Publications by authors named "Atasie Diter"

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Familial Von Hippel-Lindau Disease: A Case Series of Cerebral Hemangioblastomas with MRI, Histopathological, and Genetic Correlations.
Claudiu Matei, Ioana Boeras, Dan Orga Dumitriu, Cosmin Mutu, Adriana Popescu, Diter Atasie

Life (Basel)· October 2025

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Understanding Burnout in Forensic Medicine and the Interaction of Job Satisfaction and Unconditional Self-Acceptance: A Cross-Sectional Study.
Lilioara-Alexandra Oprinca-Muja, Adrian-Nicolae Cristian, Elena Topîrcean, Alina Cristian, Marius Florentin Popa, Diter Atasie

Healthcare (Basel)· May 2025

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Exploring Burnout at the Morgue During the COVID-19 Pandemic: A Three-Phase Analysis of Forensic and Pathology Personnel.
Lilioara-Alexandra Oprinca-Muja, Adrian-Nicolae Cristian, Elena Topîrcean, Alina Cristian, Marius Florentin Popa, Diter Atasie

Healthcare (Basel)· February 2025

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Lack of Association Between BsmI and FokI Polymorphisms of the VDR Gene and Sporadic Colorectal Cancer in a Romanian Cohort-A Preliminary Study.
Bianca Petre-Mandache, Emilia Burada, Mihai Gabriel Cucu, Diter Atasie, Anca-Lelia Riza

Curr Oncol· October 2024

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Exploring Therapeutic Challenges in Patients with HER2-Positive Breast Cancer-A Single-Center Experience.
Ramona Coca, Andrei Moisin, Rafaela Coca, Atasie Diter, Mihaela Racheriu

Life (Basel)· August 2024

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Wolfram Syndrome Type I Case Report and Review-Focus on Early Diagnosis and Genetic Variants.
Alexandru Daniel Jurca, Larisa Bianca Galea-Holhos, Aurora Alexandra Jurca, Diter Atasie, Codruta Diana Petchesi

Medicina (Kaunas)· June 2024

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Detection of SARS-CoV-2 Viral Genome and Viral Nucleocapsid in Various Organs and Systems.
George Călin Oprinca, Cosmin-Ioan Mohor, Alina-Simona Bereanu, Lilioara-Alexandra Oprinca-Muja, Iancu Bogdan-Duică, Atasie Diter

Int J Mol Sci· May 2024

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Unveiling the Pathological Mechanisms of Death Induced by SARS-CoV-2 Viral Pneumonia.
George-Călin Oprinca, Cosmin-Ioan Mohor, Alexandra Oprinca-Muja, Adrian Hașegan, Adrian-Nicolae Cristian, Diter Atasie

Microorganisms· February 2024

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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.
Cristina Gug, Lavinia Caba, Ioana Mozos, Dana Stoian, Diter Atasie

Gene· May 2020

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