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DNA diagnosis
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Mgr. Hana Vlášková
Academic staff at First Faculty of Medicine
31 publications
Publications
publication
Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.
2009 |
First Faculty of Medicine
publication
Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.
2009 |
Publication without faculty affiliation
publication
Late diagnosis of mucopolysaccharidosis type I in a girl with hand contractures
2023 |
First Faculty of Medicine
publication
Autopsy confirmed CADASIL with the c.1490C > T (p.S497L) variant of uncertain causal significance
2022 |
First Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
publication
AGAL misprocessing-induced ER stress and the unfolded protein response: lysosomal storage-independent mechanism of Fabry disease pathogenesis?
2022 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease
2021 |
First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
X-linked adrenoleukodystrophy: phenotype-genotype correlation in hemizygous males and heterozygous females with ABCD1 mutations
2021 |
First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
publication
Impact of newborn screening and early dietary management on clinical outcome of patients with long chain 3-hydroxyacyl-coa dehydrogenase deficiency and medium chain acyl-coa dehydrogenase deficiency-a retrospective nationwide study
2021 |
First Faculty of Medicine, Third Faculty of Medicine, Faculty of Mathematics and Physics
publication
Clinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech Population
2021 |
First Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Alu-mediated Xq24 deletion encompassing CUL4B, LAMP2, ATP1B4, TMEM255A, and ZBTB33 genes causes Danon disease in a female patient
2020 |
First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
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