An aspiring researcher is encouraging other health and care professionals to be part of a NIHR development programme which has inspired her to become a Principal Investigator.
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Latest research led from Manchester could revolutionise the diagnosis of Perrault syndrome, a rare genetic condition that results in hearing loss.
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An international team of scientists are to set to use thousands of MRI brain scans from research teams around the world in a bid to study NF1, a lifelong neurological condition.
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In the largest study of its kind, UK clinicians and researchers at RMCH and GOSH have jointly developed a highly innovative, life-changing surgery for children with a rare genetic condition.
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The Pharmacogenetics Roll Out – Gauging Response to Service [PROGRESS] programme is an NHS England funded transformation project led by researchers at Manchester University NHS Foundation Trust.
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Greater Manchester residents are being encouraged to take part in a research study at MREH that aims to improve the diagnosis and treatment of conditions associated with sight loss.
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A ground-breaking genetic test that could prevent critically ill newborn babies going deaf if treated with a commonly used antibiotic, is being trialled across 14 NHS neonatal units.
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Researchers have shown that their system, developed at MFT, can identify more breast cancer patients who are eligible for testing for inherited faulty genes that can cause breast cancer.
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