|
🐜
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Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia
16 auth.
M. Bruno,
M. Hallett,
K. Gwinn‐Hardy,
B. Sorensen,
E. Considine,
S. Tucker,
D. Lynch,
K. Mathews,
K. Swoboda,
Juliette M. Harris,
...
B. Soong,
T. Ashizawa,
J. Jankovic,
D. Renner,
Ying-Hui Fu,
L. Ptáček
|
8 |
2004 |
8
🐜
|
|
🐜
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Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
41 auth.
Hsien-yang Lee,
Yong Huang,
N. Bruneau,
P. Roll,
E. Roberson,
Mark Hermann,
Emily A Quinn,
J. Maas,
R. Edwards,
T. Ashizawa,
B. Baykan,
K. Bhatia,
S. Bressman,
M. Bruno,
E. Brunt,
...
R. Caraballo,
B. Echenne,
N. Fejerman,
S. Frucht,
C. Gurnett,
E. Hirsch,
H. Houlden,
J. Jankovic,
Wei-Ling Lee,
D. Lynch,
S. Mohammed,
U. Müller,
M. Nespeca,
D. Renner,
J. Rochette,
G. Rudolf,
S. Saiki,
B. Soong,
K. Swoboda,
S. Tucker,
N. Wood,
M. Hanna,
A. Bowcock,
P. Szepetowski,
Ying-Hui Fu,
L. Ptáček
|
7 |
2012 |
7
🐜
|
|
🐜
|
Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington's disease patients.
8 auth.
C. Chen,
Yih-Ru Wu,
M. Cheng,
Jun-Liang Liu,
Yu‐may Lee,
Po-Wei Lee,
...
B. Soong,
D. Chiu
|
7 |
2007 |
7
🐜
|
|
🐜
|
Galectin-3 is required for the microglia-mediated brain inflammation in a model of Huntington’s disease
12 auth.
Jian-Jing Siew,
Hui-Mei Chen,
Huan-Yuan Chen,
Hung-Lin Chen,
C. Chen,
B. Soong,
...
Yih-Ru Wu,
Ching-Pang Chang,
Yi-Chen Chan,
Chun-Hung Lin,
Fu-Tong Liu,
Y. Chern
|
7 |
2019 |
7
🐜
|
|
🐜
|
Clinical spectrum of Niemann‐Pick disease type C
11 auth.
J. Fink,
M. Filling-Katz,
J. Sokol,
D. Cogan,
A. Pikus,
B. Sonies,
...
B. Soong,
P. Pentchev,
M. Comly,
R. Brady,
N. Barton
|
7 |
1989 |
7
🐜
|
|
🦁
|
Spinocerebellar ataxias: an update
B. Soong,
H. Paulson
|
7 |
2007 |
7
🦁
|
|
🐢
|
Mutations in KCND3 cause spinocerebellar ataxia type 22
22 auth.
Yi-Chung Lee,
A. Durr,
K. Majczenko,
Yen‐Hua Huang,
Yu-Chao Liu,
C. Lien,
P. Tsai,
Y. Ichikawa,
J. Goto,
M. Monin,
...
Jun Z. Li,
M. Chung,
E. Mundwiller,
V. Shakkottai,
Tze-tze Liu,
C. Tesson,
Yi-Chun Lu,
A. Brice,
S. Tsuji,
M. Burmeister,
G. Stevanin,
B. Soong
|
7 |
2012 |
7
🐢
|
|
🐜
|
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
34 auth.
C. Gaspar,
C. Gaspar,
Í. Lopes-Cendes,
S. Hayes,
Jun Goto,
K. Arvidsson,
A. Dias,
A. Dias,
I. Silveira,
I. Silveira,
Patrícia Maciel,
Patrícia Maciel,
Paula Coutinho,
Manuela Lima,
Y.-X. Zhou,
...
B. Soong,
M. Watanabe,
Paola Giunti,
Giovanni Stevanin,
Olaf Riess,
Hidenao Sasaki,
Mingli Hsieh,
Garth A. Nicholson,
E. Brunt,
J. Higgins,
M. Lauritzen,
Lisbeth Tranebjærg,
V. Volpini,
N. Wood,
L. Ranum,
Shoji Tsuji,
A. Brice,
J. Sequeiros,
G. A. Rouleau
|
7 |
2001 |
7
🐜
|
|
🐬
|
Spinocerebellar ataxia type 2 presenting as familial levodopa‐responsive parkinsonism
D. Shan,
B. Soong,
Changming Sun,
S. J. Lee,
K. Liao,
R. S. Liu
|
6 |
2001 |
6
🐬
|
|
🐜
|
ATXN2 trinucleotide repeat length correlates with risk of ALS
47 auth.
W. Sproviero,
A. Shatunov,
D. Ståhl,
M. Shoai,
W. van Rheenen,
Ashley R. Jones,
S. Al-Sarraj,
P. Andersen,
N. Bonini,
F. Conforti,
P. van Damme,
H. Daoud,
M. del Mar Amador,
I. Fogh,
M. Forzan,
...
Benjamin Gaastra,
C. Gellera,
A. Gitler,
J. Hardy,
P. Fratta,
V. La Bella,
I. Le Ber,
Tim van Langenhove,
S. Lattante,
Yi-Chung Lee,
A. Malaspina,
V. Meininger,
S. Millecamps,
R. Orrell,
R. Rademakers,
W. Robberecht,
G. Rouleau,
O. Ross,
F. Salachas,
K. Sidle,
Bradley N. Smith,
B. Soong,
G. Soraru',
G. Stevanin,
E. Kabashi,
C. Troakes,
C. van Broeckhoven,
J. Veldink,
L. H. van den Berg,
C. Shaw,
J. Powell,
A. Al-Chalabi
|
6 |
2017 |
6
🐜
|
