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JRCPE Articles


Volume 55: Issue 1: 2025

A rare presentation of neurofibromatosis mimicking leprosy

Volume 54: Issue 4: 2024

Hereditary haemochromatosis: A review

Volume 53: Issue 4: 2023

Fahr’s syndrome associated with hypoparathyroidism: A case report

Volume 53: Issue 2: 2023

The take-off of Drosophila research in 1930–1950s Edinburgh

Volume 52: Issue 3: 2022

An unusual presentation of type III late onset multiple-acyl-CoA dehydrogenase deficiency leading to a review of its classification system

Volume 52: Issue 2: 2022

Seeing through the cracks

Volume 51: Issue 3: 2021

A family of three with haemoglobin Cheverly: low oxygen saturation in stable patients

Volume 48: Issue 3: 2018

Haemochromatosis arthropathy – a conundrum of the Celtic curse

Volume 48: Issue 2: 2018

Anterior spinal artery syndrome from type A aortic dissection in a patient with Marfan syndrome due to a novel fibrillin mutation

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  • Maternal Medicine, Paediatrics & Genetics - an overview for the general medic 2022
    Category: EMUs 2021-22
  • Acute Medicine: St Andrew's Day 2023
    Category: Acute Medicine: St Andrew's Day
  • Connective Tissues Diseases - Time for Change?
    Category: Joint Specialty Symposia
  • Molecular genetics and atopic eczema
    Category: Webinars

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