This study is the result of a multidisciplinary approach and focuses on a case of considerable historical and medical interest. The work originally stemmed from findings at a funerary site in the area of Casal Bertone in Rome (Italy), regards an individual in a tomb identified simply by the number “75.” The skeletal alterations that were later discovered gave rise a debate among the members of the team. Challenges in identifying the pathology have brought historians, anthropologists, and radiologists into the field with the use of sophisticated equipment, including CT scans and X‐ray equipment, as well as some analyses carried out with the latest spectrometers. Consequently, the most likely diagnostic hypothesis resulted in gout. During thi...
OBJECTIVE. According to the written sources several members of the famous Medici family of Renaissan...
We present a case of cauterisation observed in a skull of an adult female from 8-10th century Pisa
Distal renal tubular acidosis is a rare genetic disease, characterised by deficit in renal tubular t...
This study is the result of a multidisciplinary approach and focuses on a case of considerable histo...
The study of pathological alterations in ancient skeletal remains may contribute to the reconstructi...
This study is the result of a multidisciplinary team approach and focuses on a case of considerable ...
The article examines the truthfulness of historical accounts claiming that the Renaissance Duke Fede...
The article examines the truthfulness of historical accounts claiming that Renaissance Duke Federico...
OBJECTIVES: Throughout history, gout has been referred to as the "disease of the kings", and has ...
Acknowledgements The authors would like to thank Trish Biers of the Duckworth Collection at the Univ...
This book presents the results of a unique macroscopic and radiological analysis, by X-ray and CT sc...
Objectives: This study was conducted to test several hypotheses: 1. That rheumatoid arthritis and sy...
Background: Few diseases that confront the 21st century clinician have documented history which date...
Gout is a medical condition with typical recurrent attacks of acute inflammatory arthritis. The seve...
Frederick of Montefeltro (1422-1482), Duke of Urbino, is one of the foremost warlords and patron of ...
OBJECTIVE. According to the written sources several members of the famous Medici family of Renaissan...
We present a case of cauterisation observed in a skull of an adult female from 8-10th century Pisa
Distal renal tubular acidosis is a rare genetic disease, characterised by deficit in renal tubular t...
This study is the result of a multidisciplinary approach and focuses on a case of considerable histo...
The study of pathological alterations in ancient skeletal remains may contribute to the reconstructi...
This study is the result of a multidisciplinary team approach and focuses on a case of considerable ...
The article examines the truthfulness of historical accounts claiming that the Renaissance Duke Fede...
The article examines the truthfulness of historical accounts claiming that Renaissance Duke Federico...
OBJECTIVES: Throughout history, gout has been referred to as the "disease of the kings", and has ...
Acknowledgements The authors would like to thank Trish Biers of the Duckworth Collection at the Univ...
This book presents the results of a unique macroscopic and radiological analysis, by X-ray and CT sc...
Objectives: This study was conducted to test several hypotheses: 1. That rheumatoid arthritis and sy...
Background: Few diseases that confront the 21st century clinician have documented history which date...
Gout is a medical condition with typical recurrent attacks of acute inflammatory arthritis. The seve...
Frederick of Montefeltro (1422-1482), Duke of Urbino, is one of the foremost warlords and patron of ...
OBJECTIVE. According to the written sources several members of the famous Medici family of Renaissan...
We present a case of cauterisation observed in a skull of an adult female from 8-10th century Pisa
Distal renal tubular acidosis is a rare genetic disease, characterised by deficit in renal tubular t...