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Soong, B.W.
664
results:
Search for persons
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Format
Online (663)
Print (1)
Mediatypes
Books (1)
Articles (Online) (577)
Bookchapter (Online) (11)
OpenAccess-fulltext (75)
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english (635)
french (1)
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?
1
Age at onset prediction in spinocerebellar ataxia type 3 ch..:
de Mattos, E. P.
;
Leotti, V. B.
;
Soong, B.‐W.
...
European Journal of Neurology. 26 (2018) 1 - p. 113-120 , 2018
Link:
https://doi.org/10.1111/..
?
2
Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese..:
Jih, K.‐Y.
;
Chung, C.‐P.
;
Chang, Y.‐Y.
...
Clinical Genetics. 94 (2018) 3-4 - p. 389-390 , 2018
Link:
https://doi.org/10.1111/..
?
3
Heterozygous HTRA1 mutations in Taiwanese patients with cer..:
Liao, Y.C.
;
Chao, N.C.
;
Tsai, P.C.
..
Journal of the Neurological Sciences. 381 (2017) - p. 456 , 2017
Link:
https://doi.org/10.1016/..
?
4
A novel DNAJB6 mutation causes dominantly inherited distal‐..:
Tsai, P.‐C.
;
Tsai, Y.‐S.
;
Soong, B.‐W.
...
Clinical Genetics. 92 (2017) 2 - p. 150-157 , 2017
Link:
https://doi.org/10.1111/..
?
5
Mutations in MME cause axonal CMT in a Taiwanese cohort wit..:
Hsiao, C.T.
;
Liao, Y.C.
;
Soong, B.W.
.
Journal of the Neurological Sciences. 381 (2017) - p. 463 , 2017
Link:
https://doi.org/10.1016/..
?
6
Unmasking adrenoleukodystrophy in a cohort of cerebellar at..:
Chen, Y.H.
;
Lee, Y.C.
;
Liao, Y.C.
.
Journal of the Neurological Sciences. 381 (2017) - p. 300 , 2017
Link:
https://doi.org/10.1016/..
?
7
Investigation for SPTLC1 mutations in a Taiwanese cohort wi..:
Hsiao, C.T.
;
Chao, H.C.
;
Liao, Y.C.
...
Journal of the Neurological Sciences. 381 (2017) - p. 463-464 , 2017
Link:
https://doi.org/10.1016/..
?
8
Genetic and clinical paroxysmal kinesigenic dyskinesia in T..:
Jih, K.Y.
;
Kwan, S.Y.
;
Lee, Y.C.
...
Journal of the Neurological Sciences. 381 (2017) - p. 180 , 2017
Link:
https://doi.org/10.1016/..
?
9
3.043 HER2 POLYMORPHIC ASSOCIATION WITH PARKINSON'S DISEASE..:
Wang, V.
;
Chuang, T.-C.
;
Soong, B.-W.
..
Parkinsonism & Related Disorders. 18 (2012) - p. S179 , 2012
Link:
https://doi.org/10.1016/..
?
10
The molecular profile of NOTHC3 mutations in 21 Chinese CAD..:
Lee, Y.C.
;
Soong, B.W.
;
Liu, C.S.
Journal of the Neurological Sciences. 283 (2009) 1-2 - p. 293 , 2009
Link:
https://doi.org/10.1016/..
?
11
Population-specific spectrum of NOTCH3 mutations, MRI featu..:
Lee, Y.-C.
;
Liu, C.-S.
;
Chang, M.-H.
...
Journal of Neurology. 256 (2009) 2 - p. 249-255 , 2009
Link:
https://doi.org/10.1007/..
?
12
The 'hot cross bun' sign in the patients with spinocerebell..:
Lee, Y.‐C.
;
Liu, C.‐S.
;
Wu, H.‐M.
...
European Journal of Neurology. 16 (2009) 4 - p. 513-516 , 2009
Link:
https://doi.org/10.1111/..
?
13
MPZmutation G123S characterization: Evidence for a complex ..:
Lee, Y. C.
;
Yu, C.T.R.
;
Lin, K. P.
...
Neurology. 70 (2008) 4 - p. 273-277 , 2008
Link:
https://doi.org/10.1212/..
?
14
Regional patterns of cerebral glucose metabolism in spinoce..:
Wang, P.-S.
;
Liu, R.-S.
;
Yang, B.-H.
.
Journal of Neurology. 254 (2007) 7 - p. 838-845 , 2007
Link:
https://doi.org/10.1007/..
?
15
Spastic paraparesis as a manifestation of metabolic vitamin..:
Cheng, S.–H.
;
Chang, M.–H.
;
Soong, B.–W.
..
Journal of Neurology. 252 (2005) 9 - p. 1125-1126 , 2005
Link:
https://doi.org/10.1007/..
1-15