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Showing items 21-30 of 171 (18 Page(s) Totally)
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| 臺大學術典藏 |
2022-07-12T01:42:46Z |
Botulinum toxin injection for medically refractory neurogenic bladder in children: A systematic review
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Wu S.-Y.; SHANG-JEN CHANG; Yang S.S.-D.; Hsu C.-K. |
| 臺大學術典藏 |
2022-03-04T06:53:44Z |
A data-mining framework for transnational healthcare system
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Shen C.-P.; Jigjidsuren C.; Dorjgochoo S.; Chen C.-H.; Chen W.-H.; Hsu C.-K.; Wu J.-M.; Hsueh C.-W.; Lai M.-S.; CHING-TING TAN; Altangerel E.; Lai F. |
| 國立成功大學 |
2022 |
Novel compound heterozygous ITGB4 mutations underlie lethal junctional epidermolysis bullosa with pyloric atresia and aplasia cutis congenita
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Hsu, C.-H.;Tu, W.-T.;Chen, P.-C.;Yu-Yun, Lee J.;Hsu, C.-K.;Chiu, T.-M. |
| 國立成功大學 |
2022 |
Taiwanese dermatological association (TDA) consensus for the management of pemphigus
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Chu, Chu C.-Y.;Lee, C.-H.;Lee, H.-E.;Cho, Y.-T.;Hsu, C.-K.;Chan, T.C.;Hsieh, S.-C.;Wei, K.-C. |
| 國立成功大學 |
2022 |
Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan
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Miyake, T.;Natsuga, K.;Umayahara, T.;Naito, S.;Yoshimoto, J.;Senoo, A.;Wang, H.-T.;Hsu, C.-K.;Yamasaki, O.;Morizane, S. |
| 國立成功大學 |
2022 |
Transcriptomic Analysis of Blaschko-Linear Psoriasis Reveals Shared and Distinct Features with Psoriasis Vulgaris
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Onoufriadis, A.;Niazi, U.;Dimitrakopoulou, K.;Reich, J.;Ainali, C.;Papanikolaou, M.;Kesidou, E.;Hsu, C.-K.;Saqi, M.;McGrath, J.A.;Reich, K. |
| 國立成功大學 |
2022 |
Monkeypox: An emerging global threat during the COVID-19 pandemic
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Lai, C.-C.;Hsu, C.-K.;Yen, M.-Y.;Lee, P.-I.;Ko, W.-C.;Hsueh, P.-R. |
| 國立成功大學 |
2022 |
Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
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Lee, Y.-R.;Lin, Y.-C.;Chang, Y.-H.;Huang, Huang H.-Y.;Hong, Y.-K.;Aala, W.J.F.;Tu, W.-T.;Tsai, M.-C.;Chou, Y.-Y.;Hsu, C.-K. |
| 國立成功大學 |
2022 |
Plasma metabolomic and lipidomic profiling highlights metabolic changes in keloid-prone individuals
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Onoufriadis, A.;Hsu, C.-K.;Hong, Y.-K.;Lin, Y.-C.;McGrath, J.A. |
| 國立成功大學 |
2022 |
Cas9-guided haplotyping of three truncation variants in autosomal recessive disease
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Natsuga, K.;Furuta, Y.;Takashima, S.;Nohara, T.;Huang, Huang H.-Y.;Shinkuma, Shinkuma S.;Nakamura, H.;Katsuda, Y.;Higashi, Higashi H.;Hsu, C.-K.;Fukushima, S.;Ujiie, H. |
Showing items 21-30 of 171 (18 Page(s) Totally)
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