Publications by authors named "Anna Hlavata"

Claim this Profile
O
Outcome of Haemopoietic Stem Cell Transplantation in 21 Patients With Alpha-Mannosidosis.
Robert Šáhó, Renata Formánková, Julie B Eisengart, Allan Meldgaard Lund, Cecilie Videbaek

J Inherit Metab Dis· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Application of HPLC-FLD and NMR in the Monitoring of Therapy Efficacy in Alpha-Mannosidosis.
Maroš Krchňák, Rebeka Kodríková, Mária Matulová, Marek Nemčovič, Iveta Uhliariková

Front Biosci (Landmark Ed)· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fabry Disease in Slovakia: How the Situation Has Changed over 20 Years of Treatment.
Katarina Jurickova, Petra Jungova, Robert Petrovic, Slavomira Mattosova, Tereza Hlavata, Anna Hlavata

J Pers Med· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers.
Anna Tylki-Szymańska, Zsuzsanna Almássy, Violetta Christophidou-Anastasiadou, Daniela Avdjieva-Tzavella, Ingeborg Barisic, Anna Hlavata

Orphanet J Rare Dis· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum.
Jana Ziburová, Marek Nemčovič, Sergej Šesták, Jana Bellová, Zuzana Pakanová

Am J Med Genet A· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
White matter alteration and cerebellar atrophy are hallmarks of brain MRI in alpha-mannosidosis.
Jitka Majovska, Igor Nestrasil, Amy Paulson, David Nascene, Katarina Jurickova, Anna Hlavata

Mol Genet Metab· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series.
Dafne Dain Gandelman Horovitz, Angelina X Acosta, Roberto Giugliani, Anna Hlavatá, Katarína Hlavatá

Orphanet J Rare Dis· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The prevalence of melanocortin-4 receptor gene mutations in Slovak obese children and adolescents.
Emil Polák, Eva Vitáriušová, Peter Celec, Zuzana Pribilincová, Ľudmila Košťálová

J Pediatr Endocrinol Metab· January 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spectrum of GBA mutations in patients with Gaucher disease from Slovakia: identification of five novel mutations.
Slavomíra Mattošová, Ján Chandoga, Anna Hlavatá, Jana Saligová, Danka Maceková

Isr Med Assoc J· March 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Association between asymptomatic hyperuricaemia and metabolic syndrome in the adolescents].
Ivana Koborová, Radana Gurecká, Anna Hlavatá, Katarína Šebeková

Vnitr Lek· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluation of lipid and glucose metabolism and cortisol and thyroid hormone levels in obese appropriate for gestational age (AGA) born and non-obese small for gestational age (SGA) born prepubertal Slovak children.
Zuzana Blusková, Ludmila Koštálová, Peter Celec, Eva Vitáriušová, Zuzana Pribilincová

J Pediatr Endocrinol Metab· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Thirty-nine novel neurofibromatosis 1 (NF1) gene mutations identified in Slovak patients.
Martina Nemethova, Anna Bolcekova, Denisa Ilencikova, Darina Durovcikova, Katarina Hlinkova, Anna Hlavata

Ann Hum Genet· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Elevated immunoglobulin D levels in children with PFAPA syndrome.
Laszlo Kovacs, Anna Hlavatá, Marián Baldovič, Ema Paulovicova, Tomas Dallos

Neuro Endocrinol Lett· March 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Food intake, leisure time activities and the prevalence of obesity in schoolchildren in Slovakia.
Eva Vitáriusová, Katarina Babinská, L'udmila Kost'álová, Jozef Rosinský, Anna Hlavatá

Cent Eur J Public Health· December 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein.
Alzbeta Vazna, Clare Beesley, Linda Berna, Larisa Stolnaja, Helena Myskova, Anna Hlavata

Am J Med Genet A· May 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis