Transplantační medicína

Citation: Geba et al. Journal of Allergy and Clinical Immunology 2025;Vol.151: 756-766

Citation: Geba et al. Journal of Allergy and Clinical Immunology 2025;Vol.151: 756-766

Σε αυτό το σύντομο βίντεο η Dr. Cheng επισημαίνει ότι τα δεδομένα για την ινσουλίνη Glargine 300 (Toujeo^®) καλύπτουν ένα ευρύ φάσμα ασθενών με διαφορετικά χαρακτηριστικά.

Εκπαιδευτική παρουσίαση που εξετάζει τον κρίσιμο ρόλο των Αποτελεσμάτων που Αναφέρονται από τους Ασθενείς (Patient-Reported Outcomes - PROs) στη διαχείριση του Σακχαρώδη Διαβήτη τύπου 2

Az Egészségügyi Világszervezet (WHO) szerint az elmúlt években a túlsúly és annak elhízássá alakulása komoly globális közegészségügyi problémává vált, amely milliókat érint, és hatalmas negatív hatással van a népesség egészségére¹.

Rare Disease Day raises awareness for the 300 million people worldwide living with a rare disease, along with their families and carers. Over 6,000 rare diseases are characterized by a wide range of conditions and symptoms that can vary not only between diseases but also among individuals with the same condition. Take the opportunity to support equitable access to diagnosis, treatment, healthcare, social support for those affected by rare diseases.

Rare Disease Day raises awareness for the 300 million people worldwide living with a rare disease, along with their families and carers. Over 6,000 rare diseases are characterized by a wide range of conditions and symptoms that can vary not only between diseases but also among individuals with the same condition. Take the opportunity to support equitable access to diagnosis, treatment, healthcare, social support for those affected by rare diseases.

Rare Disease Day raises awareness for the 300 million people worldwide living with a rare disease, along with their families and carers. Over 6,000 rare diseases are characterized by a wide range of conditions and symptoms that can vary not only between diseases but also among individuals with the same condition. Take the opportunity to support equitable access to diagnosis, treatment, healthcare, social support for those affected by rare diseases.