Kristel Klaassen
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 29 publications
RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3.
Journal: Diseases (Basel, Switzerland)
Published: April 27, 2026
Behçet's syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case report.
Journal: Frontiers in immunology
Published: February 03, 2026
First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review.
Journal: Diseases (Basel, Switzerland)
Published: January 09, 2026
Multiphasic acute disseminated encephalomyelitis (MDEM) in a patient with systemic lupus erythematosus and C4A deficiency: case-based review.
Journal: Rheumatology international
Published: June 26, 2025
Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant.
Journal: Scientific reports
Published: February 17, 2025
Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity.
Journal: International journal of molecular sciences
Published: July 30, 2024
Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies.
Journal: Molecular diagnosis & therapy
Published: May 26, 2024
Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemia.
Journal: Frontiers in immunology
Published: October 19, 2023
The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis.
Journal: International journal of molecular sciences
Published: May 25, 2023
Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases.
Journal: Life (Basel, Switzerland)
Published: July 16, 2022
Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier.
Journal: Molecular genetics and metabolism reports
Published: August 23, 2021
Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity.
Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity.
Journal: Frontiers in nutrition
Published: March 31, 2021
Last Updated: 09/26/2026