Albena Jordanova

Sofia, Bulgaria

Last Updated: 09/26/2026

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Found 125 publications

Spectrum of Hereditary Neuropathies in Adult Patients From Serbia.

Spectrum of Hereditary Neuropathies in Adult Patients From Serbia.

Journal: Journal of the peripheral nervous system : JPNS
Published: April 16, 2026

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 24, 2025

Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.

Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.

Journal: Annals of neurology
Published: August 25, 2025

Variant Ataxia-Telangiectasia Presenting as Tremor-Dystonia Syndrome in a Bulgarian Religious Minority.

Variant Ataxia-Telangiectasia Presenting as Tremor-Dystonia Syndrome in a Bulgarian Religious Minority.

Journal: Genes
Published: May 04, 2025

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Journal: Nature communications
Published: March 25, 2025

Molecular Mechanisms of Action of Dendrimers with Antibacterial Activities on Model Lipid Membranes.

Molecular Mechanisms of Action of Dendrimers with Antibacterial Activities on Model Lipid Membranes.

Journal: Polymers
Published: February 17, 2025

Light-driven self-sterilizing cotton fabric and drug delivery: improvement of the antimicrobial activity of 4-sulfo-1,8-naphthalimide via its dendrimer and metallic dendrimer formation.

Light-driven self-sterilizing cotton fabric and drug delivery: improvement of the antimicrobial activity of 4-sulfo-1,8-naphthalimide via its dendrimer and metallic dendrimer formation.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
Published: November 13, 2024

Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.

Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.

Journal: Brain : a journal of neurology
Published: October 27, 2024

Substrate specificity controlled by the exit site of human P4-ATPases, revealed by de novo point mutations in neurological disorders.

Substrate specificity controlled by the exit site of human P4-ATPases, revealed by de novo point mutations in neurological disorders.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 21, 2024

Identification and Characterization of Novel Founder Mutations in NDRG1: Refining the Genetic Landscape of Charcot-Marie-Tooth Disease Type 4D in Bulgaria.

Identification and Characterization of Novel Founder Mutations in NDRG1: Refining the Genetic Landscape of Charcot-Marie-Tooth Disease Type 4D in Bulgaria.

Journal: International journal of molecular sciences
Published: July 18, 2024

Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.

Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.

Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.

Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.

Journal: The Journal of clinical investigation
Published: July 08, 2024
Showing 1-12 of 125

Last Updated: 09/26/2026