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Science Bulletin
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October 4, 2024
Burden of biliary tract carcinoma in China (1990-2021): Findings from the 2021 Global Burden of Disease Study
Wei Zhang, Yi-Jun Wang, Jiang-Mei Liu, et al.
Cancer Medicine
|
September 14, 2023
Improved long-term outcomes after innovative preoperative evaluation and conception of precise surgery for gallbladder cancer
Zi-Yao Jia, Yi-Di Zhu, Xiang-Song Wu, et al.
American Journal of Human Genetics
|
February 18, 2014
Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood
Clara D van Karnebeek, William S Sly, Colin J Ross, et al.
British Journal of Haematology
|
May 27, 2020
Development and validation of a prediction model (AHC) for early identification of refractory thrombotic thrombocytopenic purpura using nationally representative data
Ruo-Yun Gui, Qiu-Sha Huang, Xuan Cai, et al.
Molecular Genetics and Metabolism
|
August 2, 2016
Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families
Jörn Oliver Sass, Corinne Gemperle-Britschgi, Maja Tarailo-Graovac, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
September 9, 2017
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels
Laia Trigueros-Motos, Julian C van Capelleveen, Federico Torta, et al.
Journal of Cancer Research and Clinical Oncology
|
April 11, 2024
Oral arsenic plus imatinib versus imatinib solely for newly diagnosed chronic myeloid leukemia: a randomized phase 3 trial with 5-year outcomes
Jie Tian, Yong-Ping Song, Gao-Chong Zhang, et al.
Blood Advances
|
November 24, 2020
A risk score for predicting hospitalization for community-acquired pneumonia in ITP using nationally representative data
Ye-Jun Wu, Ming Hou, Hui-Xin Liu, et al.
Brain : a Journal of Neurology
|
December 25, 2015
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy
Irina T Zaharieva, Michael G Thor, Emily C Oates, et al.
JAMA Oncology
|
September 15, 2017
HLA-Mismatched Microtransplant in Older Patients Newly Diagnosed With Acute Myeloid Leukemia: Results From the Microtransplantation Interest Group
Mei Guo, Nelson J Chao, Jian-Yong Li, et al.
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of 81
Search research articles
Search
Showing results (791-800 of 810) with videos related to
Sort By:
Page
of 81
Science Bulletin
|
October 4, 2024
Burden of biliary tract carcinoma in China (1990-2021): Findings from the 2021 Global Burden of Disease Study
Wei Zhang, Yi-Jun Wang, Jiang-Mei Liu, et al.
Cancer Medicine
|
September 14, 2023
Improved long-term outcomes after innovative preoperative evaluation and conception of precise surgery for gallbladder cancer
Zi-Yao Jia, Yi-Di Zhu, Xiang-Song Wu, et al.
American Journal of Human Genetics
|
February 18, 2014
Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood
Clara D van Karnebeek, William S Sly, Colin J Ross, et al.
British Journal of Haematology
|
May 27, 2020
Development and validation of a prediction model (AHC) for early identification of refractory thrombotic thrombocytopenic purpura using nationally representative data
Ruo-Yun Gui, Qiu-Sha Huang, Xuan Cai, et al.
Molecular Genetics and Metabolism
|
August 2, 2016
Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families
Jörn Oliver Sass, Corinne Gemperle-Britschgi, Maja Tarailo-Graovac, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
September 9, 2017
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels
Laia Trigueros-Motos, Julian C van Capelleveen, Federico Torta, et al.
Journal of Cancer Research and Clinical Oncology
|
April 11, 2024
Oral arsenic plus imatinib versus imatinib solely for newly diagnosed chronic myeloid leukemia: a randomized phase 3 trial with 5-year outcomes
Jie Tian, Yong-Ping Song, Gao-Chong Zhang, et al.
Blood Advances
|
November 24, 2020
A risk score for predicting hospitalization for community-acquired pneumonia in ITP using nationally representative data
Ye-Jun Wu, Ming Hou, Hui-Xin Liu, et al.
Brain : a Journal of Neurology
|
December 25, 2015
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy
Irina T Zaharieva, Michael G Thor, Emily C Oates, et al.
JAMA Oncology
|
September 15, 2017
HLA-Mismatched Microtransplant in Older Patients Newly Diagnosed With Acute Myeloid Leukemia: Results From the Microtransplantation Interest Group
Mei Guo, Nelson J Chao, Jian-Yong Li, et al.
Page
of 81