| 臺大學術典藏 |
2020-03-05T03:20:08Z |
Extracorporeal membrane oxygenation for neonatal congenital diaphragmatic hernia: The initial single-center experience in Taiwan
|
Hung W.-T.; Huang S.-C.; Mazloum D.E.; Lin W.-H.; Yang H.-H.; Chou H.-C.; Wu E.-T.; Chen C.-Y.; Tsao P.-N.; Hsieh W.-S.; WEN-MING HSU; Chen Y.-S.; Lai H.-S. |
| 臺大學術典藏 |
2020-03-04T08:52:37Z |
Surgical ligation of patent ductus arteriosus in very-low-birth-weight premature infants in the neonatal intensive care unit
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Ko Y.-C.; CHUNG-I CHANG; Chiu I.-S.; Chen Y.-S.; Huang S.-C.; Hsieh W.-S. |
| 臺大學術典藏 |
2020-03-02T08:11:22Z |
Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and α-globin genes
|
Hung C.-C.;Chien S.-C.;Lin C.-Y.;Chang C.-H.;Chang Y.-F.;Jong Y.-J.;Sung-Tsang Hsieh;Hsieh W.-S.;Liu M.S.;Lin W.-L.;Lee C.-N.;Su Y.-N.; Hung C.-C.; Chien S.-C.; Lin C.-Y.; Chang C.-H.; Chang Y.-F.; Jong Y.-J.; SUNG-TSANG HSIEH; Hsieh W.-S.; Liu M.S.; Lin W.-L.; Lee C.-N.; Su Y.-N. |
| 臺大學術典藏 |
2020-03-02T03:11:06Z |
A randomized controlled trial of clinic-based and home-based interventions in comparison with usual care for preterm infants: Effects and mediators
|
Wu Y.-C.; Leng C.-H.; Hsieh W.-S.; Hsu C.-H.; Chen W.J.; SUSAN SHUR-FEN GAU; Chiu N.-C.; Yang M.-C.; Li-Jung Fang, Hsu H.-C.; Yu Y.-T.; Wu Y.-T.; Chen L.-C.; Jeng S.-F. |
| 臺大學術典藏 |
2020-02-26T09:01:10Z |
Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test
|
Su Y.-N.;Hung C.-C.;Li H.;Lee C.-N.;Cheng W.-F.;Tsao P.-N.;Chang M.-C.;Yu C.-L.;Hsieh W.-S.;Win-Li Lin;Hsu S.-M.; Su Y.-N.; Hung C.-C.; Li H.; Lee C.-N.; Cheng W.-F.; Tsao P.-N.; Chang M.-C.; Yu C.-L.; Hsieh W.-S.; Win-Li Lin; Hsu S.-M. |
| 臺大學術典藏 |
2020-02-26T09:01:05Z |
Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy
|
Hung C.-C.;Chen C.-P.;Lin S.-P.;Chien S.-C.;Lee C.-N.;Cheng W.-F.;Hsieh W.-S.;Liu M.S.;Su Y.-N.;Win-Li Lin; Hung C.-C.; Chen C.-P.; Lin S.-P.; Chien S.-C.; Lee C.-N.; Cheng W.-F.; Hsieh W.-S.; Liu M.S.; Su Y.-N.; Win-Li Lin |
| 臺大學術典藏 |
2020-02-26T09:01:03Z |
Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and α-globin genes
|
Hung C.-C.;Chien S.-C.;Lin C.-Y.;Chang C.-H.;Chang Y.-F.;Jong Y.-J.;Hsieh S.-T.;Hsieh W.-S.;Liu M.S.;Win-Li Lin;Lee C.-N.;Su Y.-N.; Hung C.-C.; Chien S.-C.; Lin C.-Y.; Chang C.-H.; Chang Y.-F.; Jong Y.-J.; Hsieh S.-T.; Hsieh W.-S.; Liu M.S.; Win-Li Lin; Lee C.-N.; Su Y.-N. |
| 臺大學術典藏 |
2020-02-26T09:01:00Z |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
|
Hung C.-C.; Lee C.-N.; Chang C.-H.; Jong Y.-J.; Chen C.-P.; Hsieh W.-S.; Su Y.-N.; Win-Li Lin |
| 臺大學術典藏 |
2020-02-26T01:37:24Z |
