193 results on '"Luo, Jie‑wei"'
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2. Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report
3. The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation
4. Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation
5. A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification
6. Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation
7. A correlation study between prostate necrosis rate calculated by 3D Slicer software and clinical efficacy of prostatic artery embolization, along with an analysis of predictors of clinical success after prostatic artery embolization
8. A pedigree analysis of Rotor hyperbilirubinemia combined with hepatitis B virus infection in a SLCO1B1 and SLCO1B3 gene mutations patient
9. Dimethyl fumarate ameliorates oxidative stress-induced acute kidney injury after traumatic brain injury by activating Keap1-Nrf2/HO-1 signaling pathway
10. Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis
11. Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis
12. Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency
13. Han family with essential tremor caused by the P421L variant of the TENM4 gene in China
14. A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia
15. Clinical outcomes of uterine artery embolization and experience of postoperative transvaginal fibroid expulsion: a retrospective analysis
16. Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family
17. Eucarbwenstols A–H, eight novel compounds from Eucalyptus robusta prevents MPC-5 injury via ROS modulation and regulation of mitochondrial membrane potential
18. Retrospective observation of the efficacy and safety of prostatic artery embolization combined with transurethral resection of the prostate and simple transurethral resection of the prostate in the treatment of large (> 100 mL) benign prostatic hyperplasia
19. Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription
20. Effect of superselective prostatic artery embolization on benign prostatic hyperplasia
21. Case Report: Imaging features of a new type double inferior vena cava malformation and review
22. A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1
23. Mechanism of Ziyuglycoside II-mediated Ferroptosis-related Proteins on the Proliferation and Metastasis of Human Lung Adenocarcinoma Cell Lines.
24. Clinical and imaging features of six Han patients with SAPHO syndrome.
25. Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt–Hogg–Dubé syndrome
26. Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene
27. Safety and Efficacy of Transarterial Chemoembolization Combined with Tyrosine Kinase Inhibitor and Immune Checkpoint Inhibitors for Unresectable Hepatocellular Carcinoma: A Single Center Experience
28. Eighteen cases of renal aneurysms: Clinical retrospective analysis and experience of endovascular interventional treatment
29. A clinical analysis of intestinal mucosal necrosis and exfoliation induced by superior mesenteric vein thrombosis: A case report
30. Clinical and imaging features of six Han patients with SAPHO syndrome
31. Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine
32. Case report and analysis: Behçet’s disease with lower extremity vein thrombosis and pseudoaneurysm
33. A rare concurrence of acute tubular necrosis and chronic glomerular sclerosis in a patient with wasp stings
34. Splenic Artery Embolization and Splenectomy for Spontaneous Rupture of Splenic Hemangioma and Its Imaging Features
35. Comprehensive analysis of immune ferropotosis gene on renal clear cell carcinoma: Prognosis and influence of tumor microenvironment
36. Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant
37. A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report
38. Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
39. Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation
40. Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization
41. Rare Cases of Bronchial Aneurysm and Comparison of Interventional Embolization in the Treatment of True Bronchial Aneurysm and Pseudobronchial Aneurysm
42. Analysis of Low-Density Lipoprotein Receptor Gene Mutations in A Family with Familial Hypercholesterolemia
43. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency
44. Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family
45. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations
46. Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype
47. Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis
48. Effect of superselective prostatic artery embolization on benign prostatic hyperplasia
49. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
50. TMEM45A is involved in renal fibrosis in rats by regulating Jagged1 Notch pathway
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