Haiyan Wei

发表

The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening

Xuefan Gu, L. Liang, Shengnan Wu, 2022, Frontiers in Genetics.

A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia

D. Liang, Yanling Yang, Zhijun Zhu, 2020, Journal of inherited metabolic disease.

Fulminant Type 1 Diabetes in Children: A Multicenter Study in China

Qiao-zhi Yang, C. Gong, Yu-Wen Cheng, 2017, Journal of diabetes research.

ERBB3-rs2292239 as primary type 1 diabetes association locus among non-HLA genes in Chinese

W. Lu, Chengjun Sun, F. Luo, 2016, Meta gene.

Status and trends of diabetes in Chinese children: analysis of data from 14 medical centers

Jun-Fen Fu, C. Gong, Ying Xin, 2013, World Journal of Pediatrics.

An in-silico based clinical insight on the effect of noticeable CD4 conserved residues of SARS-CoV-2 on the CD4-MHC-II interactions

S. Kumar, D. Dasgupta, Haiyan Wei, 2020, bioRxiv.

Clinical efficacy of montelukast sodium combined with budesonide or combined with loratadine in treating children with cough variant asthma and influence on inflammatory factors in the serum

Haiyan Wei, Zhen Jiang, X. Xi, 2019, Experimental and therapeutic medicine.

Application of the FreeStyle®Libre Glucose Monitoring System in type 1 diabetes mellitus patients aged 1–4 years

Y. Li, B. Cao, Haiyan Wei, 2022, Pediatric diabetes.

Sirolimus Therapy and Follow-up in a Patient with Severe Congenital Hyperinsulinism Following Subtotal Pancreatectomy

Haiyan Wei, Yongxing Chen, Qiong Chen, 2020, Journal of clinical research in pediatric endocrinology.

Analysis of the Incidence and Risk Factors of Precocious Puberty in Girls during the COVID-19 Pandemic

D. Fu, B. Cao, Haiyan Wei, 2022, International journal of endocrinology.

Analysisof the IncidenceandRiskFactorsofPrecociousPuberty in Girls during the COVID-19 Pandemic

D. Fu, B. Cao, Haiyan Wei, 2022 .

A rare mutation c.1663G > A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients

Xuefan Gu, L. Liang, Shengnan Wu, 2020, Orphanet Journal of Rare Diseases.

A novel stop-loss DAX1 variant affecting its protein-interaction with SF1 precedes the adrenal hypoplasia congenital with rare spontaneous precocious puberty and an elevated hypothalamic-pituitary-gonadal/adrenal axis responses.

S. Kumar, Haiyan Wei, Yongxing Chen, 2021, European journal of medical genetics.

Epimutation of MMACHC compound to a genetic mutation in cblC cases

Yao-dong Zhang, Chongchen Zhou, Shuying Luo, 2021, Molecular genetics & genomic medicine.

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study

Yiping Shen, Linlin M Chen, D. Liang, 2022, Human mutation.

Successful treatment of vaginal and pelvic microcystic lymphatic malformations by 50% ethanol injection via lymph node angiography.

Wancun Zhang, Xianwei Zhang, Haiyan Wei, 2020, Journal of pediatric and adolescent gynecology.

A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children

Yiping Shen, J. Chen, Xiaoping Luo, 2021, The Journal of clinical endocrinology and metabolism.

Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut‐type methylmalonic acidemia: A retrospective study

Xuefan Gu, L. Liang, Shengnan Wu, 2021, Molecular genetics & genomic medicine.

Variable phenotypes and outcomes associated with the MMACHC c.609G>A homologous mutation: long term follow-up in a large cohort of cases

Yaping Tian, D. Liang, Zhehui Chen, 2020, Orphanet Journal of Rare Diseases.

Comparative docking studies to understand the binding affinity of nicotine with soluble ACE2 (sACE2)-SARS-CoV-2 complex over sACE2

S. Kumar, Haiyan Wei, S. C, 2020, Toxicology Reports.

Evaluation of clinical trials of ethnomedicine used for the treatment of diabetes: A systematic review

Avirup Chakraborty, S. Noreen, M. Abbas, 2023, Frontiers in Pharmacology.

Glutathione peroxidase 5 deficiency induces lipid metabolism regulated by reactive oxygen species in Chlamydomonas reinhardtii.

Xiaoqin Xia, Wanting Zhang, Mijuan Shi, 2020, Microbial pathogenesis.

Significance of Serum Procalcitonin Levels in Differential Diagnosis of Pediatric Pneumonia

Haiyan Wei, Weihua Li, Feng Zhu, 2015, Cell Biochemistry and Biophysics.

Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases

Xuefan Gu, L. Liang, Shengnan Wu, 2023, Journal of Medical Genetics.

Clinical, Biochemical, Molecular, and Outcome Features of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency in 10 Chinese Patients

Shengnan Wu, C. Gong, B. Cao, 2022, Frontiers in Genetics.

Clinical Study of Acute Mixed-lineage Leukemia in 14 Children

Q. Hu, Haiyan Wei, Xiao-ling Zhang, 2011, Iranian journal of pediatrics.

Clinical Studyof Acute Mixed-lineage Leukemiain14 Children

Q. Hu, Haiyan Wei, Yao-dong Zhang, 2011 .

Serum Vitamin B12 is a Promising Auxiliary Index for the Diagnosis of Methylmalonic Acidemia in Children: A Single Center Study in China.

Changlian Zhu, C. Su, Haiyan Wei, 2023, Clinica chimica acta; international journal of clinical chemistry.

Rallison syndrome due to the same mutation in EIF 2 AK 3 ( c . 205 G > T ) in two unrelated families : A case report

Haiyan Wei, Ai-xia Huang, 2022 .

A computational insight of the improved nicotine binding with ACE2-SARS-CoV-2 complex with its clinical impact

C. SelvaaKumar, S. Kumar, Haiyan Wei, 2020, 2004.14943.

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study

Yiping Shen, Linlin M Chen, D. Liang, 2021, Human mutation.