Rongjuan H. Zhao
No.85, Jiefang South Street
Taiyuan, China
Taiyuan, China
Last Updated: 09/26/2026
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Found 17 publications
Effectiveness and pregnancy outcomes of emergency cervical cerclage versus cerclage with cervical length <10 mm: a retrospective study
Journal: Zhonghua fu chan ke za zhi
Published: February 26, 2025
Biallelic FDXR mutations induce ferroptosis in a rare mitochondrial disease with ataxia.
Journal: Free radical biology & medicine
Published: January 13, 2025
The difference of variation types between late-onset multiple acyl-CoA dehydrogenase deficiency patients carrying biallelic and single heterozygous variations in ETFDH: a systematic review and meta-analysis.
Journal: Orphanet journal of rare diseases
Published: December 17, 2024
Analysis of the pathogenicity of novel GNE mutations and clinical, pathological, and genetic characteristics of GNE myopathy in Chinese population.
Journal: Orphanet journal of rare diseases
Published: November 04, 2024
Efgartigimod versus intravenous immunoglobulin in the treatment of patients with impending myasthenic crisis.
Journal: Scientific reports
Published: September 06, 2024
The Relationship Between Ribosome-Associated Quality Control and Neurological Disorders.
Journal: The journals of gerontology. Series A, Biological sciences and medical sciences
Published: September 01, 2024
Efgartigimod in the treatment of Guillain-Barré syndrome.
Journal: Journal of neurology
Published: February 14, 2024
Relative frequencies and clinical features of Guillain-Barré Syndrome before and during the COVID-19 pandemic in North China.
Journal: BMC infectious diseases
Published: December 20, 2023
CGG Repeat Expansion in NOTCH2NLC Causing Overlapping Oculopharyngodistal Myopathy and Neuronal Intranuclear Inclusion Disease With Diffusion Weighted Imaging Abnormality in the Cerebellum.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: December 01, 2023
The male-to-female ratio in late-onset multiple acyl-CoA dehydrogenase deficiency: a systematic review and meta-analysis.
Journal: Orphanet journal of rare diseases
Published: October 19, 2023
A novel autosomal dominant ERLIN2 variant activates endoplasmic reticulum stress in a Chinese HSP family.
Journal: Annals of clinical and translational neurology
Published: March 27, 2023
Last Updated: 09/26/2026