Associations of supported treadmill stepping with walking attainment in preterm and full-term infants
|
Luo, H.-J.; Chen, P.-S.; Hsieh, W.-S.; Lin, K.-H.; Lu, T.-W.; Chen, W.J.; Jeng, S.-F.; TUNG-WU LU |
| 臺大學術典藏 |
2020-02-24T05:13:24Z |
Ischemic gallbladder perforation in a premature infant
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Lu Y.-Y.; HONG-SHIEE LAI; Hsieh W.-S.; Hsu W.-M. |
| 臺大學術典藏 |
2020-02-24T05:12:59Z |
Extracorporeal membrane oxygenation for neonatal congenital diaphragmatic hernia: The initial single-center experience in Taiwan
|
Hung W.-T.;Huang S.-C.;Mazloum D.E.;Lin W.-H.;Yang H.-H.;Chou H.-C.;Wu E.-T.;Chen C.-Y.;Tsao P.-N.;Hsieh W.-S.;Hsu W.-M.;Chen Y.-S.;Hong-Shiee Lai; Hung W.-T.; Huang S.-C.; Mazloum D.E.; Lin W.-H.; Yang H.-H.; Chou H.-C.; Wu E.-T.; Chen C.-Y.; Tsao P.-N.; Hsieh W.-S.; Hsu W.-M.; Chen Y.-S.; HONG-SHIEE LAI |
| 臺大學術典藏 |
2020-02-17T07:43:39Z |
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome
|
Lin S.-Y; Lee C.-N; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; Niu D.-M; Hsu W.-M; Chen L.-Y; Fang M.-Y; Tu M.-P; Kuo P.-W; Lin C.-Y; Su Y.-N; HONG-NERNG HO |
| 臺大學術典藏 |
2020-02-17T07:43:36Z |
A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
|
Lin S.-Y; Hsieh S.-C; Lin Y.-C; Lee C.-N; Tsai M.-H; Lai L.-C; Chuang E.Y; Chen P.-C; Hung C.-C; Chen L.-Y; Hsieh W.S; Niu D.-M; Su Y.-N; HONG-NERNG HO |
| 臺大學術典藏 |
2020-02-14T05:49:36Z |
Group B streptococcus antimicrobial resistance in neonates born to group B streptococcus-colonized mothers: Single-center survey
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Li Y.-P; Kuok C.-M; Lin S.-Y; Hsieh W.-S; MING-KWANG SHYU |
| 臺大學術典藏 |
2020-02-14T02:50:15Z |
Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test
|
WEN-FANG CHENG; Tsao P.-N.; Chang M.-C.; Yu C.-L.; Hsieh W.-S.; Lin W.-L.; Hsu S.-M.; Lee C.-N.; Li H.; Hung C.-C.; Su Y.-N.; Su Y.-N.;Hung C.-C.;Li H.;Lee C.-N.;Wen-Fang Cheng;Tsao P.-N.;Chang M.-C.;Yu C.-L.;Hsieh W.-S.;Lin W.-L.;Hsu S.-M. |
| 臺大學術典藏 |
2020-02-14T02:50:08Z |
Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy
|
Lin W.-L.; Su Y.-N.; Liu M.S.; Hsieh W.-S.; WEN-FANG CHENG; Lee C.-N.; Chien S.-C.; Lin S.-P.; Chen C.-P.; Hung C.-C.; Hung C.-C.;Chen C.-P.;Lin S.-P.;Chien S.-C.;Lee C.-N.;Wen-Fang Cheng;Hsieh W.-S.;Liu M.S.;Su Y.-N.;Lin W.-L. |
| 臺大學術典藏 |
2020-02-12T04:06:34Z |
Placenta Growth Factor Elevation in the Cord Blood of Premature Neonates Predicts Poor Pulmonary Outcome
|
Hsieh F.-J.;Hsieh W.-S;Chou H.-C;CHIEN-NAN LEE;Su Y.-N;Wei S.-C;Tsao P.-N; Tsao P.-N; Wei S.-C; Su Y.-N; CHIEN-NAN LEE; Chou H.-C; Hsieh W.-S; Hsieh F.-J. |
| 臺大學術典藏 |
2020-02-12T04:06:31Z |
Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test
|
Hsu S.-M.;Lin W.-L;Hsieh W.-S;Yu C.-L;Chang M.-C;Tsao P.-N;Cheng W.-F;CHIEN-NAN LEE;Li H;Hung C.-C;Su Y.-N; Su Y.-N; Hung C.-C; Li H; CHIEN-NAN LEE; Cheng W.-F; Tsao P.-N; Chang M.-C; Yu C.-L; Hsieh W.-S; Lin W.-L; Hsu S.-M. |
| 臺大學術典藏 |
2020-02-12T04:06:13Z |
Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy
|
Lin W.-L.;Su Y.-N;Liu M.S;Hsieh W.-S;Cheng W.-F;CHIEN-NAN LEE;Chien S.-C;Lin S.-P;Chen C.-P;Hung C.-C; Hung C.-C; Chen C.-P; Lin S.-P; Chien S.-C; CHIEN-NAN LEE; Cheng W.-F; Hsieh W.-S; Liu M.S; Su Y.-N; Lin W.-L. |
| 臺大學術典藏 |
2020-02-12T04:06:11Z |
Molecular assay of -�\3.7 and -�\4.2 deletions causing �\-thalassemia by denaturing high-performance liquid chromatography
|
Hsu S.-M.;Su Y.-N;Lin W.-L;Hsieh W.-S;Jong Y.-J;Chen C.-P;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chen C.-P; Jong Y.-J; Hsieh W.-S; Lin W.-L; Su Y.-N; Hsu S.-M. |
| 臺大學術典藏 |
2020-02-12T04:06:10Z |
Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and �\-globin genes
|
Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Liu M.S;Hsieh W.-S;Hsieh S.-T;Jong Y.-J;Chang Y.-F;Chang C.-H;Lin C.-Y;Chien S.-C;Hung C.-C; Hung C.-C; Chien S.-C; Lin C.-Y; Chang C.-H; Chang Y.-F; Jong Y.-J; Hsieh S.-T; Hsieh W.-S; Liu M.S; Lin W.-L; CHIEN-NAN LEE; Su Y.-N. |
| 臺大學術典藏 |
2020-02-12T04:06:08Z |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
|
Lin W.-L.;Su Y.-N;Hsieh W.-S;Chen C.-P;Jong Y.-J;Chang C.-H;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chang C.-H; Jong Y.-J; Chen C.-P; Hsieh W.-S; Su Y.-N; Lin W.-L. |
| 臺大學術典藏 |
2020-02-12T04:06:00Z |
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome
|
Ho H.-N.;Su Y.-N;Lin C.-Y;Kuo P.-W;Tu M.-P;Fang M.-Y;Chen L.-Y;Hsu W.-M;Niu D.-M;Tung Y.-C;Hsieh W.-S;Li N.-C;Lin S.-P;Tsai W.-Y;Hung C.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; Niu D.-M; Hsu W.-M; Chen L.-Y; Fang M.-Y; Tu M.-P; Kuo P.-W; Lin C.-Y; Su Y.-N; Ho H.-N. |
| 臺大學術典藏 |
2020-02-12T04:05:57Z |
Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center
|
Hsu C.-J.;Su Y.-N;CHIEN-NAN LEE;Tsao P.-N;Hsieh W.-S;Lin S.-Y;Hung C.-C;Wu C.-C; Wu C.-C; Hung C.-C; Lin S.-Y; Hsieh W.-S; Tsao P.-N; CHIEN-NAN LEE; Su Y.-N; Hsu C.-J. |
| 臺大學術典藏 |
2020-02-12T04:05:56Z |
A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
|
Ho H.-N.;Su Y.-N;Niu D.-M;Hsieh W.S;Chen L.-Y;Hung C.-C;Chen P.-C;Chuang E.Y;Lai L.-C;Tsai M.-H;CHIEN-NAN LEE;Lin Y.-C;Hsieh S.-C;Lin S.-Y; Lin S.-Y; Hsieh S.-C; Lin Y.-C; CHIEN-NAN LEE; Tsai M.-H; Lai L.-C; Chuang E.Y; Chen P.-C; Hung C.-C; Chen L.-Y; Hsieh W.S; Niu D.-M; Su Y.-N; Ho H.-N. |
