
Manchester research leads to NHS roll out of life-saving treatment for babies with rare disease
Babies and toddlers with a rare and fatal genetic condition can now receive life-saving treatment on the NHS for the first time.
Read moreBabies and toddlers with a rare and fatal genetic condition can now receive life-saving treatment on the NHS for the first time.
Read moreFor World Antimicrobial Awareness Week, Dr Jan Hansel discusses the importance of therapeutic drug monitoring (TDM) in limiting the development of antimicrobial resistance and the new TDM-TIME study.
Read moreThe Department of Health and Social Care has announced that a new NIHR Research Delivery Network will commence in 2024 to support the successful delivery of health and social care research in England.
Read moreNIHR has awarded MFT £2,998,433 from 1 April 2024 to develop innovative technology solutions for better diagnosis, treatment, and care for people across our region.
Read moreIn the latest Spotlight On blog, Dr Ahmed discusses the breakthrough STEP HFpEF study and the importance of equality, diversity and inclusivity in research, sharing her first-hand experiences of this.
Read moreThe UK regulatory authorities have approved the first ever trial of a revolutionary gene therapy for young children diagnosed with Hunter syndrome, a devastating rare lysosomal storage disorder.
Read moreITV Tyne Tees and Granada Reports recently featured the journey of two-year-old Teddi Shaw, who became the first child in the UK to receive NHS life-saving gene therapy treatment, Libmeldy® at MFT.
Read moreR&I colleagues welcomed James McLaughlin, Chief Executive for Cure Leukaemia, to MFT, as he ran 14 km across Manchester to raise funds for blood cancer research at Manchester Royal Infirmary (MRI).
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