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Gabriela Hrčková

Observed names: G Hrčková, G. Hrčková, Gabriela Hrckova
ORCID: 0000-0002-3333-7262
Observed ORCID: 0000-0002-3333-7262
OpenAlex ID: A5036523596
Prevalence of Hypertension in Children with Early-Stage ADPKD
2018 · Laura Massella, Djalila Mekahli, et al. · Clinical Journal of the American Society of Nephrology · 101
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Happle–Tinschert, Curry–Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum
2019 · M.‐L. Lovgren, Y. Zhou, et al. · British Journal of Dermatology · 15
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Genetic defects in ciliary genes in autosomal dominant polycystic kidney disease
2018 · Katarína Skalická, Gabriela Hrčková, et al. · World Journal of Nephrology · 14
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A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N‐glycans in patient's serum
2021 · Jana Ziburová, Marek Nemčovič, et al. · American Journal of Medical Genetics Part A · 12
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Myhre Syndrome Associated With Dunbar Syndrome and Urinary Tract Abnormalities: A Case Report
2020 · Zofia Varenyiova, Gabriela Hrckova, et al. · Frontiers in Pediatrics · 10
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Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus—benefit of genetic testing
2016 · Gabriela Hrčková, Viktor Jankó, et al. · European Journal of Pediatrics · 9
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension
2022 · Tomáš Seeman, Kveta Bláhová, et al. · Pediatric Nephrology · 6
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Chronic pancreatitis with polycystic kidney disease: A rare coincidence?
2019 · Gabriela Hrčková, Eszter Hegyi, et al. · Nefrología · 2
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Rare diseases and the Orphanet
2021 · Gabriela Hrčková · Neurologie pro praxi · 1
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Pancreatitis-associated chymotrypsin C (CTRC) variant p.R240Q selectively impairs trypsinogen degradation through disruption of long-range electrostatic interactions
2026 · Zoltán Attila Nagy, Máté Sándor, et al. · Scientific Reports
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Re-Evaluation of Diagnosis Glycogen Storage Disease Type 1b Based on Familiar Co-Segregation Analysis and Whole Exome Sequencing Result
2023 · Vladimir Bzduch, Katarina Skalicka, et al. · JSM Genetics & genomics.
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Tetrasomy 18p in one non-identical twin born to healthy parents: A case report
2021 · Miroslav Tomka, Gabriela Hrckova, et al. · Meta Gene
Polycystic kidneys in childhood - a wide range of overlapping diseases
2021 · Lucia Oravcová, Katarína Skalická, et al. · Urologie pro praxi
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Autozómovo recesívna polycystická choroba obličiek - Vždy iná, a predsa tá istá
2017 · G Hrčková, Z Kizeková, et al.
Works count: 14
Citation count: 170
H-index: 6
I10-index: 5
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