I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Kitanaka, Sachiko
81
results:
Search for persons
X
Format
Online (81)
Mediatypes
Articles (Online) (57)
OpenAccess-fulltext (24)
Sorted by: Relevance
Sorted by: Year
?
1
A Novel Pathogenic Variant in Fibroblast Growth Factor 23 o..:
Tanaka, Hiroyuki
;
Tamura, Mayuko
;
Muto, Mirai
...
Hormone Research in Paediatrics. , 2024
Link:
https://doi.org/10.1159/..
?
2
Clinical performance of a novel chemiluminescent enzyme imm..:
Ito, Nobuaki
;
Kubota, Takuo
;
Kitanaka, Sachiko
...
Journal of Bone and Mineral Metabolism. 39 (2021) 6 - p. 1066-1075 , 2021
Link:
https://doi.org/10.1007/..
?
3
Novel de novo MYRF gene mutation: A possible cause for seve..:
Tanaka, Hiroyuki
;
Isojima, Tsuyoshi
;
Kimura, Yuki
..
Congenital Anomalies. 61 (2020) 2 - p. 68-69 , 2020
Link:
https://doi.org/10.1111/..
?
4
Clinical and genetic characterization of nephropathy in pat..:
Harita, Yutaka
;
Urae, Seiya
;
Akashio, Riki
...
European Journal of Human Genetics. 28 (2020) 10 - p. 1414-1421 , 2020
Link:
https://doi.org/10.1038/..
?
5
Robust and highly efficient hiPSC generation from patient n..:
Okumura, Takashi
;
Horie, Yumi
;
Lai, Chen-Yi
...
Stem Cell Research & Therapy. 10 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
6
Familial dysalbuminemic hyperthyroxinemia in a 12‐year‐old ..:
Oda, Yoichiro
;
Tamura, Mayuko
;
Kitanaka, Sachiko
Pediatrics International. 61 (2019) 5 - p. 520-522 , 2019
Link:
https://doi.org/10.1111/..
?
7
Pyridoxal 5′-phosphate and related metabolites in hypophosp..:
Akiyama, Tomoyuki
;
Kubota, Takuo
;
Ozono, Keiichi
...
Molecular Genetics and Metabolism. 125 (2018) 1-2 - p. 174-180 , 2018
Link:
https://doi.org/10.1016/..
?
8
Incidence rate and characteristics of symptomatic vitamin D..:
Kubota, Takuo
;
Nakayama, Hirofumi
;
Kitaoka, Taichi
...
Endocrine Journal. 65 (2018) 6 - p. 593-599 , 2018
Link:
https://doi.org/10.1507/..
?
9
A familial case of nail patella syndrome with a heterozygou..:
Mukai, Miho
;
Fujita, Harumi
;
Umegaki-Arao, Noriko
...
Journal of Dermatological Science. 90 (2018) 1 - p. 90-93 , 2018
Link:
https://doi.org/10.1016/..
?
10
Steroid-resistant nephrotic syndrome as the initial present..:
Nakata, Tomohiro
;
Ishida, Ryo
;
Mihara, Yuu
...
BMC Nephrology. 18 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
11
Vitamin D–Deficient Rickets in Japan:
Itoh, Mitsuko
;
Tomio, Jun
;
Toyokawa, Satoshi
...
Global Pediatric Health. 4 (2017) - p. 2333794X1771134 , 2017
Link:
https://doi.org/10.1177/..
?
12
Partial monosomy of 10p and duplication of another chromoso..:
Ohta, Sayaka
;
Isojima, Tsuyoshi
;
Mizuno, Yoko
...
Pediatrics International. 59 (2017) 1 - p. 99-102 , 2017
Link:
https://doi.org/10.1111/..
?
13
Novel DHCR7 mutation in a case of Smith–Lemli–Opitz syndrom..:
Tamura, Mayuko
;
Isojima, Tsuyoshi
;
Kasama, Takeshi
...
Human Genome Variation. 4 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
14
Functional analyses of a novel missense and other mutations..:
Tamura, Mayuko
;
Ishizawa, Michiyasu
;
Isojima, Tsuyoshi
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
15
Spectrum of LMX1B mutations: from nail–patella syndrome to ..:
Harita, Yutaka
;
Kitanaka, Sachiko
;
Isojima, Tsuyoshi
..
Pediatric Nephrology. 32 (2016) 10 - p. 1845-1850 , 2016
Link:
https://doi.org/10.1007/..
1-15