|
🐜
|
Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients
9 auth.
Shigeaki Suzuki,
A. Nishikawa,
M. Kuwana,
H. Nishimura,
Yurika Watanabe,
J. Nakahara,
...
Y. Hayashi,
N. Suzuki,
I. Nishino
|
7 |
2015 |
7
🐜
|
|
🐜
|
Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies
23 auth.
W. Liang,
A. Uruha,
Shigeaki Suzuki,
N. Murakami,
E. Takeshita,
Wan-Zi Chen,
Y. Jong,
Y. Endo,
H. Komaki,
T. Fujii,
...
Y. Kawano,
M. Mori-Yoshimura,
Y. Oya,
J. Xi,
Wenhua Zhu,
Chongbo Zhao,
Yurika Watanabe,
K. Ikemoto,
A. Nishikawa,
K. Hamanaka,
S. Mitsuhashi,
N. Suzuki,
I. Nishino
|
6 |
2016 |
6
🐜
|
|
🐜
|
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
23 auth.
S. Miyatake,
S. Mitsuhashi,
Y. Hayashi,
E. Purevjav,
A. Nishikawa,
E. Koshimizu,
Mikiya Suzuki,
K. Yatabe,
Yuzo Tanaka,
K. Ogata,
...
S. Kuru,
M. Shiina,
Y. Tsurusaki,
M. Nakashima,
T. Mizuguchi,
N. Miyake,
H. Saitsu,
K. Ogata,
M. Kawai,
J. Towbin,
I. Nonaka,
I. Nishino,
N. Matsumoto
|
6 |
2017 |
6
🐜
|
|
🐜
|
Sarcoplasmic MxA expression
9 auth.
A. Uruha,
A. Nishikawa,
R. Tsuburaya,
K. Hamanaka,
M. Kuwana,
Yurika Watanabe,
...
Shigeaki Suzuki,
N. Suzuki,
I. Nishino
|
6 |
2017 |
6
🐜
|
|
🦁
|
Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders
A. Nishikawa,
S. Mitsuhashi,
N. Miyata,
I. Nishino
|
5 |
2016 |
5
🦁
|
|
🦁
|
Respiratory and cardiac function in japanese patients with dysferlinopathy
18 auth.
A. Nishikawa,
M. Mori-Yoshimura,
K. Segawa,
Y. Hayashi,
Toshiaki Takahashi,
Yuko Saito,
I. Nonaka,
M. Krahn,
N. Lévy,
J. Shimizu,
...
J. Mitsui,
E. Kimura,
J. Goto,
N. Yonemoto,
M. Aoki,
I. Nishino,
Y. Oya,
M. Murata
|
4 |
2016 |
4
🦁
|
|
🐜
|
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
16 auth.
Yoshihiko Saito,
A. Nishikawa,
A. Iida,
M. Mori-Yoshimura,
Y. Oya,
A. Ishiyama,
H. Komaki,
Seigo Nakamura,
S. Fujikawa,
T. Kanda,
...
M. Yamadera,
H. Sakiyama,
S. Hayashi,
I. Nonaka,
S. Noguchi,
I. Nishino
|
4 |
2020 |
4
🐜
|
|
🐜
|
A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene
11 auth.
Keiichiro Tsunoda,
T. Yamashita,
Emi Motokura,
Yoshiaki Takahashi,
Kota Sato,
M. Takemoto,
...
N. Hishikawa,
Y. Ohta,
A. Nishikawa,
I. Nishino,
K. Abe
|
2 |
2017 |
2
🐜
|
|
🐜
|
Emery‐Dreifuss muscular dystrophy‐related myopathy with TMEM43 mutations
7 auth.
T. Mukai,
M. Mori-Yoshimura,
A. Nishikawa,
Keiichi Hokkoku,
M. Sonoo,
I. Nishino,
...
Yuji Takahashi
|
2 |
2018 |
2
🐜
|
