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Kasagi, Yoshihiro
22
results:
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Online (22)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (9)
Sorted by: Year
Sorted by: Relevance
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1
Mastocytosis in a Case of Noonan Syndrome Caused by a De No..:
Kawaguchi, Tatsuya
;
Okanishi, Tohru
;
Okazaki, Tetsuya
...
Yonago Acta Medica. 66 (2023) 4 - p. 463-466 , 2023
Link:
https://doi.org/10.33160..
?
2
Clinical course of a Japanese patient with developmental de..:
Okazaki, Tetsuya
;
Kawaguchi, Tatsuya
;
Saiki, Yusuke
...
Human Genome Variation. 9 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
3
Clinical course of a Japanese patient with developmental de..:
Tetsuya Okazaki
;
Tatsuya Kawaguchi
;
Yusuke Saiki
...
https://doi.org/10.1038/s41439-022-00194-w. , 2022
Link:
https://doi.org/10.1038/..
?
4
Clinical course of a Japanese patient with developmental de..:
Okazaki, Tetsuya
;
Kawaguchi, Tatsuya
;
Saiki, Yusuke
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114330/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
5
Clinical course of epilepsy and white matter abnormality li..:
Okazaki, Tetsuya
;
Yamada, Hiroyuki
;
Matsuura, Kaori
...
Human Genome Variation. 8 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
6
Clinical course of epilepsy and white matter abnormality li..:
Okazaki, Tetsuya
;
Yamada, Hiroyuki
;
Matsuura, Kaori
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275604/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
7
Clinical course of epilepsy and white matter abnormality li..:
Tetsuya Okazaki
;
Hiroyuki Yamada
;
Kaori Matsuura
...
https://doi.org/10.1038/s41439-021-00157-7. , 2021
Link:
https://doi.org/10.1038/..
?
8
Duchenne muscular dystrophy–like phenotype in an LGMD2I pat..:
Okazaki, Tetsuya
;
Matsuura, Kaori
;
Kasagi, Noriko
...
Human Genome Variation. 7 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
9
Duchenne muscular dystrophy–like phenotype in an LGMD2I pat..:
Okazaki, Tetsuya
;
Matsuura, Kaori
;
Kasagi, Noriko
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171098/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
10
The evolution of surgical treatment for gastrointestinal ca..:
Maehara, Yoshihiko
;
Soejima, Yuji
;
Yoshizumi, Tomoharu
...
International Journal of Clinical Oncology. 24 (2019) 11 - p. 1333-1349 , 2019
Link:
https://doi.org/10.1007/..
?
11
Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mut..:
Okazaki, Tetsuya
;
Saito, Yoshiaki
;
Sugita, Kazunari
...
Yonago Acta Medica. 62 (2019) 1 - p. 159-162 , 2019
Link:
https://doi.org/10.33160..
?
12
Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mut..:
Okazaki, Tetsuya
;
Saito, Yoshiaki
;
Sugita, Kazunari
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437419/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
13
Clinical Diagnosis of Mendelian Disorders Using a Comprehen..:
Okazaki, Tetsuya
;
Murata, Megumi
;
Kai, Masachika
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973017/. , 2016
Link:
http://www.ncbi.nlm.nih...
?
14
The management of difficult intubation in infants: a retros..:
Aida, Junko
;
Oda, Yutaka
;
Kasagi, Yoshihiro
...
JA Clinical Reports. 1 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
15
The management of difficult intubation in infants: a retros..:
Aida, Junko
;
Oda, Yutaka
;
Kasagi, Yoshihiro
...
http://www.jaclinicalreports.com/content/1/1/18. , 2015
Link:
http://www.jaclinicalrep..
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