Mariela S. Militaru
Bucharest, B 020027, Romania
Last Updated: 09/26/2026
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Found 30 publications
Functional Germline DNA Repair Mutations as Predictors of Acute Radiodermatitis in Breast Cancer.
Journal: Diagnostics (Basel, Switzerland)
Published: January 29, 2026
Prenatal Diagnosis of Sex Chromosome Aneuploidies: A Retrospective Study Using QF-PCR, SNP-Based Chromosomal Microarray Analysis, and NIPT.
Journal: Genes
Published: January 19, 2026
Oxidative stress and immunomarkers in equine dermal melanomatosis: single-case comparison with healthy individual.
Journal: Journal of equine veterinary science
Published: January 10, 2026
Emotional distress and quality of life in high and moderate penetrance germline mutations carriers diagnosed with breast cancer: a preliminary study.
Journal: Medicine and pharmacy reports
Published: May 26, 2025
Associations Between DNA Repair Gene Polymorphisms and Breast Cancer Histopathological Subtypes: A Preliminary Study.
Journal: Journal of clinical medicine
Published: May 04, 2025
The Impact of Genetic Variations on Radiotherapy Toxicity in Breast Cancer Patients: A Meta-Analysis of Acute and Late Skin Adverse Effects.
Journal: Cancers
Published: April 19, 2025
Quality-of-Life Assessment in Patients Undergoing Mastectomy and Breast Reconstruction for Moderate-Penetrance Gene-Related Breast Cancer.
Journal: Journal of clinical medicine
Published: January 26, 2025
The Impact of Chromosomal Mosaicisms on Prenatal Diagnosis and Genetic Counseling-A Narrative Review.
Journal: Journal of personalized medicine
Published: June 14, 2024
Primary ciliary dyskinesia: a case report of double DNAH11 mutant alleles.
Journal: Medicine and pharmacy reports
Published: May 06, 2024
Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review.
Journal: Medicina (Kaunas, Lithuania)
Published: April 11, 2024
Breast Cancer Screening and Prophylactic Mastectomy for High-Risk Women in Romania.
Journal: Medicina (Kaunas, Lithuania)
Published: February 12, 2024
Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array.
Journal: Journal of personalized medicine
Published: January 26, 2024
Last Updated: 09/26/2026