Hana Flogelova
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Explore the profile of Hana Flogelova including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
282
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0
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Recent Articles
1.
Flogelova H, Bouchalova K, Smakal O, Halek J, Langova K, Cizkova K
Pediatr Nephrol
. 2024 Apr;
39(9):2645-2654.
PMID: 38622348
Background: Individuals with congenital solitary functioning kidney (SFK) are at an increased risk of kidney damage. According to some studies, the risk is higher in unilateral kidney agenesis (UKA) than...
2.
Bouchalova K, Flogelova H, Horak P, Civrny J, Mlcak P, Pink R, et al.
Diagnostics (Basel)
. 2024 Feb;
14(3).
PMID: 38337774
Juvenile primary Sjögren syndrome (pSS) with renal involvement is extremely rare, reported approximately in 50 children, predominantly girls. Here, we present the first reported case of a male child with...
3.
Marlais M, Wlodkowski T, Printza N, Kronsteiner D, Krisam R, Sauer L, et al.
Am J Kidney Dis
. 2022 Jul;
81(1):119-122.
PMID: 35810826
No abstract available.
4.
Flogelova H, Karaskova E, Bouchalova K, Rohanova M, Latalova V, Tichy T, et al.
Case Rep Nephrol Dial
. 2022 Apr;
12(1):22-30.
PMID: 35433845
Patients on long-term home parenteral nutrition (HPN) occasionally develop glomerulonephritis due to chronic central venous catheter (CVC)-related infection. Most previously reported cases were membranoproliferative glomerulonephritis (MPGN). This is a case...
5.
Seifriedova Z, Flogelova H, Sarapatka J, Smakal O, Student V
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
. 2022 Feb;
166(3):243-250.
PMID: 35147136
Antenatal hydronephrosis, dilatation of the upper urinary tract (UUTD), is a common finding on prenatal ultrasound. One of the most common causes is ureteropelvic junction (UPJ) obstruction. Although such prenatally...
6.
Garam N, Cserhalmi M, Prohaszka Z, Szilagyi A, Veszeli N, Szabo E, et al.
Front Immunol
. 2021 Sep;
12:720183.
PMID: 34566977
Background: Factor H-related protein 5 (FHR-5) is a member of the complement Factor H protein family. Due to the homology to Factor H, the main complement regulator of the alternative...
7.
Garam N, Prohaszka Z, Szilagyi A, Aigner C, Schmidt A, Gaggl M, et al.
Clin Kidney J
. 2020 Apr;
13(2):225-234.
PMID: 32296528
Background: A novel data-driven cluster analysis identified distinct pathogenic patterns in C3-glomerulopathies and immune complex-mediated membranoproliferative glomerulonephritis. Our aim was to replicate these observations in an independent cohort and elucidate...
8.
Garam N, Prohaszka Z, Szilagyi A, Aigner C, Schmidt A, Gaggl M, et al.
Orphanet J Rare Dis
. 2019 Nov;
14(1):247.
PMID: 31703608
Background: Acquired or genetic abnormalities of the complement alternative pathway are the primary cause of C3glomerulopathy(C3G) but may occur in immune-complex-mediated membranoproliferative glomerulonephritis (IC-MPGN) as well. Less is known about...
9.
Lopez-Rivera E, Liu Y, Verbitsky M, Anderson B, Capone V, Otto E, et al.
N Engl J Med
. 2017 Jan;
376(8):742-754.
PMID: 28121514
Background: The DiGeorge syndrome, the most common of the microdeletion syndromes, affects multiple organs, including the heart, the nervous system, and the kidney. It is caused by deletions on chromosome...
10.
Drlik M, Flogelova H, Martin K, Jan T, Pavel Z, Oldrich S, et al.
J Pediatr Urol
. 2016 Jun;
12(4):231.e1-4.
PMID: 27349149
Introduction: Low initial differential renal function (DRF) in patients with primary non-refluxing megaureter (PNRM) is considered an indication for surgery as are an increase of dilatation and symptoms. Objective: We...