Kveta Blahova

Kveta Blahova

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Kveta Blahova

Kveta Blahova

Publications by authors named "Kveta Blahova"

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14Publications

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

Eur J Pediatr 2018 Dec 24;177(12):1837-1844. Epub 2018 Sep 24.

Department of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.

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http://dx.doi.org/10.1007/s00431-018-3255-2DOI Listing
December 2018

For Debate: The Significance of Etiologic Diagnosis in Neonates with Overgrowth Syndromes. Lesson Learned from the Simpson-Golabi-Behmel Syndrome.

Pediatr Endocrinol Rev 2018 Sep;16(1):171-177

Department of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic.

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http://dx.doi.org/10.17458/per.vol16.2018.pen.fd.etiologicneonatesDOI Listing
September 2018

Attack of the clones: whole genome-based characterization of two closely related enterohemorrhagic Escherichia coli O26 epidemic lineages.

BMC Genomics 2018 Aug 31;19(1):647. Epub 2018 Aug 31.

Department of Medical Microbiology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.

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http://dx.doi.org/10.1186/s12864-018-5045-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119250PMC
August 2018

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

Eur J Pediatr 2013 Jan 22;172(1):45-9. Epub 2012 Sep 22.

Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.

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http://dx.doi.org/10.1007/s00431-012-1818-1DOI Listing
January 2013

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.

Eur J Pediatr 2012 Jan 26;171(1):121-4. Epub 2011 May 26.

Department of Pediatrics, Charles University in Prague, V Úvalu 84, 150 06, Prague 5, Czech Republic.

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http://dx.doi.org/10.1007/s00431-011-1497-3DOI Listing
January 2012

Urinary transforming growth factor-β1 in children with obstructive uropathy.

Nephrology (Carlton) 2011 Aug;16(6):595-8

Department of Paediatrics, Second Medical School, Charles University Prague, University Hospital Motol, Prague, Czech Republic.

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http://dx.doi.org/10.1111/j.1440-1797.2011.01459.xDOI Listing
August 2011

Polycystic kidney and hepatic disease with mental retardation and hand anomalies in three siblings.

Pediatr Nephrol 2009 Jul 15;24(7):1409-12. Epub 2008 Nov 15.

Department of Pediatrics, Second Medical School, University Hospital Motol, Charles University Prague, V Uvalu 84, 15006, Prague, Czech Republic.

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http://dx.doi.org/10.1007/s00467-008-1049-xDOI Listing
July 2009

Genotype-phenotype correlation in children with autosomal dominant polycystic kidney disease.

Pediatr Nephrol 2009 May 5;24(5):983-9. Epub 2009 Feb 5.

Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague, University Hospital Motol, Prague, Czech Republic.

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http://link.springer.com/10.1007/s00467-008-1090-9
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http://dx.doi.org/10.1007/s00467-008-1090-9DOI Listing
May 2009

Long-term follow-up of Czech children with D+ hemolytic-uremic syndrome.

Pediatr Nephrol 2002 Jun;17(6):400-3

First Department of Pediatrics, Second Medical School, V Uvalu 84, 150 00, Prague 5, Motol, Czech Republic.

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http://link.springer.com/10.1007/s00467-002-0836-z
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http://dx.doi.org/10.1007/s00467-002-0836-zDOI Listing
June 2002