We are the combination of four hospitals: the General Hospital, the Children’s Hospital, the Women’s Hospital and the Traumatology, Rehabilitation and Burns Hospital. We are part of the Vall d’Hebron Barcelona Hospital Campus: a world-leading health park where healthcare plays a crucial role.
Patients are the centre and the core of our system. We are professionals committed to quality care and our organizational structure breaks down the traditional boundaries between departments and professional groups, with an exclusive model of knowledge areas.
Would you like to know what your stay at Vall d'Hebron will be like? Here you will find all the information.
The commitment of Vall d'Hebron University Hospital to innovation allows us to be at the forefront of medicine, providing first class care adapted to the changing needs of each patient.
Miguel Molina Berenguer, Investigador del Grup de Recerca en Patologia Neuromuscular i Mitocondrial
L'hepatoencefalopatia deguda a la deficiència de fosforilació oxidativa combinada tipus 1 (COXPD1) és un trastorn de la traducció mitocondrial recessiu causat per mutacions en GFM1, un gen nuclear que codifica el factor d'allargament mitocondrial G1 (EFG1). Els pacients amb COXPD1 solen presentar hepatoencefalopatia aviat després del naixement amb una progressió ràpida de la malaltia i solen morir durant les primeres setmanes o anys de vida.
Amfitrió: Dr. Ramón Martí Seves, Cap del grup de Patologia Neuromuscular i Mitocondrial
Format: Accés gratuït i presencial.
En línia: https://gencat.zoom.us/j/94088176658
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