Old Web
English
Sign In
Acemap
>
authorDetail
>
Atsuko Yoshizawa-Ogasawara
Atsuko Yoshizawa-Ogasawara
Boston Children's Hospital
Endocrinology
Internal medicine
Medicine
Congenital hypothyroidism
Mutation
5
Papers
53
Citations
0.00
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (5)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
SAT-295 Low Dose rFSH Prior to HCG-rFSH Therapy in Kallmann Syndrome
2019
Journal of the Endocrine Society
Atsuko Yoshizawa-Ogasawara
Toshihiro Yanai
Naoko Sato
Show All
Source
Cite
Save
Citations (0)
Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2.
2016
Journal of Pediatric Endocrinology and Metabolism
Atsuko Yoshizawa-Ogasawara
Kiyomi Abe
Sayaka Ogikubo
Satoshi Narumi
Tomonobu Hasegawa
Mari Satoh
Show All
Source
Cite
Save
Citations (9)
Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene
2015
Journal of Pediatric Endocrinology and Metabolism
Mari Satoh
Keiko Aso
Sayaka Ogikubo
Atsuko Yoshizawa-Ogasawara
Tsutomu Saji
Show All
Source
Cite
Save
Citations (21)
Third-generation Aromatase Inhibitor Improved Adult Height in a Japanese Boy with Testotoxicosis
2014
Clinical Pediatric Endocrinology
Atsuko Yoshizawa-Ogasawara
Noriyuki Katsumata
Reiko Horikawa
Mari Satoh
Tatsuhiko Urakami
Toshiaki Tanaka
Show All
Source
Cite
Save
Citations (4)
Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene
2013
Journal of Pediatric Endocrinology and Metabolism
Atsuko Yoshizawa-Ogasawara
Sayaka Ogikubo
Mari Satoh
Satoshi Narumi
Tomonobu Hasegawa
Show All
Source
Cite
Save
Citations (19)
1