臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
臺大學術典藏	2021-01-04T07:38:37Z	Congenital generalized lipodystrophy in a 4-month-old infant	Lee I.-H.;Chen H.-L.;Jeng Y.-M.;Cheng M.-T.;Tsao L.-Y.;Mei-Hwei Chang; Lee I.-H.; Chen H.-L.; Jeng Y.-M.; Cheng M.-T.; Tsao L.-Y.; MEI-HWEI CHANG
臺大學術典藏	2020-12-24T06:17:06Z	Acute metabolic decompensation and sudden death in Barth syndrome: Report of a family and a literature review	Yen T.-Y.; Hwu W.-L.; YIN-HSIU CHIEN; Wu M.-H.; Lin M.-T.; Tsao L.-Y.; Hsieh W.-S.; Lee N.-C.
臺大學術典藏	2020-12-21T02:55:19Z	Acute metabolic decompensation and sudden death in Barth syndrome: Report of a family and a literature review	Lee N.-C.; Hsieh W.-S.; Yen T.-Y.; Hwu W.-L.; Chien Y.-H.; Wu M.-H.; MING-TAI LIN; Tsao L.-Y.
臺大學術典藏	2020-12-16T02:25:55Z	Acute metabolic decompensation and sudden death in Barth syndrome: Report of a family and a literature review	Yen T.-Y.;Wuh-Liang Hwu;Chien Y.-H.;Wu M.-H.;Lin M.-T.;Tsao L.-Y.;Hsieh W.-S.;Lee N.-C.; Yen T.-Y.; WUH-LIANG HWU; Chien Y.-H.; Wu M.-H.; Lin M.-T.; Tsao L.-Y.; Hsieh W.-S.; Lee N.-C.
臺大學術典藏	2020-12-09T01:38:40Z	Acute metabolic decompensation and sudden death in Barth syndrome: Report of a family and a literature review	Yen T.-Y.;Hwu W.-L.;Chien Y.-H.;Wu M.-H.;Lin M.-T.;Tsao L.-Y.;Hsieh W.-S.;Ni-Chung Lee; Yen T.-Y.; Hwu W.-L.; Chien Y.-H.; Wu M.-H.; Lin M.-T.; Tsao L.-Y.; Hsieh W.-S.; NI-CHUNG LEE
臺大學術典藏	2020-03-12T01:36:47Z	Revisit on congenital bronchopulmonary vascular malformations: A haphazard branching theory of malinosculations and its clinical classification and implication	Lee M.-L.;Tsao L.-Y.;Chaou W.-T.;Yang A.D.;Yeh K.-T.;Wang J.-K.;Wu M.-H.;Lue H.-C.;Ing-Sh Chiu;Chang C.-I.; Lee M.-L.; Tsao L.-Y.; Chaou W.-T.; Yang A.D.; Yeh K.-T.; Wang J.-K.; Wu M.-H.; Lue H.-C.; ING-SH CHIU; Chang C.-I.
臺大學術典藏	2020-03-12T01:36:46Z	Maternally inherited unbalanced translocation of chromosome 22 in a 5-day-old neonate with persistent fifth aortic arch and tetralogy of Fallot [5]	Lee M.-L.;Tsao L.-Y.;Wang B.-T.;Lee M.-H.;Ing-Sh Chiu; Lee M.-L.; Tsao L.-Y.; Wang B.-T.; Lee M.-H.; ING-SH CHIU
臺大學術典藏	2020-03-12T01:36:45Z	Revisit on a distinctive chromosome 1p36 deletion syndrome: Report of one case and review of the English literature [2]	Lee M.-L.;Tsao L.-Y.;Wang B.-T.;Lee M.-H.;Ing-Sh Chiu; Lee M.-L.; Tsao L.-Y.; Wang B.-T.; Lee M.-H.; ING-SH CHIU
臺大學術典藏	2020-03-12T01:36:43Z	Persistent fifth aortic arch associated with 22q11.2 deletion syndrome	Lee M.-L.;Chen H.-N.;Chen M.;Tsao L.-Y.;Wang B.-T.;Lee M.-H.;Ing-Sh Chiu; Lee M.-L.; Chen H.-N.; Chen M.; Tsao L.-Y.; Wang B.-T.; Lee M.-H.; ING-SH CHIU
臺大學術典藏	2020-03-12T01:36:35Z	Congenital stridor and wheezing as harbingers of the del22q11.2 syndrome presenting cardiovascular malformations of right aortic arch, aberrant left subclavian artery, Kommerell's diverticulum, and left ligamentum arteriosum	Lee M.-L.;Chen M.;Tsao L.-Y.;Chiu H.-Y.;Ing-Sh Chiu;Yang A.D.;Tsai P.-L.; Lee M.-L.; Chen M.; Tsao L.-Y.; Chiu H.-Y.; ING-SH CHIU; Yang A.D.; Tsai P.-L.

Showing items 6-15 of 26 (3 Page(s) Totally)
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