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Artikel
Reflekter over ny tilgang til KOL
At få en forståelse for type 2 inflammation* kan belyse hvorfor nogle KOL-patienter fortsætter med at få eksacerbationer.1
FLUNITY-HD : the largest individually randomised influenza vaccine effectiveness study of its kind.
FLUNITY-HD is the largest individually randomised influenza vaccine effectiveness study, with nearly half a million older adults across multiple seasons.1
Defining ITP
Low platelet counts are one facet of ITP, but when we look at it from another angle, we see the multiple dimensions of ITP. ITP is a condition of complex immune dysregulation that reduces platelet counts—causing bleeding, bruising, fatigue, and other health-related quality-of-life (HRQoL) issues—while increasing inflammation and the risk of thromboembolic events (TEs).1-5
Living with ITP
Patients reported significant quality of life (QoL) challenges related to their ITP1
Assessing fatigue in ITP patients
For ITP patients, several scales are available to measure and track fatigue and its impact on quality of life. These tools can help patients and healthcare providers gauge symptoms and adjust their ITP treatment accordingly.1-4
Mechanism of Disease
Complex immune dysregulation can lead to autoimmunity and inflammation1-6
Uddannelse
INTERVIEW: Kliniske erfaringer fra Tyskland
I Tyskland har adgang til biologisk behandling til den ukontrollerede KOL patient, været mulig i et år. (12/2025)
FLUNITY-HD: Results of the pooled analysis of the two individually randomized real-world studies, DANFLU 2 and GALFLU
Monday September 15th, 2025 16:00-17:15 CET
A heart for Fabry - Podcast
A podcast series designed by cardiologists, for cardiologists and other healthcare professionals.
Polyp Gossip - latest episode
Polyp Gossip is a video podcast dedicated to exploring Chronic Rhinosinusitis with Nasal Polyps (CRSwNP). Hosted by two globally recognized rhinologists. The show delves into trending topics, latest advancements, and patient experiences. Each episode features esteemed guests, including experts and patients, offering valuable insights into the evolving world of CRSwNP.
Podcasts
Polyp Gossip
Polyp Gossip is a video podcast dedicated to exploring Chronic Rhinosinusitis with Nasal Polyps (CRSwNP). Hosted by two globally recognized rhinologists. The show delves into trending topics, latest advancements, and patient experiences.
The Hematology Podcast
Welcome to The Hematology Podcast, your source for the latest insights into hematology and rare blood disorders. This podcast covers cutting-edge research, clinical advancements, and real-world cases tailored for healthcare professionals.
A heart for Fabry - Podcast
A podcast series designed by cardiologists, for cardiologists and other healthcare professionals.
Hot topics in atopic dermatitis
This podcast episode highlights an engaging discussion on managing atopic dermatitis, featuring Dr. Andrew Pink, a consultant dermatologist from UK. Emmanuel Tony and Ashlyn Kerry guide the conversation. Dr. Pink discusses the challenges and strategies in treating eczema, emphasizing personalized treatment plans and the importance of patient communication.
RespTalks
Resptalks er en række af videnskabelige webinars og podcasts inden for emner som relaterer til det respiratoriske sygdomme som som astma, kronisk rhinosinuitis med næsepolypper til type 2 inflammation og meget andet. Indholdet er målrettet lungelæger, øre-næse-halslæger, allergologer, børnelæger, forskere fra de nordiske- og BeNeLux landene.
Treatable Traits & Asthma
En podcast om "treatable traits" ved astma med professor Backer, Pavord og Gibson. Denne podcast er for sundhedspersonale, der er interesseret i at lære mere om, hvordan man behandler astmapatienter på den mest optimale måde i henhold til tilgængelig videnskab og kliniske erfaringer.
Podcast om Min Sjældne Sygdom
I podcastserien ”Min Sjældne Sygdom” inviterer vært Bo Rafn, Medicinsk Rådgiver fra Sanofi, en af Danmarks førende specialister i studiet for at tale om et sjældent sygdomsområde. Sammen med eksperten i hver episode giver de lytteren en unik mulighed for at få indblik i symptomer, diagnose og hvordan man som patient, skal leve med en sjælden sygdom.