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Tanase‐Nakao, Kanako
36
results:
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Format
Online (36)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (14)
Sorted by: Relevance
Sorted by: Year
?
1
Graves' disease as an emerging complication of MIRAGE syndr..:
Wada, Tamaki
;
Mitani‐Konno, Marie
;
Tanase‐Nakao, Kanako
...
Pediatrics International. 65 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1111/..
?
2
Prevalence of germlineGATA2andSAMD9/9Lvariants in paediatri..:
Yoshida, Masanori
;
Tanase‐Nakao, Kanako
;
Shima, Hirohito
...
British Journal of Haematology. 191 (2020) 5 - p. 835-843 , 2020
Link:
https://doi.org/10.1111/..
?
3
Potential protective effect of lactation against incidence ..:
Tanase‐Nakao, Kanako
;
Arata, Naoko
;
Kawasaki, Maki
...
Diabetes/Metabolism Research and Reviews. 33 (2017) 4 - p. , 2017
Link:
https://doi.org/10.1002/..
?
4
Importance of contralateral aldosterone suppression during ..:
Umakoshi, Hironobu
;
Tanase‐Nakao, Kanako
;
Wada, Norio
...
Clinical Endocrinology. 83 (2015) 4 - p. 462-467 , 2015
Link:
https://doi.org/10.1111/..
?
5
Chronic kidney disease score for predicting postoperative m..:
Tanase‐Nakao, Kanako
;
Naruse, Mitsuhide
;
Nanba, Kazutaka
...
Clinical Endocrinology. 81 (2014) 5 - p. 665-670 , 2014
Link:
https://doi.org/10.1111/..
?
6
Concurrent THRB andDUOX2 variants in a patient detected via..:
Hatano, Megumi
;
Tanase-Nakao, Kanako
;
Uehara, Erika
...
Clinical Pediatric Endocrinology. 33 (2024) 2 - p. 94-100 , 2024
Link:
https://doi.org/10.1297/..
?
7
Genotype–Phenotype Correlations in 30 Japanese Patients Wit..:
Tanase-Nakao, Kanako
;
Iwahashi-Odano, Megumi
;
Sugisawa, Chiho
...
The Journal of Clinical Endocrinology & Metabolism. , 2024
Link:
https://doi.org/10.1210/..
?
8
Functional variants in a TTTG microsatellite on 15q26.1 cau..:
Narumi, Satoshi
;
Nagasaki, Keisuke
;
Kiriya, Mitsuo
...
Nature Genetics. 56 (2024) 5 - p. 869-876 , 2024
Link:
https://doi.org/10.1038/..
?
9
Congenital anaemia associated with loss-of-function variant..:
Takeuchi, Ichiro
;
Tanase-Nakao, Kanako
;
Ogawa, Ayame
...
Journal of Medical Genetics. , 2023
Link:
https://doi.org/10.1136/..
?
10
Novel biallelic mutations in the DUOX2 gene underlying very..:
Kyodo, Reiko
;
Takeuchi, Ichiro
;
Narumi, Satoshi
...
Clinical Immunology. 238 (2022) - p. 109015 , 2022
Link:
https://doi.org/10.1016/..
?
11
A patient with congenital hypothyroidism due to a PAX8 fram..:
Tanase-Nakao, Kanako
;
Muroya, Koji
;
Adachi, Masanori
...
Clinical Pediatric Endocrinology. 31 (2022) 4 - p. 250-255 , 2022
Link:
https://doi.org/10.1297/..
?
12
Acquired uniparental disomy of chromosome 7 in a patient wi..:
Tanase-Nakao, Kanako
;
Kawai, Masanobu
;
Wada, Kazuko
..
Clinical Pediatric Endocrinology. 30 (2021) 4 - p. 163-169 , 2021
Link:
https://doi.org/10.1297/..
?
13
A case report with functional characterization of aHNF1B mu..:
Yoshida, Kei
;
Mushimoto, Yuichi
;
Tanase-Nakao, Kanako
...
Clinical Pediatric Endocrinology. 30 (2021) 4 - p. 179-185 , 2021
Link:
https://doi.org/10.1297/..
?
14
The case of a patient with MIRAGE syndrome with familial dy..:
Kawashima-Sonoyama, Yuki
;
Okuno, Keisuke
;
Dohmoto, Tomotsune
...
Human Genome Variation. 8 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
15
MIRAGE syndrome caused by a novel missense variant (p.Ala14..:
Onuma, Shinsuke
;
Wada, Tamaki
;
Araki, Ryosuke
...
Human Genome Variation. 7 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
1-15