Fencl F - Search Results

1

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

Sibikova M, Fencl F, David J, Vondrak K, Simankova N, Balascakova M, Indrakova J, Amaratunga SA, Lebl J. Sibikova M, et al. Among authors: fencl f. Klin Padiatr. 2024 Jul;236(4):258-261. doi: 10.1055/a-2000-5339. Epub 2023 Mar 17. Klin Padiatr. 2024. PMID: 36931311 English. No abstract available.

2

Correlation between knee roentgenogram changes and clinical symptoms in osteoarthritis.

Pavelka K, Gatterová J, Pavelka K Sr, Pelítskova Z, Svarcová Z, Janousek J, Fencl F, Urbanová Z, Gollerová V, Sedlacková M, et al. Pavelka K, et al. Among authors: fencl f. Rev Rhum Mal Osteoartic. 1992 Oct;59(9):553-9. Rev Rhum Mal Osteoartic. 1992. PMID: 1494737

3

Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene.

Obermannova B, Banghova K, Sumník Z, Dvorakova HM, Betka J, Fencl F, Kolouskova S, Cinek O, Lebl J. Obermannova B, et al. Among authors: fencl f. Eur J Pediatr. 2009 May;168(5):569-73. doi: 10.1007/s00431-008-0794-y. Epub 2008 Aug 27. Eur J Pediatr. 2009. PMID: 18751724

4

Recurrence of nephrotic proteinuria in children with focal segmental glomerulosclerosis: early treatment with plasmapheresis and immunoadsorption should be associated with better prognosis.

Fencl F, Vondrák K, Rosík T, Zieg J, Chadimová M, Háček J, Dušek J, Seeman T. Fencl F, et al. Minerva Pediatr. 2016 Oct;68(5):348-54. Epub 2015 Jun 4. Minerva Pediatr. 2016. PMID: 26041001

5

McCune Albright syndrome and bilateral adrenal hyperplasia: the GNAS mutation may only be present in adrenal tissue.

Angelousi A, Fencl F, Faucz FR, Malikova J, Sumnik Z, Lebl J, Stratakis CA. Angelousi A, et al. Among authors: fencl f. Hormones (Athens). 2015 Jul-Sep;14(3):447-50. doi: 10.14310/horm.2002.1578. Hormones (Athens). 2015. PMID: 26188235 Free PMC article.

6

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

Plachý L, Elblová L, Neuman V, Fencl F, Bláhová K, Straňák Z, Lebl J, Průhová Š. Plachý L, et al. Among authors: fencl f. Pediatr Endocrinol Rev. 2018 Sep;16(1):171-177. doi: 10.17458/per.vol16.2018.pen.fd.etiologicneonates. Pediatr Endocrinol Rev. 2018. PMID: 30371035

7

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

David J, Rohanova M, Koubsky K, Gebauer R, Malcova H, Koukolska V, Stara V, Kollar M, Fencl F, Zieg J. David J, et al. Among authors: fencl f. Klin Padiatr. 2021 Jan;233(1):37-39. doi: 10.1055/a-1183-4785. Epub 2020 Jun 18. Klin Padiatr. 2021. PMID: 32557504 English. No abstract available.

8

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

David J, Fencl F. David J, et al. Among authors: fencl f. Klin Padiatr. 2021 Nov;233(6):306-307. doi: 10.1055/a-1480-7938. Epub 2021 Sep 1. Klin Padiatr. 2021. PMID: 34470065 English. No abstract available.

9

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

David J, Toni L, Fencl F, Hrdlicka R, Buksakowska I, Paulas L, Lebl J. David J, et al. Among authors: fencl f. Klin Padiatr. 2023 Jan;235(1):55-57. doi: 10.1055/a-1690-7583. Epub 2022 Feb 3. Klin Padiatr. 2023. PMID: 35114700 English. No abstract available.

10

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

Bezdicka M, Kaufman F, Krizova I, Dostalkova A, Rumlova M, Seeman T, Vondrak K, Fencl F, Zieg J, Soucek O. Bezdicka M, et al. Among authors: fencl f. Sci Rep. 2022 May 24;12(1):8704. doi: 10.1038/s41598-022-12760-x. Sci Rep. 2022. PMID: 35610319 Free PMC article.

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