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Showing results (21-30 of 25) with videos related to

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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 4, 2018
[Clinical features and genetic variants of Dent disease in 10 children]S L Zhao, F Zhao, Y G Sha, et al.
Transplantation Proceedings|July 1, 2008
Observation of efficacy and safety of converting the calcineurin inhibitor to sirolimus in renal transplant recipients with chronic allograft nephropathyJ Chen, L Li, J Wen, et al.
Journal of Microscopy|June 5, 2014
Microscopy and microanalysis of complex nanosized strengthening precipitates in new generation commercial Al-Cu-Li alloysM J-F Guinel, N Brodusch, G Sha, et al.
The American Journal of Physiology|December 1, 1989
Distinct hemodynamic and renal effects of calcitonin gene-related peptide and calcitonin in menM P Gnaedinger, D E Uehlinger, P Weidmann, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 28, 2022
[Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ]Y G Sha, C L Wang, Z W Du, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 4, 2018
[Clinical features and genetic variants of Dent disease in 10 children]S L Zhao, F Zhao, Y G Sha, et al.
Transplantation Proceedings|July 1, 2008
Observation of efficacy and safety of converting the calcineurin inhibitor to sirolimus in renal transplant recipients with chronic allograft nephropathyJ Chen, L Li, J Wen, et al.
Journal of Microscopy|June 5, 2014
Microscopy and microanalysis of complex nanosized strengthening precipitates in new generation commercial Al-Cu-Li alloysM J-F Guinel, N Brodusch, G Sha, et al.
The American Journal of Physiology|December 1, 1989
Distinct hemodynamic and renal effects of calcitonin gene-related peptide and calcitonin in menM P Gnaedinger, D E Uehlinger, P Weidmann, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 28, 2022
[Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ]Y G Sha, C L Wang, Z W Du, et al.
Pageof 3