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Orphanet Journal of Rare Diseases
|
August 2, 2024
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study
Xutong Zhao, Meng Yu, Wei Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
Novel GLA gene mutations in two Chinese families with classic Fabry disease
Zhao-xia Wang, Ying Zhang, Ding-fang Bu, et al.
European Journal of Pharmacology
|
October 6, 2023
The role and mechanism of TGF-β1 in the antidepressant-like effects of tetrahydrocurcumin
Yan Yang, Jianyu Yang, Tengteng Ma, et al.
Clinical Neuropathology
|
November 6, 2020
Sural biopsy to detect the axonal cytoskeleton defects in <i>KIF5A</i>-related Charcot-Marie-Tooth disease type 2
Kang Du, Lingchao Meng, He Lv, et al.
Oncology Reports
|
September 18, 2020
MicroRNA‑137 exerts protective effects on hypoxia‑induced cell injury by inhibiting autophagy/mitophagy and maintaining mitochondrial function in breast cancer stem‑like cells
Qiongying Hu, Yun Yuan, Yeke Wu, et al.
The International Journal of Neuroscience
|
November 10, 2017
Novel compound heterozygous mutations causing Kufs disease type B
Cui Wang, Hongliang Xu, Yun Yuan, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
August 19, 2014
[Leucine-rich glioma inactivated-1 protein antibody associated limbic encephalitis: one case report]
Yi-ming Zheng, Wei Sun, Zhao-xia Wang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
July 17, 2018
Late-onset hereditary sensory and autonomic neuropathy expands the phenotypic spectrum of MFN2-related diseases
Rui Wu, Jun Fu, Lingchao Meng, et al.
Neuromuscular Disorders : NMD
|
February 22, 2015
Progression and variation of fatty infiltration of the thigh muscles in Duchenne muscular dystrophy, a muscle magnetic resonance imaging study
Wenzhu Li, Yiming Zheng, Wei Zhang, et al.
Chinese Medical Journal
|
January 17, 2018
Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy
Ya-Wen Zhao, Xiu-Juan Liu, Wei Zhang, et al.
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of 55
Search research articles
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Showing results (91-100 of 544) with videos related to
Sort By:
Page
of 55
Orphanet Journal of Rare Diseases
|
August 2, 2024
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study
Xutong Zhao, Meng Yu, Wei Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
Novel GLA gene mutations in two Chinese families with classic Fabry disease
Zhao-xia Wang, Ying Zhang, Ding-fang Bu, et al.
European Journal of Pharmacology
|
October 6, 2023
The role and mechanism of TGF-β1 in the antidepressant-like effects of tetrahydrocurcumin
Yan Yang, Jianyu Yang, Tengteng Ma, et al.
Clinical Neuropathology
|
November 6, 2020
Sural biopsy to detect the axonal cytoskeleton defects in <i>KIF5A</i>-related Charcot-Marie-Tooth disease type 2
Kang Du, Lingchao Meng, He Lv, et al.
Oncology Reports
|
September 18, 2020
MicroRNA‑137 exerts protective effects on hypoxia‑induced cell injury by inhibiting autophagy/mitophagy and maintaining mitochondrial function in breast cancer stem‑like cells
Qiongying Hu, Yun Yuan, Yeke Wu, et al.
The International Journal of Neuroscience
|
November 10, 2017
Novel compound heterozygous mutations causing Kufs disease type B
Cui Wang, Hongliang Xu, Yun Yuan, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
August 19, 2014
[Leucine-rich glioma inactivated-1 protein antibody associated limbic encephalitis: one case report]
Yi-ming Zheng, Wei Sun, Zhao-xia Wang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
July 17, 2018
Late-onset hereditary sensory and autonomic neuropathy expands the phenotypic spectrum of MFN2-related diseases
Rui Wu, Jun Fu, Lingchao Meng, et al.
Neuromuscular Disorders : NMD
|
February 22, 2015
Progression and variation of fatty infiltration of the thigh muscles in Duchenne muscular dystrophy, a muscle magnetic resonance imaging study
Wenzhu Li, Yiming Zheng, Wei Zhang, et al.
Chinese Medical Journal
|
January 17, 2018
Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy
Ya-Wen Zhao, Xiu-Juan Liu, Wei Zhang, et al.
Page
of 55