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Dr Wendy Heywood

Dr Wendy Heywood awarded investigator initiated research proposal from Shire Pharmaceuticals

28 Jun 2016, 2:01 p.m.

Following NIHR Great Ormond Street BRC support, which led to the creation of a high-throughput targeted proteomic urine test, Dr Wendy Heywood has been awarded an industry investigator initiated award from Shire Pharmaceuticals.

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medical devices workshop

Driving forward medical device development

2 Oct 2019, 4:57 p.m.

The NIHR GOSH BRC last month hosted an inaugural medical devices workshop, in partnership with the UCL Institute of Healthcare Engineering.

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​Drug for Duchenne Muscular Dystrophy shows promise in clinical trial

21 Aug 2017, 12:02 p.m.

An international clinical trial has found that the drug ataluren can improve mobility for children with a severe form of Duchenne muscular dystrophy (DMD).

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The Dubowitz Neuromuscular Centre at GOSH and the ICH is a Muscular Dystrophy UK Paediatric Centre for Research and Clinical Excellence

Dubowitz Neuromuscular Centre confirmed as Centre of Paediatric Clinical and Research Excellence

22 Mar 2016, 3:37 p.m.

The Dubowitz Neuromuscular Centre has been confirmed as a Centre of Paediatric Clinical and Research Excellence by Muscular Dystrophy UK.

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Film celebrates success of Biomedical Research Centres set up by outgoing UK Chief Medical Officer

14 Oct 2019, 11:37 a.m.

NHS patients who have taken part in clinical trials have expressed their gratitude to researchers in a film celebrating the work of the National Institute for Health Research (NIHR) Biomedical Research Centres (BRCs), including GOSH BRC, to mark the retir

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First children have gene therapy treatment for blindness at GOSH

18 Feb 2020, 5:33 p.m.

The first paediatric patients have received a pioneering new gene therapy that can restore eyesight at Great Ormond Street Hospital.

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Phoebe and Fenella took part in a clinical trial at GOSH

First drug to reduce fever flares in children with recurrent fever conditions

17 Aug 2018, 12:02 p.m.

Injections of the drug canakinumab significantly reduced the number of fever episodes in children with three different types of recurrent fever conditions, in an international trial led at GOSH by Professor Paul Brogan.

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Test tubes on a revolving plate in a lab

Funding boost to develop novel therapy for rare metabolic condition

1 Apr 2019, 10:19 a.m.

GOSH and UCL Great Ormond Street Institute of Child Health (ICH) researchers Professor Paul Gissen and Dr Julien Baruteau will be part of a new collaboration with Evox Therapeutics that aims to develop a new therapy for the life threatening metabolic cond

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Funding to develop immunotherapy for childhood sarcomas

18 Dec 2015, 1:01 p.m.

Biomedical Research Centre (BRC) supported Professor John Anderson has been awarded funding from Children with Cancer UK to investigate new immunotherapy approaches for childhood sarcomas.

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Funding provided to develop new therapy for acute liver failure

9 Sep 2015, 4:50 p.m.

BRC-supported researcher Dr Kevin Mills has been awarded funding from the NIHR to investigate the regenerative ability of the liver following acute liver failure (ALF). If successful, the team hope that their research will lead to a novel therapy that cou

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Funding success for Parkinson’s research

24 Sep 2020, 1 p.m.

Two multi-million-pound research grants will fund a pioneering new programme of research aimed at understanding and tackling Parkinson’s disease, including vital genetic investigations at the UCL Great Ormond Street Institute of Child Health (ICH).

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Sterile GOSgene laboratory

Gene therapy treatment manufactured at GOSH and ICH used to treat world's first patient with life limiting genetic condition, MPSIIIA

28 May 2019, noon

A two-year old patient at the Royal Manchester Children’s Hospital (RMCH) is the first in the world to receive a pioneering new gene therapy treatment for the rare and life-limiting genetic condition, Mucopolysaccharidosis IIIA (MPSIIIA). The treatment wa

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Dr Claire Booth

Gene therapy trial for patients with Fanconi anaemia to open at GOSH

22 Mar 2016, 5:24 p.m.

A clinical trial is to open at Great Ormond Street Hospital (GOSH) that will test the use of gene therapy during transplantation for the treatment of young people with Fanconi anaemia.

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Trying a vegetable biopsy at the BRC Family Fun Day

Getting hands-on with research

23 Oct 2018, 2:58 p.m.

Last weekend, we opened our doors to over 300 visitors for the annual Family Fun Day hosted by the National Institute for Health Research (NIHR) Great Ormond Street Hospital (GOSH) Biomedical Research Centre (BRC).

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GOSH awarded £37 million funding to carry out pioneering paediatric research

14 Sep 2016, 5:39 p.m.

The NIHR Great Ormond Street Biomedical Research Centre (BRC) has been awarded £37 million in funding to drive forward translational research into rare diseases in children. The Centre is the only one of its kind in the UK dedicated to paediatric research

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GOSH BRC researchers receive NIHR Senior Investigator awards

4 Apr 2016, 12:45 p.m.

Professors Francesco Muntoni, Jane Sowden and Helen Cross who have all been successfully appointed as new NIHR Senior Investigators.

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GOSH research brings Duchenne muscular dystrophy drug one step closer to UK patients

5 Mar 2020, 9:30 p.m.

A drug that ‘skips over’ a genetic fault responsible for the fatal muscle-wasting condition Duchenne muscular dystrophy (DMD) has shown promising results in an international trial led by Great Ormond Street Hospital (GOSH).

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GOSH researchers receive UCL Business Award

23 Jun 2017, 12:57 p.m.

Professors Bobby Gasper and Adrian Thrasher, both members of the BRC senior management team, have been awarded the UCL Business Award, in recognition of their work on the spin-out company Orchard Therapeutics.

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GOSH set to take part in world first human challenge study to find a COVID-19 vaccine

27 Oct 2020, 11:02 a.m.

National Institute of Health Research (NIHR) Great Ormond Street Hospital Biomedical Research Centre is set to play a crucial role in a new study exploring the possibility of running the first human challenge study to find a vaccine for COVID-19.

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High throughput screening identifies the genetic cause underlying a rare disease in a large nationwide cohort

18 Dec 2015, 1:20 p.m.

A collaborative study between ICH and the Turkish Pediatric Endocrinology Society has used high throughput DNA analysis to identify the genetic cause of primary adrenal insufficiency in more than 80% of affected children.

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