, Shinichi Uchida MD, PhD, Kazuo Itabashi MD, PhD

Source: Global Pediatric Health, Vol 1 (2014)

Subject Terms: Pediatrics, RJ1-570

File Description: electronic resource

Relation: https://doaj.org/toc/2333-794X

Access URL: https://doaj.org/article/47820263a93948c7aa86ddc1099c4d7a

Mutation-in-Brief: A Japanese case of familial hypercholesterolemia with a novel mutation in the LDLR gene.

Authors: Keiko Nagahara¹, Rumi Hachiya², Hayato Tada³, Hirofumi Okada³, Masakazu Yamagishi³, Kazushige Dobashi⁴, Katsumi Mizuno¹, Yukihiro Hasegawa² yhaset@gmail.com

Source: Clinical Pediatric Endocrinology. Jan2019, Vol. 28 Issue 1, p19-22. 4p. 2 Diagrams.

Subject Terms: *HYPERCHOLESTEREMIA, *GENETIC mutation, *GENES, *JAPANESE people

A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val).

Authors: Keiko Nagahara^1,2, Daisuke Ariyasu³, Junko Igaki⁴, Yuki Hasegawa⁵, Yukihiro Hasegawa¹ yhaset@gmail.com

Source: Clinical Pediatric Endocrinology. 2017, Vol. 26 Issue 4, p275-278. 4p. 1 Graph.

Subject Terms: *DIPHOSPHONATES, *PHOSPHATES, *GLYCERIN, *FRUCTOSE, *ACIDOSIS

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

Authors: Keiko Nagahara^1,2, Yuki Harada³, Tohru Futami³, Masaki Takagi^1,4, Gen Nishimura⁵, Yukihiro Hasegawa¹ yhaset@gmail.com

Source: Clinical Pediatric Endocrinology. Jul2016, Vol. 25 Issue 3, p103-106. 4p. 1 Black and White Photograph, 1 Diagram.

Subject Terms: *DWARFISM, *GROWTH disorders, *SHORT stature, *AARSKOG syndrome, *LITTLE people (Dwarfism)

Galectin-9 suppresses tumor metastasis by blocking adhesion to endothelium and extracellular matrices.

Authors: Atsuya Nobumoto, Keiko Nagahara, Souichi Oomizu, Shigeki Katoh, Nozomu Nishi, Keisuke Takeshita, Toshiro Niki, Akira Tominaga, Akira Yamauchi, Mitsuomi Hirashima

Source: Glycobiology. Sep2008, Vol. 18 Issue 9, p735-735. 1p.

Subject Terms: *CANCER cells, *METASTASIS, *CANCER invasiveness, *TUMORS