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Material Type: Report
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Two cases of transplant renal artery thrombosis and spontaneous rupture caused by mucormycosisZhu, X. ; Liu, H. ; Wang, W. ; Song, S. ; Jin, M. ; Hu, X. ; Zhang, X.Transplant Infectious Disease, 2015, Vol.17 (3), p.442-448Blackwell Publishing LtdTexto completo disponível |
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Material Type: Report
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Aggravated nausea and vomiting induced by fat emulsion for hyperemesis gravidarum: A case reportZhao, B ; Li, M ; Ren, C ; Liu, X Y ; Mei, DJournal of clinical pharmacy and therapeutics, 2017, Vol.42 (5), p.618-620Texto completo disponível |
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Material Type: Report
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Measurement of the Multi-TeV Neutrino Interaction Cross-Section with IceCube Using Earth AbsorptionHill, G. C. ; Bernardini, E. ; Blot, S. ; Bretz, H.-P. ; Franckowiak, A. ; Kintscher, T. ; Kunwar, S. ; Stasik, A. ; Usner, M. ; Bagherpour, H. ; Ansseau, I. ; Meagher, K. ; Meures, T. ; O’Murchadha, A. ; Pinat, E. ; Dumm, J. P. ; Flis, S. ; Christov, A. ; Montaruli, T. ; Glüsenkamp, T. ; Kittler, T. ; Anderson, T. ; DeLaunay, J. J. ; Keivani, A. ; Turley, C. F. ; Weiss, M. J. ; Argüelles, C. ; Collin, G. H. ; Rädel, L. ; Sälzer, T. ; Schumacher, L. ; Vehring, M. ; Wiebusch, C. H. ; Bai, X. ; Barron, J. P. ; Giang, W. ; Nowicki, S. C. ; Sarkar, S. ; Yanez, J. P. ; Yodh, G. ; Momenté, G. ; Woschnagg, K. ; Tjus, J. Becker ; Kroll, M. ; Tenholt, F. ; Becker, K.-H. ; Bindig, D. ; Helbing, K. ; Hickford, S. ; Lauber, F. ; Naumann, U. ; BenZvi, S. ; Cross, R. ; Felde, J. ; Friedman, E. ; Sullivan, G. W. ; Tatar, J. ; Meier, M. ; Rhode, W. ; Dujmovic, H. ; Jeong, M. ; Chirkin, D. ; Díaz-Vélez, J. C. ; Fahey, S. ; Griffith, Z. ; Karle, A. ; Mancina, S. ; Schneider, A. ; Wandkowsky, N. ; Wille, L. ; Casier, M. ; De Clercq, C. ; De Vries, K. D. ; De Wasseige, G. ; Kunnen, J. ; Krings, K. ; Resconi, E. ; Turcati, A. ; DeYoung, T. ; Mahn, K. B. M. ; Gaisser, T. K. ; Stanev, T. ; Tilav, S. ; De Ridder, S. ; Van Driessche, W. ; Vraeghe, M. ; Hebecker, D. ; Xu, X. W. ; Gallagher, J. ; Gerhardt, L. ; Goldschmidt, A. ; Stezelberger, T. ; Ishihara, A. ; Mase, K. ; Kohnen, G. ; Nakarmi, P. ; Pepper, J. A. ; Richman, M. ; Wills, L. ; Taboada, I.Deutsches Elektronen-Synchrotron, DESY, Hamburg 2017Texto completo disponível |
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Material Type: Report
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A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosisLiu, L H ; Chen, G ; Wang, J W ; Liu, S X ; Wang, J B ; Zhou, F S ; Zhu, J ; Sun, L D ; Gao, M ; Wang, P G ; Yang, S ; Zhang, X JClinical and experimental dermatology, 2013, Vol.38 (7), p.796-798Texto completo disponível |
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Material Type: Report
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Molecular basis for the p and P(k) phenotypes in three Chinese individualsHong, X Z ; Xu, X G ; Ying, Y L ; Liu, Y ; Ma, K R ; Lan, X F ; He, J ; Zhu, F M ; Lv, H JTransfusion medicine (Oxford, England), 2013, Vol.23 (2), p.132-133Texto completo disponível |
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Material Type: Report
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Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genesLi, Q ; Liu, L H ; Chang, R X ; Pan, G B ; Chen, G ; Gao, M ; Cai, L Q ; Wang, P G ; Pimentel, J D ; Pittelkow, M R ; Yang, S ; Zhang, X JClinical and experimental dermatology, 2014, Vol.39 (2), p.225-227Texto completo disponível |
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Material Type: Report
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54-year follow-up of lumbar posterior fusion with tibial graftLiu, Michael X ; Cai, David M ; Connolly, Patrick J ; Eskander, Mark SOrthopedics, 2011, Vol.34 (11), p.838-839Texto completo disponível |
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Material Type: Report
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Pilar leiomyoma with cytological atypia: cutaneous counterpart of atypical uterine leiomyoma?Wang, J-Y ; Liu, L-F ; Yan, J-L ; Mao, X-H ; Lao, L-MClinical and experimental dermatology, 2010, Vol.35 (5), p.550-551Texto completo disponível |
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Material Type: Report
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MRD analysis and treatment outcome in three children with SET-NUP214-positive hematological malignanciesLi, W-J ; Cui, L ; Gao, C ; Zhao, X-X ; Liu, S-G ; Xing, Y-P ; Zhang, R-D ; Zhang, D-W ; Wang, B ; Li, Z-G ; Wu, M-YInternational journal of laboratory hematology, 2011, Vol.33 (6), p.e25-e27Texto completo disponível |
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Material Type: Report
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A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese familyWang, W ; Liu, L H ; Chen, G ; Gao, M ; Zhu, J ; Zhou, F S ; Cheng, H ; Tang, H Y ; Wu, B Y ; Sun, L D ; Yang, S ; Wang, P G ; Zhang, X JClinical and experimental dermatology, 2012, Vol.37 (8), p.919-921Texto completo disponível |