Miruna Gug

Eftimie Murgu Square 2
Timisoara, TM 300041, Romania

Last Updated: 09/26/2026

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Found 8 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

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

The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular Variants.

The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular Variants.

Journal: International journal of molecular sciences

Published: October 10, 2025

The Role of Age and Comorbidity Interactions in COVID-19 Mortality: Insights from Cardiac and Pulmonary Conditions.

The Role of Age and Comorbidity Interactions in COVID-19 Mortality: Insights from Cardiac and Pulmonary Conditions.

Journal: Journal of clinical medicine

Published: November 14, 2024

Impact of Vaccination Status on COVID-19 Severity and Pulmonary Involvement.

Impact of Vaccination Status on COVID-19 Severity and Pulmonary Involvement.

Journal: Medicina (Kaunas, Lithuania)

Published: October 12, 2024

Approach and Management of Pregnancies with Risk Identified by Non-Invasive Prenatal Testing.

Approach and Management of Pregnancies with Risk Identified by Non-Invasive Prenatal Testing.

Journal: Journal of personalized medicine

Published: February 15, 2024

Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population.

Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population.

Journal: Medicina (Kaunas, Lithuania)

Published: November 27, 2021

Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literature.

Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literature.

Journal: Gene

Published: November 20, 2019

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Last Updated: 09/26/2026