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Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease

PaperCitations, authors & open-access status

Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease have?

ScholarIQcitation count

Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease has 9 citations in the OpenAlex counts ScholarIQ stores.

When was Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease published?

ScholarIQyear

Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease has 2023 year in the ScholarIQ index.

What is the open-access status of Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease?

ScholarIQoa status

Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease has gold oa status in the ScholarIQ index.

What is the DOI of Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease?

ScholarIQdoi

The DOI for Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease is on the source record.

What is the PMID of Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease?

ScholarIQpmid

The PMID for Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease is on the source record.

What is the OpenAlex record for Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease?

ScholarIQopenalex

The OpenAlex for Recent updates in therapeutic approach using tolvaptan for autosomal dominant polycystic kidney disease is on the source record.

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