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Namba, Kazunori
142
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Online (142)
Mediatypes
Articles (Online) (81)
Bookchapter (Online) (2)
OpenAccess-fulltext (59)
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?
1
Structural basis for pathogenic variants of GJB2 and hearin..:
Namba, Kazunori
;
Mutai, Hideki
;
Matsunaga, Tatsuo
.
BMC Research Notes. 17 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
2
Apoptosis of type I spiral ganglion neuron cells in Otof-mu..:
Tsuzuki, Nobuyoshi
;
Namba, Kazunori
;
Saegusa, Chika
...
Neuroscience Letters. 803 (2023) - p. 137178 , 2023
Link:
https://doi.org/10.1016/..
?
3
Novel OTOF pathogenic variant segregating with non-syndromi..:
Kuchay, Raja A.H.
;
Mir, Yaser Rafiq
;
Zeng, Xue
...
International Journal of Pediatric Otorhinolaryngology. 130 (2020) - p. 109831 , 2020
Link:
https://doi.org/10.1016/..
?
4
Homozygous EDNRB mutation in a patient with Waardenburg syn..:
Morimoto, Noriko
;
Mutai, Hideki
;
Namba, Kazunori
...
Auris Nasus Larynx. 45 (2018) 2 - p. 222-226 , 2018
Link:
https://doi.org/10.1016/..
?
5
Prevalence of TECTA mutation in patients with mid-frequency..:
Yamamoto, Nobuko
;
Mutai, Hideki
;
Namba, Kazunori
...
Orphanet Journal of Rare Diseases. 12 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
6
Clinical characteristics of a Japanese family with hearing ..:
Minami, Shujiro B.
;
Mutai, Hideki
;
Namba, Kazunori
..
Auris Nasus Larynx. 43 (2016) 6 - p. 609-613 , 2016
Link:
https://doi.org/10.1016/..
?
7
Frequency and specific characteristics of the incomplete pa..:
Kanno, Ayako
;
Mutai, Hideki
;
Namba, Kazunori
...
The Laryngoscope. 127 (2016) 7 - p. 1663-1669 , 2016
Link:
https://doi.org/10.1002/..
?
8
High prevalence of CDH23 mutations in patients with congeni..:
Mizutari, Kunio
;
Mutai, Hideki
;
Namba, Kazunori
...
Orphanet Journal of Rare Diseases. 10 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
9
A mutation in the heparin-binding site of noggin as a novel..:
Masuda, Sawako
;
Namba, Kazunori
;
Mutai, Hideki
...
Biochemical and Biophysical Research Communications. 447 (2014) 3 - p. 496-502 , 2014
Link:
https://doi.org/10.1016/..
?
10
Chronic constipation recognized as a sign of a SOX10 mutati..:
Arimoto, Yukiko
;
Namba, Kazunori
;
Nakano, Atsuko
.
Gene. 540 (2014) 2 - p. 258-262 , 2014
Link:
https://doi.org/10.1016/..
?
11
Diverse spectrum of rare deafness genes underlies early-chi..:
Mutai, Hideki
;
Suzuki, Naohiro
;
Shimizu, Atsushi
...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013
Link:
https://doi.org/10.1186/..
?
12
Moderate hearing loss associated with a novel KCNQ4 non-tru..:
Watabe, Takahisa
;
Matsunaga, Tatsuo
;
Namba, Kazunori
...
Biochemical and Biophysical Research Communications. 432 (2013) 3 - p. 475-479 , 2013
Link:
https://doi.org/10.1016/..
?
13
In silico modeling of the pore region of a KCNQ4 missense m..:
Namba, Kazunori
;
Mutai, Hideki
;
Kaneko, Hiroki
..
BMC Research Notes. 5 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
14
Epha4 controls the midline crossing and contralateral axona..:
Hashimoto, Mitsuhiro
;
Ito, Rie
;
Kitamura, Naohito
..
Journal of Comparative Neurology. 520 (2012) 8 - p. 1702-1720 , 2012
Link:
https://doi.org/10.1002/..
?
15
Close correlation between the birth date of purkinje cells ..:
Namba, Kazunori
;
Sugihara, Izumi
;
Hashimoto, Mitsuhiro
Journal of Comparative Neurology. 519 (2011) 13 - p. 2594-2614 , 2011
Link:
https://doi.org/10.1002/..
1-15