Analysis of the hybrid proline-rich protein families from seven plant species suggests rapid diversification of their sequences and expression patterns

por Dvořáková, Lenka, Cvrčková, Fatima, Fischer, Lukáš
Publicado 2007

Maternal Cardiovascular Risk Assessment 3-to-11 Years Postpartum in Relation to Previous Occurrence of Pregnancy-Related Complications

por Hromadnikova, Ilona, Kotlabova, Katerina, Dvorakova, Lenka, Krofta, Ladislav
Publicado 2019

The Prediction of Gestational Hypertension, Preeclampsia and Fetal Growth Restriction via the First Trimester Screening of Plasma Exosomal C19MC microRNAs

por Hromadnikova, Ilona, Dvorakova, Lenka, Kotlabova, Katerina, Krofta, Ladislav
Publicado 2019

Evaluation of Vascular Endothelial Function in Young and Middle-Aged Women with Respect to a History of Pregnancy, Pregnancy-Related Complications, Classical Cardiovascular Risk Fa...

por Hromadnikova, Ilona, Kotlabova, Katerina, Dvorakova, Lenka, Krofta, Ladislav
Publicado 2020

Diabetes Mellitus and Cardiovascular Risk Assessment in Mothers with a History of Gestational Diabetes Mellitus Based on Postpartal Expression Profile of MicroRNAs Associated with...

por Hromadnikova, Ilona, Kotlabova, Katerina, Dvorakova, Lenka, Krofta, Ladislav
Publicado 2020

Postnatal Expression Profile of microRNAs Associated with Cardiovascular and Cerebrovascular Diseases in Children at the Age of 3 to 11 Years in Relation to Previous Occurrence of...

por Hromadnikova, Ilona, Kotlabova, Katerina, Dvorakova, Lenka, Krofta, Ladislav, Sirc, Jan
Publicado 2019

Substantially Altered Expression Profile of Diabetes/Cardiovascular/Cerebrovascular Disease Associated microRNAs in Children Descending from Pregnancy Complicated by Gestational Di...

por Hromadnikova, Ilona, Kotlabova, Katerina, Dvorakova, Lenka, Krofta, Ladislav, Sirc, Jan
Publicado 2020

The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations

por Poupětová, Helena, Ledvinová, Jana, Berná, Linda, Dvořáková, Lenka, Kožich, Viktor, Elleder, Milan
Publicado 2010

Light sedation with short habituation time for large‐scale functional magnetic resonance imaging studies in rats

por Dvořáková, Lenka, Stenroos, Petteri, Paasonen, Ekaterina, Salo, Raimo A., Paasonen, Jaakko, Gröhn, Olli
Publicado 2022

Observational, retrospective study of a large cohort of patients with Niemann-Pick disease type C in the Czech Republic: a surprisingly stable diagnostic rate spanning almost 40 ye...

por Jahnova, Helena, Dvorakova, Lenka, Vlaskova, Hana, Hulkova, Helena, Poupetova, Helena, Hrebicek, Martin, Jesina, Pavel
Publicado 2014

Circulating heat shock protein mRNA profile in gestational hypertension, pre-eclampsia & foetal growth restriction

por Hromadnikova, Ilona, Dvorakova, Lenka, Kotlabova, Katerina, Kestlerova, Andrea, Hympanova, Lucie, Novotna, Veronika, Doucha, Jindrich, Krofta, Ladislav
Publicado 2016

Atypical CLN2 with later onset and prolonged course: a neuropathologic study showing different sensitivity of neuronal subpopulations to TPP1 deficiency

por Elleder, Milan, Dvořáková, Lenka, Stolnaja, Larisa, Vlášková, Hana, Hůlková, Helena, Druga, Rastislav, Poupětová, Helena, Košťálová, Eva, Mikuláštík, Josef
Publicado 2008

Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients

por Malinová, Věra, Poupětová, Helena, Řeboun, Martin, Dvořáková, Lenka, Reichmannová, Stella, Švandová, Ivana, Murgašová, Lenka, Kasper, David C., Magner, Martin
Publicado 2023

Clinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech Population

por Kousal, Bohdan, Hlavata, Lucia, Vlaskova, Hana, Dvorakova, Lenka, Brichova, Michaela, Dubska, Zora, Langrova, Hana, Vincent, Andrea L., Dudakova, Lubica, Liskova, Petra
Publicado 2021

The coincidence of IgA nephropathy and Fabry disease

por Maixnerová, Dita, Tesař, Vladimír, Ryšavá, Romana, Reiterová, Jana, Poupětová, Helena, Dvořáková, Lenka, Goláň, Lubor, Neprašová, Michaela, Kidorová, Jana, Merta, Miroslav, Honsová, Eva
Publicado 2013

X-Linked Adrenoleukodystrophy: Molecular and Functional Analysis of the ABCD1 Gene in Argentinean Patients

por Amorosi, Cyntia Anabel, Myskóva, Helena, Monti, Mariela Roxana, Argaraña, Carlos Enrique, Morita, Masashi, Kemp, Stephan, de Kremer, Raquel Dodelson, Dvoráková, Lenka, de Ramírez, Ana María Oller
Publicado 2012

Mucopolysaccharidosis type I in 21 Czech and Slovak patients: Mutation analysis suggests a functional importance of C-terminus of the IDUA protein

por Vazna, Alzbeta, Beesley, Clare, Berna, Linda, Stolnaja, Larisa, Myskova, Helena, Bouckova, Michaela, Vlaskova, Hana, Poupetova, Helena, Zeman, Jiri, Magner, Martin, Hlavata, Anna, Winchester, Bryan, Hrebicek, Martin, Dvorakova, Lenka
Publicado 2009

Prosaposin Deficiency and Saposin B Deficiency (Activator-Deficient Metachromatic Leukodystrophy): Report on Two Patients Detected by Analysis of Urinary Sphingolipids and Carrying...

por Kuchař, Ladislav, Ledvinová, Jana, Hřebíček, Martin, Myšková, Helena, Dvořáková, Lenka, Berná, Linda, Chrastina, Petr, Asfaw, Befekadu, Elleder, Milan, Petermöller, Margret, Mayrhofer, Heidi, Staudt, Martin, Krägeloh-Mann, Ingeborg, Paton, Barbara C, Harzer, Klaus
Publicado 2009

Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations

por Musalkova, Dita, Majer, Filip, Kuchar, Ladislav, Luksan, Ondrej, Asfaw, Befekadu, Vlaskova, Hana, Storkanova, Gabriela, Reboun, Martin, Poupetova, Helena, Jahnova, Helena, Hulkova, Helena, Ledvinova, Jana, Dvorakova, Lenka, Sikora, Jakub, Jirsa, Milan, Vanier, Marie T., Hrebicek, Martin
Publicado 2020