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Showing items 31-55 of 156 (7 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-07-06T02:04:16Z	Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivation	Lin M.-T.; Wang J.-K.; Yeh J.-I.; Sun L.-C.; PEI-LUNG CHEN; Wu J.-F.; Chang C.-C.; Lee W.-L.; Shen C.-T.; Wang N.-K.; Wu C.-S.; Yeh S.-Z.; Chen C.-A.; Chiu S.-N.; Wu M.-H.
臺大學術典藏	2021-07-06T02:04:15Z	Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment	Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:15Z	A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease	Lin M.-T.; Hsu C.-L.; PEI-LUNG CHEN; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H.
臺大學術典藏	2021-07-06T02:04:15Z	Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas	Wang C.-P.; Chen T.-C.; Chang Y.-L.; Ko J.-Y.; Yang T.-L.; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN; Wu C.-C.; Lou P.-J.
臺大學術典藏	2021-07-06T02:04:14Z	Tuberous sclerosis complex surveillance and management: Recommendations of the 2012 international tuberous sclerosis complex consensus conference	Krueger D.A.; Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:14Z	Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual	PEI-LUNG CHEN; Lai S.-K.; Yang W.-S.; Chang T.-C.; Chu C.-C.
臺大學術典藏	2021-07-06T02:04:13Z	Genetic analysis of CARD14 in non-familial pityriasis rubra pilaris: A case series	Hong J.-B.; PEI-LUNG CHEN; Chen Y.-T.; Tsai T.-F.
臺大學術典藏	2021-07-06T02:04:13Z	Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response	Hung C.-C.; PEI-LUNG CHEN; Huang W.-M.; Tai J.J.; Hsieh T.-J.; Ding S.-T.; Hsieh Y.-W.; Liou H.-H.
臺大學術典藏	2021-07-06T02:04:13Z	Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conference	Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:12Z	Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population	Hsieh A.-R.; Chang S.-W.; PEI-LUNG CHEN; Chu C.-C.; Hsiao C.-L.; Yang W.-S.; Chang C.-C.; Wu J.-Y.; Chen Y.-T.; Chang T.-C.; Fann C.S.J.
臺大學術典藏	2021-07-06T02:04:12Z	A fault-tolerant method for HLA typing with PacBio data	Chang C.-J.; PEI-LUNG CHEN; Yang W.-S.; Chao K.-M.
臺大學術典藏	2021-07-06T02:04:11Z	An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report	Yu T.-Y.; Lin H.-S.; PEI-LUNG CHEN; Huang T.-S.
臺大學術典藏	2021-07-06T02:04:11Z	Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing	Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:11Z	STAT3 mediates regorafenib-induced apoptosis in hepatocellular carcinoma	Tai W.-T.; Chu P.-Y.; Shiau C.-W.; Chen Y.-L.; Li Y.-S.; Hung M.-H.; Chen L.-J.; PEI-LUNG CHEN; Su J.-C.; Lin P.-Y.; Yu H.-C.; Chen K.-F.
臺大學術典藏	2021-07-06T02:04:10Z	Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling	Liu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D.
臺大學術典藏	2021-07-06T02:04:09Z	Identifying children with poor cochlear implantation outcomes using massively parallel sequencing	Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏	2021-07-06T02:04:09Z	Association between serum levels of adipocyte fatty acid-binding protein and free thyroxine	Tseng F.-Y.; PEI-LUNG CHEN; Chen Y.-T.; Chi Y.-C.; Shih S.-R.; Wang C.-Y.; Chen C.-L.; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:08Z	Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study	PEI-LUNG CHEN; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.
臺大學術典藏	2021-07-06T02:04:08Z	Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-K?ster-Hauser syndrome	Chen M.-J.; Wei S.-Y.; Yang W.-S.; Wu T.-T.; Li H.-Y.; Ho H.-N.; Yang Y.-S.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:07Z	Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer	Lin P.-H.;Kuo W.-H.;Huang A.-C.;Lu Y.-S.;Lin C.-H.;Kuo S.-H.;Wang M.-Y.;Liu C.-Y.;Cheng F.T.-F.;Yeh M.-H.;Li H.-Y.;Yang Y.-H.;Hsu Y.-H.;Fan S.-C.;Li L.-Y.;Yu S.-L.;Chang K.-J.;Pei-Lung Chen;Ni Y.-H.;Huang C.-S.; Lin P.-H.; Kuo W.-H.; Huang A.-C.; Lu Y.-S.; Lin C.-H.; Kuo S.-H.; Wang M.-Y.; Liu C.-Y.; Cheng F.T.-F.; Yeh M.-H.; Li H.-Y.; Yang Y.-H.; Hsu Y.-H.; Fan S.-C.; Li L.-Y.; Yu S.-L.; Chang K.-J.; PEI-LUNG CHEN; Ni Y.-H.; Huang C.-S.
臺大學術典藏	2021-07-06T02:04:07Z	Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations	Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:06Z	Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good 131I treatment response	Lu J.-Y.;Hung P.-J.;Pei-Lung Chen;Yen R.-F.;Kuo K.-T.;Yang T.-L.;Wang C.-Y.;Chang T.-C.;Huang T.-S.;Chang C.-C.; Lu J.-Y.; Hung P.-J.; PEI-LUNG CHEN; Yen R.-F.; Kuo K.-T.; Yang T.-L.; Wang C.-Y.; Chang T.-C.; Huang T.-S.; Chang C.-C.
臺大學術典藏	2021-07-06T02:04:06Z	Serum Spot 14 concentration is negatively associated with thyroid-stimulating hormone level	Chen Y.-T.;Tseng F.-Y.;Pei-Lung Chen;Chi Y.-C.;Han D.-S.;Yang W.-S.; Chen Y.-T.; Tseng F.-Y.; PEI-LUNG CHEN; Chi Y.-C.; Han D.-S.; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:06Z	Serum levels of follistatin are positively associated with serum-free thyroxine levels in patients with hyperthyroidism or euthyroidism	Tseng F.-Y.;Chen Y.-T.;Chi Y.-C.;Pei-Lung Chen;Yang W.-S.; Tseng F.-Y.; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:05Z	First step towards precision medicine for antithyroid drug-induced agranulocytosis	Pei-Lung Chen;Fann C.S.-J.;Shih S.-R.;Yang W.-S.;Chang T.-C.; PEI-LUNG CHEN; Fann C.S.-J.; Shih S.-R.; Yang W.-S.; Chang T.-C.

Showing items 31-55 of 156 (7 Page(s) Totally)
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