Andreea Liana Bot
Biographic Data
| ID | 10484928 |
|---|---|
| NAME | Andreea Liana Bot |
| GIVEN NAMES | Andreea Liana |
| FAMILY NAME | Bot |
| SIGNATURE | BOT A L |
| AFFILIATIONS | Faculty of Nursing and Health Sciences, Department 2, University of Medicine and Pharmacy “Iuliu Hatieganu”, 400023 Cluj-Napoca, Romania |
| VERIFIED | No |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
ATP6V1B1-Associated Inherited Distal Renal Tubular Acidosis in Children
Inherited distal renal tubular acidosis (dRTA) is a rare but clinically significant disorder of renal acid-base regulation that frequently presents in infancy or early childhood. Among the genetic causes of autosomal recessive dRTA, mutations in the ATP6V1B1 gene are particularly important due to their association with early-onset disease and sensorineural hearing loss. Failure to recognize and treat this condition promptly can result in growth r…
The Evaluation of Serum KIM-1 in a Pediatric Cohort of Renal Transplantation—A Pilot Study
There is a strong difference for KIM-1 at 24 h postTx between the two groups, showing a high correlation between KIM-1 and the predisposition of the graft dysfunction. Further studies are needed in order to clarify the utility of these novel biomarkers in the prediction of graft survival in renal transplantation patients
No prominent works on this page.
The Evaluation of Serum KIM-1 in a Pediatric Cohort of Renal Transplantation—A Pilot Study
There is a strong difference for KIM-1 at 24 h postTx between the two groups, showing a high correlation between KIM-1 and the predisposition of the graft dysfunction. Further studies are needed in order to clarify the utility of these novel biomarkers in the prediction of graft survival in renal transplantation patients
ATP6V1B1-Associated Inherited Distal Renal Tubular Acidosis in Children
Inherited distal renal tubular acidosis (dRTA) is a rare but clinically significant disorder of renal acid-base regulation that frequently presents in infancy or early childhood. Among the genetic causes of autosomal recessive dRTA, mutations in the ATP6V1B1 gene are particularly important due to their association with early-onset disease and sensorineural hearing loss. Failure to recognize and treat this condition promptly can result in growth r…
Amino Acid Enzymes and Metabolism (1 work) · Biomedical Research and Pathophysiology (1 work) · Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 work) · Cohort (1 work) · Cohort study (1 work) · Complement system in diseases (1 work) · Diabetes Treatment and Management (1 work) · Disease (1 work) · Distal renal tubular acidosis (1 work) · Hearing loss (1 work)