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Neuroscience Letters
|
February 9, 2007
Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patients
Lei Wang, Lan Yu, Guang He, et al.
Human Genetics
|
November 10, 2012
Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia
Lan Yu, Julia Wynn, Yee Him Cheung, et al.
Chinese Medical Journal
|
March 18, 2017
Clinical Auditory Phenotypes Associated with <i>GATA3</i> Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome
Li Wang, Qiong-Fen Lin, Hong-Yang Wang, et al.
Journal of Nanobiotechnology
|
March 10, 2022
Ceria-Zirconia nanoparticles reduce intracellular globotriaosylceramide accumulation and attenuate kidney injury by enhancing the autophagy flux in cellular and animal models of Fabry disease
Jong Hun An, Sang-Eun Hong, Seong-Lan Yu, et al.
Frontiers in Neurology
|
April 28, 2025
Acupuncture as adjunctive therapy for acute cerebral infarction: a randomized clinical trial
Jiang-Peng Cao, Xin-Yue Du, Xiao-Xi Liu, et al.
Plos One
|
August 14, 2014
Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss
Hongyang Wang, Yali Zhao, Yuting Yi, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
November 14, 2015
Measuring nonspecific factors in treatment: item banks that assess the healthcare experience and attitudes from the patient's perspective
Carol M Greco, Lan Yu, Kelly L Johnston, et al.
JOR Spine
|
August 21, 2025
Quantitative Sensory Testing in an Observational Cohort of Adults With Chronic Low Back Pain
Michael J Schneider, Carol M Greco, Amanda M Acevedo, et al.
Journal of Medical Genetics
|
October 12, 2012
De novo copy number variants are associated with congenital diaphragmatic hernia
Lan Yu, Julia Wynn, Lijiang Ma, et al.
Rheumatology Advances in Practice
|
November 3, 2025
Insight from convergent validity of assessment of systemic sclerosis-associated Raynaud phenomenon with nailfold capillaroscopy
Krishnasai Abhishek Madathanapalli, Areeka Memon, Manvitha Nadella, et al.
Page
of 93
Search research articles
Search
Showing results (891-900 of 921) with videos related to
Sort By:
Page
of 93
Neuroscience Letters
|
February 9, 2007
Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patients
Lei Wang, Lan Yu, Guang He, et al.
Human Genetics
|
November 10, 2012
Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia
Lan Yu, Julia Wynn, Yee Him Cheung, et al.
Chinese Medical Journal
|
March 18, 2017
Clinical Auditory Phenotypes Associated with <i>GATA3</i> Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome
Li Wang, Qiong-Fen Lin, Hong-Yang Wang, et al.
Journal of Nanobiotechnology
|
March 10, 2022
Ceria-Zirconia nanoparticles reduce intracellular globotriaosylceramide accumulation and attenuate kidney injury by enhancing the autophagy flux in cellular and animal models of Fabry disease
Jong Hun An, Sang-Eun Hong, Seong-Lan Yu, et al.
Frontiers in Neurology
|
April 28, 2025
Acupuncture as adjunctive therapy for acute cerebral infarction: a randomized clinical trial
Jiang-Peng Cao, Xin-Yue Du, Xiao-Xi Liu, et al.
Plos One
|
August 14, 2014
Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss
Hongyang Wang, Yali Zhao, Yuting Yi, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
November 14, 2015
Measuring nonspecific factors in treatment: item banks that assess the healthcare experience and attitudes from the patient's perspective
Carol M Greco, Lan Yu, Kelly L Johnston, et al.
JOR Spine
|
August 21, 2025
Quantitative Sensory Testing in an Observational Cohort of Adults With Chronic Low Back Pain
Michael J Schneider, Carol M Greco, Amanda M Acevedo, et al.
Journal of Medical Genetics
|
October 12, 2012
De novo copy number variants are associated with congenital diaphragmatic hernia
Lan Yu, Julia Wynn, Lijiang Ma, et al.
Rheumatology Advances in Practice
|
November 3, 2025
Insight from convergent validity of assessment of systemic sclerosis-associated Raynaud phenomenon with nailfold capillaroscopy
Krishnasai Abhishek Madathanapalli, Areeka Memon, Manvitha Nadella, et al.
Page
of 93