E-LIB Suche - Ergebnisse für: Piherova, Lenka

1

(Czech Association for Preventive Cardiology Expert Consens..:

Krebsová, Alice ; Kutílková, Eva ; Zoubková, Veronika...
Cor et Vasa. 65 (2023) 5 - p. 798-805 , 2023

Link: https://doi.org/10.33678..

2

Trends in SARS-CoV-2 cycle threshold values in the Czech Re..:

Musalkova, Dita ; Piherova, Lenka ; Kwasny, Ondrej...
Scientific Reports. 13 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

3

(Fukutinopathy as a rare cause of dilated cardiomyopathy an..:

Bouzková, Kateřina ; Kubánek, Miloš ; Krebsová, Alice...
Cor et Vasa. 64 (2022) 4 - p. 468-473 , 2022

Link: https://doi.org/10.33678..

4

Non-Penetrance for Ocular Phenotype in Two Individuals Carr..:

Dudakova, Lubica ; Stranecky, Viktor ; Piherova, Lenka...
Genes. 12 (2021) 5 - p. 677 , 2021

Link: https://doi.org/10.3390/..

5

Desminopathy: Novel Desmin Variants, a New Cardiac Phenotyp..:

Kubánek, Miloš ; Schimerová, Tereza ; Piherová, Lenka...
Journal of Clinical Medicine. 9 (2020) 4 - p. 937 , 2020

Link: https://doi.org/10.3390/..

6

Danon disease is an underdiagnosed cause of advanced heart ..:

Gurka, Jiri ; Piherova, Lenka ; Majer, Filip...
ESC Heart Failure. 7 (2020) 5 - p. 2534-2543 , 2020

Link: https://doi.org/10.1002/..

7

Pigmentary retinopathy can indicate the presence of pathoge..:

Kousal, Bohdan ; Majer, Filip ; Vlaskova, Hana...
Acta Ophthalmologica. 99 (2020) 1 - p. 61-68 , 2020

Link: https://doi.org/10.1111/..

8

Alu‐mediatedXq24deletion encompassingCUL4B,LAMP2,ATP1B4,TME..:

Majer, Filip ; Kousal, Bohdan ; Dusek, Petr...
American Journal of Medical Genetics Part A. 182 (2019) 1 - p. 219-223 , 2019

Link: https://doi.org/10.1002/..

9

Genetic architecture of recent-onset dilated cardiomyopathy..:

Chaloupka, Anna ; Piherova, Lenka ; Grochova, Ilga...
Biomedical Papers. 163 (2019) 4 - p. 309-317 , 2019

Link: https://doi.org/10.5507/..

10

LAMP2 exon‐copy number variations in Danon disease heterozy..:

Majer, Filip ; Piherova, Lenka ; Reboun, Martin...
American Journal of Medical Genetics Part A. 176 (2018) 11 - p. 2430-2434 , 2018

Link: https://doi.org/10.1002/..

11

Acadian variant of Fanconi syndrome is caused by mitochondr..:

Hartmannová, Hana ; Piherová, Lenka ; Tauchmannová, Kateřina...
Human Molecular Genetics. 25 (2016) 18 - p. 4062-4079 , 2016

Link: https://doi.org/10.1093/..

12

Mutations in ANTXR1 Cause GAPO Syndrome:

Stránecký, Viktor ; Hoischen, Alexander ; Hartmannová, Hana...
The American Journal of Human Genetics. 92 (2013) 5 - p. 792-799 , 2013

Link: https://doi.org/10.1016/..

13

Novel phenotype associated with OPA1 mutations?:

Tesařová, Markéta ; Stránecký, Viktor ; Kratochvílová, Hana...
Mitochondrion. 12 (2012) 5 - p. 559 , 2012

Link: https://doi.org/10.1016/..

14

Development of a human mitochondrial oligonucleotide microa..:

Čížková, Alena ; Stránecký, Viktor ; Ivánek, Robert...
BMC Genomics. 9 (2008) 1 - p. , 2008

Link: https://doi.org/10.1186/..

15

Trends in SARS-CoV-2 cycle threshold values in the Czech Re..:

Musalkova, Dita ; Piherova, Lenka ; Kwasny, Ondrej...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105352/. , 2023

Link: http://www.ncbi.nlm.nih...