Lenka Dvořáková - Concepedia

Author

Lenka Dvořáková

Also Known As

Boretius, Susann, DVOŘÁKOVÁ, Lenka, Dvorakova L, Dvořáková, Lenka, Jarmila Miklova, L Dvorakova, L Dvoráková, L Dvořáková, L. DVORAKOVA, L. Dvorakova

166

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Charles University General University Hospital in Prague Institute of Clinical and Experimental Medicine University Hospital in Motol University College London

About

Lenka Dvořáková is an author at Charles University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	21	931
2	Health Sciences	3	3	40
3	Natural Sciences	3	3	108
4	Public Health	2	2	36
5	Social Sciences	2	2	123

Lenka Dvořáková

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations Helena Poupětová, J. Ledvinová, Linda Berná, Journal of Inherited Metabolic Disease	2010	213
Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the α-galactosidase A gene in the Czech and Slovak population Robert Dobrovolný, Lenka Dvořáková, J. Ledvinová, Journal of Molecular Medicine BiologyMendelian DisorderGenetic DisorderGeneticsEleven Novel Mutations	2005	168
Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis Maria Kousi, Eija Siintola, Lenka Dvořáková, Brain GeneticsCln7/mfsd8 GeneCln7/mfsd8 MutationsPathologyDisease Gene Identification	2009	140
A consensus protocol for functional connectivity analysis in the rat brain Joanes Grandjean, Gabriel Desrosiers-Grégoire, Cynthia Anckaerts, Nature Neuroscience Brain MappingBrain OrganizationSocial SciencesRat BrainConsensus Protocol	2023	110
Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis Michael Fietz, Moeenaldeen AlSayed, Derek Burke, Molecular Genetics and Metabolism Creutzfeldt-jakob DiseaseNeurological DisorderExpert RecommendationsDiagnosisPathology	2016	97
Prosaposin deficiency and saposin B deficiency (activator‐deficient metachromatic leukodystrophy): Report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations Ladislav Kuchař, J. Ledvinová, Martin Hřebı́ček, American Journal of Medical Genetics Part A UrologySaposin B DeficiencyAutoimmune DiseaseBiochemistryProsaposin Deficiency	2009	83
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 years Helena Jahnová, Lenka Dvořáková, Hana Vlášková, Orphanet Journal of Rare Diseases	2014	70
Lethal Fetal and Early Neonatal Presentation of Adenylosuccinate Lyase Deficiency: Observation of 6 Patients in 4 Families Katharina Mouchegh, Marie Zikánová, Georg F. Hoffmann, The Journal of Pediatrics Early Neonatal PresentationPediatricsGynecologyMaternal HealthAdenylosuccinate Lyase Deficiency	2006	68
Analysis of the hybrid proline-rich protein families from seven plant species suggests rapid diversification of their sequences and expression patterns Lenka Dvořáková, Fatima Cvrčková, Lukáš Fischer BMC Genomics	2007	53
Contiguous X-chromosome Deletion Syndrome Encompassing the BTK, TIMM8A, TAF7L, and DRP2 Genes Anna Šedivá, Anna Asplund, Jan Hadač, Journal of Clinical Immunology ChromatinDevelopmental BiologyCytogeneticsGenetic DisorderGenetics	2007	42

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