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Touch in infancy is important for healthy brain development

23 March 2017

Research

NDCN honorary consultant wins award for research into inherited retinal disease

15 December 2014

Awards and Appointments

On 3 December the Oxford University Hospitals Staff Recognition Awards took place at the Oxford Museum of Natural History. These awards marked the outstanding achievements, hard work and dedication shown by hospital staff.

Metal-on-metal revision research takes centre-stage at world’s largest orthopaedic conference

16 March 2017

Research

A new study on patient outcomes after metal-on-metal hip replacement revision surgery has been selected as part of a prestigious 'Game Changers' session at the American Academy of Orthopaedic Surgeons (AAOS) annual meeting.

Farewell message from the outgoing Head of Division, Professor Alastair Buchan

16 January 2017

10,000th patient for pioneering cardiac genetic testing service

23 September 2016

Research

The largest NHS-based centre to identify genetic causes of heart disease has welcomed its 10,000th patient. Founded by Oxford University and NHS staff, the Oxford Medical Genetics Laboratory at the Churchill Hospital began its cardiac genetic testing service in 2003 and was the first accredited NHS diagnostic genetic testing service for inherited cardiac conditions (ICC) in the UK.

European Researchers' Night 2017: Update

14 November 2016

Highlights from the Medical Sciences Board Meetings

13 February 2017

Bending the blood pressure curve down: are we succeeding?

18 November 2016

Until just a few decades ago, raised blood pressure was regarded as a benign and natural process of ageing that did not warrant treatment.

New guide for parents who are coping with their child's self-harm: 'You are not alone'

1 December 2015

General Research

Senior Fellow in Image Analysis of Growth and Development joins NDOG

18 August 2015

Awards and Appointments General

The Nuffield Department of Obstetrics & Gynaecology (NDOG) is pleased to announce that Professor Peter Hammond, a world leader in the analysis of facial dysmorphism in rare genetic syndromes, has joined the department.