Anna Cechova
Prague, PR, Czech Republic
Last Updated: 09/26/2026
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Found 13 publications
Transcranial direct current stimulation in affecting neuropsychiatric symptoms of post-COVID syndrome: No change in microstates and functional connectivity.
Journal: PloS one
Published: October 23, 2025
Glycogen storage disease type IX: Long-term follow-up of 52 patients from three European countries.
Journal: Molecular genetics and metabolism reports
Published: October 09, 2025
Transcranial direct current stimulation and cognitive training in the treatment of cognitive deficit in schizophrenia: a randomized controlled trial.
Journal: BMC psychiatry
Published: August 31, 2025
Genotype/Phenotype Relationship: Lessons From 137 Patients With PMM2-CDG.
Journal: Human mutation
Published: November 30, 2023
Physical Activity and BMI before and after the Situation Caused by COVID-19 in Upper Primary School Pupils in the Czech Republic.
Journal: International journal of environmental research and public health
Published: November 28, 2021
Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency?
Journal: Molecular genetics and metabolism
Published: April 08, 2021
ALG3-CDG: a patient with novel variants and review of the genetic and ophthalmic findings.
Journal: BMC ophthalmology
Published: March 03, 2021
Congenital disorders of glycosylation: Still "hot" in 2020.
Journal: Biochimica et biophysica acta. General subjects
Published: June 29, 2020
International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): Diagnosis, follow-up, and management.
Journal: Journal of inherited metabolic disease
Published: April 20, 2020
Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation.
Journal: Journal of inherited metabolic disease
Published: February 07, 2020
Attenuated Type of Asphyxiating Thoracic Dysplasia due to Mutations in DYNC2H1 Gene.
Journal: Prague medical report
Published: January 15, 2020
Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case.
Journal: Folia biologica
Published: October 23, 2019
Last Updated: 09/26/2026