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Journal of Inflammation Research
|
December 13, 2024
Prediction Model and Decision Analysis for Early Recognition of SDNS/FRNS in Children
Hui Yin, Xiao Lin, Chun Gan, et al.
Cardiovascular Research
|
December 3, 2019
GHSR deficiency exacerbates cardiac fibrosis: role in macrophage inflammasome activation and myofibroblast differentiation
Mo Wang, Lei Qian, Jing Li, et al.
Frontiers in Pediatrics
|
February 27, 2023
Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases
Rui Liang, Xuelan Chen, Ying Zhang, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
August 19, 2020
Comparative Study of Endoscopic and Microscopic Type I Tympanoplasty in Terms of Delayed Facial Palsy
Kuan-Hui Li, Leong-Perng Chan, Chin-Kuo Chen, et al.
Molecular Plant Pathology
|
October 5, 2017
The major leaf ferredoxin Fd2 regulates plant innate immunity in Arabidopsis
Mo Wang, Lu Rui, Haojie Yan, et al.
BMJ (Clinical Research Ed.)
|
March 31, 2022
Psychological interventions for chronic, non-specific low back pain: systematic review with network meta-analysis
Emma Kwan-Yee Ho, Lingxiao Chen, Milena Simic, et al.
Frontiers in Pediatrics
|
April 17, 2023
Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases
Rui Liang, Xuelan Chen, Ying Zhang, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
December 21, 2006
Analysis of mastoid findings at surgery to treat middle ear cholesteatoma
Hsun-Mo Wang, Jen-Chih Lin, Ka-Wo Lee, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
July 21, 2011
Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome
Zhi-Yong Zhang, Xiao-Dong Zhao, Li-Ping Jiang, et al.
Human Immunology
|
April 12, 2015
In vivo reversion of an inherited mutation in a Chinese patient with Wiskott-Aldrich syndrome
Jing-Wen Xie, Zhi-Yong Zhang, Jun-Feng Wu, et al.
Page
of 62
Search research articles
Search
Showing results (521-530 of 620) with videos related to
Sort By:
Page
of 62
Journal of Inflammation Research
|
December 13, 2024
Prediction Model and Decision Analysis for Early Recognition of SDNS/FRNS in Children
Hui Yin, Xiao Lin, Chun Gan, et al.
Cardiovascular Research
|
December 3, 2019
GHSR deficiency exacerbates cardiac fibrosis: role in macrophage inflammasome activation and myofibroblast differentiation
Mo Wang, Lei Qian, Jing Li, et al.
Frontiers in Pediatrics
|
February 27, 2023
Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases
Rui Liang, Xuelan Chen, Ying Zhang, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
August 19, 2020
Comparative Study of Endoscopic and Microscopic Type I Tympanoplasty in Terms of Delayed Facial Palsy
Kuan-Hui Li, Leong-Perng Chan, Chin-Kuo Chen, et al.
Molecular Plant Pathology
|
October 5, 2017
The major leaf ferredoxin Fd2 regulates plant innate immunity in Arabidopsis
Mo Wang, Lu Rui, Haojie Yan, et al.
BMJ (Clinical Research Ed.)
|
March 31, 2022
Psychological interventions for chronic, non-specific low back pain: systematic review with network meta-analysis
Emma Kwan-Yee Ho, Lingxiao Chen, Milena Simic, et al.
Frontiers in Pediatrics
|
April 17, 2023
Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases
Rui Liang, Xuelan Chen, Ying Zhang, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
December 21, 2006
Analysis of mastoid findings at surgery to treat middle ear cholesteatoma
Hsun-Mo Wang, Jen-Chih Lin, Ka-Wo Lee, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
July 21, 2011
Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome
Zhi-Yong Zhang, Xiao-Dong Zhao, Li-Ping Jiang, et al.
Human Immunology
|
April 12, 2015
In vivo reversion of an inherited mutation in a Chinese patient with Wiskott-Aldrich syndrome
Jing-Wen Xie, Zhi-Yong Zhang, Jun-Feng Wu, et al.
Page
of 62