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List of works by Guido Davidzon

Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders

scientific article

Application of Deep Learning to Predict Standardized Uptake Value Ratio and Amyloid Status on 18F-Florbetapir PET Using ADNI Data

scientific article published on 04 June 2020

Association of CSF Biomarkers with Hippocampal-dependent Memory in Preclinical Alzheimer Disease

scientific article published on 06 January 2021

Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: Report of a family

scientific article published on 22 June 2007

Bone Marrow and Tumor Radiomics at 18F-FDG PET/CT: Impact on Outcome Prediction in Non-Small Cell Lung Cancer

scientific article published on 17 September 2019

Bridging the Health Data Divide.

scientific article

ChatGPT in nuclear medicine and radiology: lights and shadows in the AI bionetwork

scientific article published in 2023

Deep learning detection of prostate cancer recurrence with 18F-FACBC (fluciclovine, Axumin®) positron emission tomography

scientific article published on 17 June 2020

Early-onset familial parkinsonism due to POLG mutations

scientific article published in May 2006

FDG-PET/CT Initial and Subsequent Therapy Evaluation: Progressing to PET/MR Imaging

scientific article published on 20 August 2012

Mitochondrial DNA and disease

scientific article

NF-κB protein expression associates with (18)F-FDG PET tumor uptake in non-small cell lung cancer: a radiogenomics validation study to understand tumor metabolism

scientific article

Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene

scientific article published on 14 May 2010

POLG mutations and Alpers syndrome

scientific article published on 01 June 2005

Performance Comparison of Individual and Ensemble CNN Models for the Classification of Brain 18F-FDG-PET Scans

scientific article published on 28 October 2019

Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene

article