Very good reception at the presentation of PATIENT73 during the World Orphan Drug Congress
The presentation served to show the current status of the platform and its strengths, as well as the next steps to be taken in the future.
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The presentation served to show the current status of the platform and its strengths, as well as the next steps to be taken in the future.
The 13th edition of the World Orphan Drug Congress, an award-winning event that has become the world's largest meeting on orphan drugs and rare diseases, will take place at the Hotel Melià Sitges (Barcelona) from November 14 to 17.
Next Friday, November 11 at 19:30h we will present online the Patient73Hub project.
Agenda Patient73 |
The event, focused on the current situation of research on rare diseases in Spain, will take place on November 4 from 10 a.m. to 12:30 p.m. at Unidad Editorial's headquarters in Madrid.
The PATIENT73 team attends the 8th edition of the reference congress on Artificial Intelligence and Big Data: the
AI & Big Data Congress.
El proper 26 d'octubre es celebren les XXXIV Jornades Tècniques ESTIMULACIÓ CEREBRAL NO INVASIVA;´LHORA DE LA CLÍNICA a l'Institut de Salut Cerebral i Neurorehabilitació Guttmann Barcelona. Inscripcions a partir del 23 de setembre.
Assistim al Congrés sobre el canvi de model assistencial que es celebra el 28 i 29 de setembre a Barcelona.
On Wednesday 21st of December 2022, we invite you to participate in the training conference for Idiopathic Pulmonary Fibrosis (IPF) aimed at healthcare workers, especially pulmonologists and workers at primary care centres (CAP in Catalan) and primary care emergency centres (CUAP in Catalan).
El proper dissabte 24 de setembre a les 11:00h se celebra el Dia Internacional de la Hipercolesterolèmia Familiar a l'auditori de l'Hospital Universitari Sant Joan (Reus)
Researchers are trying to pinpoint if TRAF7 patients have an increased risk of certain cancers such as meningiomas, mesotheliomas, intraneural perineurinomas or adenomatoid tumours of the genital tract.
You can now sign up for the First Conference for Hereditary Connective Tissue Disorders, organised by @conectiva_lat and @mundomarfan with the collaboration of @CentroCREER in Burgos, Spain, from the 27th to the 30th of September.
The event takes inspiration from the title of Michel Foucault’s work The Order of Things: An Archaeology of the Human Sciences (Words and Things: An Archaeology of the Human Sciences in French) and will focus on the word that “separates” us from the rest of the population.
Photography exhibitioin "Malalties Minoritàries" travels to Castellbisbal from the 8th to the 30th of June, 2022.
Rare and undiagnosed diseases are usually pathologies that, individually, affect a not very large number of people, but as a whole the "thing" changes.
The next 2 to 5 May will be held at the WTC in Barcelona the XXVI annual meeting of the Catalan society of neurology.
ERKNet, the European Reference Network for Rare Kidney Diseases, wants to offer the exceptional expertise of its internationally renowned specialists to European patients affected by rare kidney diseases and their families.
This Sunday, April 24 at 12:30 pm at SILK La moraleja, a new charity party “Helping is fun”.
This activity is part of the cycle on double discrimination. Approximation to this theme from ethics, philosophy, psychology, and sociology.
Share your experience in finding a diagnosis for your rare disease
On Thursday, 31 March, the 2nd Community Day of Mental Health and Work will be held in the district of Sant Andreu: "Sharing experiences around the care", organized by the Taula de Salut Mental de Sant Andreu.
