Aurora A. Jurca

1 December Sq
Oradea, BH 410081, Romania

Last Updated: 09/26/2026

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Found 15 publications

Clinical Phenotypic Spectrum and Multisystem Burden in Neurofibromatosis Type 1: A Retrospective Regional Cohort Study.

Clinical Phenotypic Spectrum and Multisystem Burden in Neurofibromatosis Type 1: A Retrospective Regional Cohort Study.

Journal: Biomedicines
Published: July 06, 2026

Epilepsy, Cognitive, and Behavioral Outcomes in Neurocutaneous Syndromes: A Comparative Review of NF1, TSC, and Sturge-Weber Syndrome.

Epilepsy, Cognitive, and Behavioral Outcomes in Neurocutaneous Syndromes: A Comparative Review of NF1, TSC, and Sturge-Weber Syndrome.

Journal: Children (Basel, Switzerland)
Published: May 30, 2026

Reproductive Genetic Carrier Screening in Romania: A Couple-Based Study of Pathogenic Molecular Variants.

Reproductive Genetic Carrier Screening in Romania: A Couple-Based Study of Pathogenic Molecular Variants.

Journal: International journal of molecular sciences
Published: March 17, 2026

Tuberous Sclerosis Complex: A Case Series from a Romanian Genetics Center and a Review of the Literature.

Tuberous Sclerosis Complex: A Case Series from a Romanian Genetics Center and a Review of the Literature.

Journal: Journal of clinical medicine
Published: March 11, 2025

Unveiling the complexity of neurofibromatosis type 1: Innovations in genetic understanding and clinical management. A narrative review.

Unveiling the complexity of neurofibromatosis type 1: Innovations in genetic understanding and clinical management. A narrative review.

Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia
Published: January 03, 2025

Tuberous Sclerosis Complex: New Insights into Pathogenesis and Therapeutic Breakthroughs.

Tuberous Sclerosis Complex: New Insights into Pathogenesis and Therapeutic Breakthroughs.

Journal: Life (Basel, Switzerland)
Published: December 30, 2024

Congenital Myasthenic Syndrome-4C in a Consanguineous Romani Family: Genetic Insights and Clinical Implications.

Congenital Myasthenic Syndrome-4C in a Consanguineous Romani Family: Genetic Insights and Clinical Implications.

Journal: Diagnostics (Basel, Switzerland)
Published: December 20, 2024

Clinical Challenges in Diagnosing Primordial Dwarfism: Insights from a MOPD II Case Study.

Clinical Challenges in Diagnosing Primordial Dwarfism: Insights from a MOPD II Case Study.

Journal: Medicina (Kaunas, Lithuania)
Published: October 22, 2024

Wolfram Syndrome Type I Case Report and Review-Focus on Early Diagnosis and Genetic Variants.

Wolfram Syndrome Type I Case Report and Review-Focus on Early Diagnosis and Genetic Variants.

Journal: Medicina (Kaunas, Lithuania)
Published: June 09, 2024

The Role of Aminopeptidase ERAP1 in Human Pathology-A Review.

The Role of Aminopeptidase ERAP1 in Human Pathology-A Review.

Journal: Current issues in molecular biology
Published: January 23, 2024

A New Frameshift Mutation of PTEN Gene Associated with Cowden Syndrome-Case Report and Brief Review of the Literature.

A New Frameshift Mutation of PTEN Gene Associated with Cowden Syndrome-Case Report and Brief Review of the Literature.

Journal: Genes
Published: August 11, 2023

Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways-Case Report and Literature Review.

Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways-Case Report and Literature Review.

Journal: Genes
Published: December 29, 2022
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Last Updated: 09/26/2026