A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Works matching IS 17358582 AND DT 2022 AND VI 16 AND IP 3
Results: 8
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2
The Evaluation of Correlation Between Serum PTH and Dentoskeletal Changes in Panoramic Imaging of Hemodialysis Patients.
- Published in:
- 2022
- By:
- Publication type:
- journal article
3
Using Two Predictor Scoring Systems Together to Increase the Chance of Identifying the Augmented Renal Clearance Phenomenon: A Cross-sectional Study.
- Published in:
- 2022
- By:
- Publication type:
- journal article
4
Efficacy and Safety of Turmeric Dietary Supplementation on Proteinuria in CKD: A Systematic Review and Meta-analysis of RCT.
- Published in:
- 2022
- By:
- Publication type:
- journal article
5
The Association Between Plasma MicroRNA-451 Expression Levels and Chronic Kidney Disease in Children with β-Thalassemia Major.
- Published in:
- 2022
- By:
- Publication type:
- journal article
6
Clinical Course and Long-term Outcome of Adults with Primary Focal Segmental Glomerulosclerosis: A Retrospective Cohort Study.
- Published in:
- 2022
- By:
- Publication type:
- journal article
7
Evaluation of Acute Renal Failure After Acinetobacter Baumannii-related Ventilator-associated Event: Routine Data Base Study.
- Published in:
- 2022
- By:
- Publication type:
- journal article
8
Clinical Course of Patients with Bartter Syndrome.
- Published in:
- Iranian Journal of Kidney Diseases, 2022, v. 16, n. 3, p. 162, doi. 10.52547/ijkd.6657
- By:
- Publication type:
- Article