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Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children

Scientific reports, 2022-05, Vol.12 (1), p.8704-8704, Article 8704

2022

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Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis

PloS one, 2020-06, Vol.15 (6), p.e0235071-e0235071

2020

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Increasing prevalence of hypertension during long-term follow-up in children with autosomal dominant polycystic kidney disease

Pediatric nephrology (Berlin, West), 2021-11, Vol.36 (11), p.3717-3723

2021

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Life-threatening Manifestations of Vitamin B12 Deficiency in Infants on a Vegan Diet

Klinische Pädiatrie, 2021-11, Vol.233 (6), p.306-307

2021

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Blood pressure in children with renal cysts and diabetes syndrome

European journal of pediatrics, 2021-12, Vol.180 (12), p.3599-3603

2021

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Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review

Frontiers in pediatrics, 2023-06, Vol.11, p.1188098

2023

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B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)

Molecular and cellular pediatrics, 2023-10, Vol.10 (1), p.15-15, Article 15

2023

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Life-threatening Manifestations of Vitamin B12 Deficiency in Infants on a Vegan Diet

Klinische Padiatrie, 2021-11, Vol.233 (6), p.306

2021

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COVID-19-Associated Paediatric Inflammatory Multisystem Syndrome (PIMS-TS) in Intensive Care: A Retrospective Cohort Trial (PIMS-TS INT)

Children (Basel), 2023-02, Vol.10 (2), p.348

2023

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NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis

Klinische Pädiatrie, 2024-07, Vol.236 (4), p.258-261

2024

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Posterior Reversible Encephalopathy Syndrome – A Rare Complication of COVID-19 MIS-C

Klinische Pädiatrie, 2023-01, Vol.235 (1), p.55-57

2023

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Posterior Reversible Encephalopathy Syndrome - A Rare Complication of COVID-19 MIS-C

Klinische Padiatrie, 2023-01, Vol.235 (1), p.55

2023

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Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion

Journal of molecular medicine (Berlin, Germany), 2024-11, Vol.102 (11), p.1343-1353

2024

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NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis

Klinische Padiatrie, 2024-07, Vol.236 (4), p.258

2024

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Clinical characteristics of patients with a severe course of acute SARS-CoV-2 infection hospitalised in the Department of Paediatrics, University Hospital Motol

Československá pediatrie, 2022-06, Vol.77 (3), p.175-179

2022

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Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study

European journal of pediatrics, 2018-12, Vol.177 (12), p.1837-1844

2018

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A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation—a review of the literature

European journal of pediatrics, 2016-04, Vol.175 (4), p.587-592

2016

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Rhabdomyolysis in children

Pediatrie pro praxi, 2020-03, Vol.21 (1), p.17-21

2020

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Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Pediatric nephrology (Berlin, West), 2023-07, Vol.38 (7), p.2093-2100

2023

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Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria

Journal of pediatric hematology/oncology, 2023-11, Vol.45 (8), p.e1010-e1013

2023

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The Czech Home Parenteral Nutrition Registry REDNUP: Comprehensive Analysis of Adult Patients' Data

Annals of nutrition and metabolism, 2024-06, Vol.80 (3), p.143-152

2024

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Nationwide observational study of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the Czech Republic

European journal of pediatrics, 2022-10, Vol.181 (10), p.3663-3672

2022

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Case report: Anti-neutrophil Cytoplasmic Antibody-Associated Vasculitis Involving the Aortic Valve in a Twelve-year-old Girl

Klinische Padiatrie, 2021-01, Vol.233 (1), p.37-39

2021

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Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene

European journal of pediatrics, 2013, Vol.172 (1), p.45-49

2013

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Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis

Increasing prevalence of hypertension during long-term follow-up in children with autosomal dominant polycystic kidney disease

Life-threatening Manifestations of Vitamin B12 Deficiency in Infants on a Vegan Diet

Blood pressure in children with renal cysts and diabetes syndrome

Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)

Life-threatening Manifestations of Vitamin B12 Deficiency in Infants on a Vegan Diet

COVID-19-Associated Paediatric Inflammatory Multisystem Syndrome (PIMS-TS) in Intensive Care: A Retrospective Cohort Trial (PIMS-TS INT)

NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis

Posterior Reversible Encephalopathy Syndrome – A Rare Complication of COVID-19 MIS-C

Posterior Reversible Encephalopathy Syndrome - A Rare Complication of COVID-19 MIS-C

Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion

NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis

Clinical characteristics of patients with a severe course of acute SARS-CoV-2 infection hospitalised in the Department of Paediatrics, University Hospital Motol

Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study

A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation—a review of the literature

Rhabdomyolysis in children

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria

The Czech Home Parenteral Nutrition Registry REDNUP: Comprehensive Analysis of Adult Patients' Data

Nationwide observational study of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the Czech Republic

Case report: Anti-neutrophil Cytoplasmic Antibody-Associated Vasculitis Involving the Aortic Valve in a Twelve-year-old Girl

Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene

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