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Národný ústav detských chorôb

InstitutionResearch output, impact & collaborations

Národný ústav detských chorôb is a institution indexed in ScholarIQ from OpenAlex.

What is known about Národný ústav detských chorôb?

ScholarIQrecord summary

Národný ústav detských chorôb is a research organisation in Bratislava, SK. OpenAlex records 2,943 works and 7,748 citations for it. 733 researchers list it as their most recent affiliation.

How many works does Národný ústav detských chorôb have?

ScholarIQindexed works

Národný ústav detských chorôb has 2,943 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

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How many citations does Národný ústav detských chorôb have?

ScholarIQcitation count

Národný ústav detských chorôb has 7,748 citations in the OpenAlex counts ScholarIQ stores.

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How many researchers are at Národný ústav detských chorôb?

ScholarIQresearcher count

Národný ústav detských chorôb has 733 researchers in the ScholarIQ index.

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What is the average h-index at Národný ústav detských chorôb?

ScholarIQavg h-index

Národný ústav detských chorôb has an average h-index of 4 in OpenAlex.

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What is the ROR of Národný ústav detských chorôb?

ScholarIQror

The ROR for Národný ústav detských chorôb is on the source record.

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What is the OpenAlex record for Národný ústav detských chorôb?

ScholarIQopenalex

The OpenAlex for Národný ústav detských chorôb is on the source record.

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Who are the most-cited researchers behind Národný ústav detských chorôb?

ScholarIQtop researchers by citations

Josef Gut · Pediatric Urology and Nephrology Studies

12 works75 citations

What are the most-cited papers on Národný ústav detských chorôb?

ScholarIQmost cited works

Familial hematuria: A review

Pavlína Plevová, Josef Gut, J Janda

Medicina. 201731 CitationsOPEN ACCESS

Cerebral oedema in enuretic children during low-dose desmopressin treatment: a preventable complication

Jan Lebl, Monika Kolská, Andrea Zavacká, Jan Eliášek, Josef Gut, Jiří Biolek

European Journal of Pediatrics. 200129 Citations

A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people

Pavlína Plevová, Jana Indrakova, Judy Savige, Petra Kuhnova, Petra Tvrda, Dita Cerna, Sarka Hilscherova, Monika Kudrejova, Daniela Polendova, Radka Jaklova, Martina Langová, Helena Jahnová, Jana Laštůvková, Jiri Dusek, Josef Gut, Markéta Vlčková, Pavla Solařová, Gabriela Křečková, Eva Kantorová, Jana Šoukalová, Rastislav Slavkovský, Jana Zapletalová, Tomáš Tichý, Dana Thomasová

Frontiers in Medicine. 20236 CitationsOPEN ACCESS

Idiopathic infantile hypercalcaemia in 5-month old girl.

Josef Gut, Štěpán Kutílek

PubMed. 20115 Citations

Hematuria as symptom

Josef Gut

Pediatrie pro praxi. 20163 CitationsOPEN ACCESS

How much of the research on Národný ústav detských chorôb is open access?

ScholarIQopen access share

30%OPEN ACCESS

Gold

20%

Green

Hybrid

Bronze

10%

Closed

70%