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Hwu, Paul Wuh-Liang
258
results:
Search for persons
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Online (258)
Mediatypes
Articles (Online) (251)
Bookchapter (Online) (1)
OpenAccess-fulltext (6)
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Sorted by: Year
?
1
A pilot study of biliary atresia newborn screening using dr..:
Lee, Chee Seng
;
Ni, Yen-Hsuan
;
Chen, Huey-Ling
...
Journal of Hepatology. 77 (2022) - p. S514 , 2022
Link:
https://doi.org/10.1016/..
?
2
STIG study: real-world data of long-term outcomes of adults..:
Gutschmidt, Kristina
;
Musumeci, Olimpia
;
Díaz-Manera, Jordi
...
Journal of Neurology. 268 (2021) 7 - p. 2482-2492 , 2021
Link:
https://doi.org/10.1007/..
?
3
Improved Motor Function in Children With Aromatic L-Amino A..:
Hwu, Paul Wuh-Liang
;
Chien, Yin-Hsiu
;
Lee, Ni-Chung
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
4
Improved Motor Function in Children With Aromatic L-Amino A..:
Hwu, Paul Wuh-Liang
;
Chien, Yin-Hsiu
;
Lee, Ni-Chung
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
5
Improved Motor Function in Children With Aromatic L-Amino A..:
Chien, Yin-Hsiu
;
Hwu, Paul Wuh-Liang
;
Lee, Ni-Chung
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
6
Safety and Improved Efficacy Outcomes in Children AADC Defi..:
Hwu, Paul Wuh-Liang
;
Chien, Yin-Hsiu
;
Lee, Ni-Chung
...
Neurology. 94 (2020) 15_supplement - p. , 2020
Link:
https://doi.org/10.1212/..
?
7
Novel mutations in the mitochondrial complex I assembly gen..:
Simon, Mariella T.
;
Eftekharian, Shaya S.
;
Stover, Alexander E.
...
Molecular Genetics and Metabolism. 126 (2019) 1 - p. 53-63 , 2019
Link:
https://doi.org/10.1016/..
?
8
Late onset of symptoms in an atypical patient with the cblJ..:
Kim, Jaeseung C.
;
Lee, Ni-Chung
;
Hwu, Paul Wuh-Liang
...
Molecular Genetics and Metabolism. 107 (2012) 4 - p. 664-668 , 2012
Link:
https://doi.org/10.1016/..
?
9
STIG study: real-world data of long-term outcomes of adults..:
Gutschmidt, Kristina
;
Musumeci, Olimpia
;
Díaz-Manera, Jordi
...
https://repository.publisso.de/resource/frl:6450290. , 2021
Link:
https://repository.publi..
?
10
Novel mutations in the mitochondrial complex I assembly gen..:
Simon, Mariella T
;
Eftekharian, Shaya S
;
Stover, Alexander E
...
qt9pr0w4vz. , 2019
Link:
https://escholarship.org..
?
11
Novel mutations in the mitochondrial complex I assembly gen..:
Simon, Mariella T
;
Eftekharian, Shaya S
;
Stover, Alexander E
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7707637/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
12
Natural History of Perinatal and Infantile Hypophosphatasia..:
Whyte, Michael P.
;
Leung, Edward
;
Wilcox, William R.
...
The Journal of Pediatrics. 209 (2019) - p. 116-124.e4 , 2019
Link:
https://doi.org/10.1016/..
?
13
Genetic heterozygosity and pseudodeficiency in the Pompe di..:
Labrousse, Paul
;
Chien, Yin-Hsiu
;
Pomponio, Robert J.
...
Molecular Genetics and Metabolism. 99 (2010) 4 - p. 379-383 , 2010
Link:
https://doi.org/10.1016/..
?
14
Differences in the predominance of lysosomal and autophagic..:
Raben, Nina
;
Ralston, Evelyn
;
Chien, Yin-Hsiu
...
Molecular Genetics and Metabolism. 101 (2010) 4 - p. 324-331 , 2010
Link:
https://doi.org/10.1016/..
?
15
Natural history of perinatal and infantile hypophosphatasia..:
Whyte, Michael P
;
Leung, Edward
;
Wilcox, William R
...
Journal of Pediatrics. , 2021
Link:
http://hdl.handle.net/10..
1-15