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Pide a tu Médico que te haga un test de albumina en orina, fácil, rápido, efectivo para prevenir y proteger tu función renal … are your kidneys OK? #diamundialdelriñon S.E.N. Nefrología Sociedad Madrileña de Nefrología (SOMANE)

la enfermedad renal es silenciosa. si hay antecedentes en tu familia, revisa tus riñones a tiempo! Kidney disease is silent. If you have a family history, get your kidneys checked in time!@SENefrologia #ConcursoDMR25 #worldkidneyday #diamundialdelrinon World Kidney Day ERA - European Renal Association

💚 𝗖𝘂𝗶𝗱𝗮𝗿 𝘁𝘂𝘀 𝗿𝗶ñ𝗼𝗻𝗲𝘀 𝗲𝘀 𝗳𝘂𝗻𝗱𝗮𝗺𝗲𝗻𝘁𝗮𝗹 𝗽𝗮𝗿𝗮 𝗺𝗮𝗻𝘁𝗲𝗻𝗲𝗿 𝘂𝗻𝗮 𝗯𝘂𝗲𝗻𝗮 𝘀𝗮𝗹𝘂𝗱 𝗴𝗲𝗻𝗲𝗿𝗮𝗹 💛 Nuestros riñones desempeñan un papel crucial en mantener nuestro cuerpo funcionando de manera óptima. Las jugadoras de la Academia Voleibol ,

IV jornadas de nefropatías hereditarias del #GTERH S.E.N. Nefrología #adpkd #pqrad #alport #esclerosistuberosa #minoritariasrenales #geneticarenal #rarekidneydiseases 🙌🏻 Sala Llena! 🙌🏻

🙏🏻❤️muchas gracias a todos los que hicieron posible que se realicen las IV jornadas de nefropatías hereditarias 🧬 del #GTERH 🙌🏻 GRACIAS a la secretaria técnica de S.E.N. Nefrología , el pilar fundamental para que todo funcione 🧘🏼 Nos vemos el próximo año! 🧬🥼🩺🩻

ACE estuvo en las IV Jornadas de Nefropatías Hereditarias celebradas en Madrid y organizadas por el grupo #GETRH de S.E.N. Nefrología. ¡Seguimos dando a conocer la #cistinosis para promover el diagnóstico temprano y la atención integral! #nefrologia #EnfermedadesRaras

📢 Vine a la festa del Dia Mundial del Ronyó‼️ Un esdeveniment obert a tothom per conscienciar sobre la importància dels ronyons i la salut renal. 🗓️15 de març, de 10 h a 13:45  🏛️ Recinte Modernista de Sant Pau Informació 👉linke.to/6GTj #DiaMundialdelRonyo

Festa del RONYÓ en Fundació Puigvert Barcelona Sant Pau - Campus Salut Barcelona con las asociaciones de pacientes 🙌🏻👏🏻🙏🏻 Fed. Nac. ALCER oficial AIRG_E Hipofam ACE Asociación Cistinosis España Fabry Support Esclerosis Tuberosa

#April is #FabryDisease Awareness Month 🦓, a great time to raise awareness about this rare genetic disorder that can affect multiple organs, including the kidneys. #Fabry #FabryAwareness #FabryDiseaseAwarenessMonth #raredisease 👇🦓👇🦓👇🦓👇🦓🦓👇 youtu.be/AUkqYvZ9tn0?si…

SGLT2 inhibition for patients with ADPKD – closing the evidence gap 🔓doi.org/10.1093/ndt/gf… This review summarizes the current knowledge on SGLT2i in ADPKD patients & outlines the clinical trial programs in different geographic regions aiming to make SGLT2i accessible

AL Amyloidosis for Cardiologists: Awareness, Diagnosis, and Future Prospects: JACC: CardioOncology State-of-the-Art Review Early diagnosis and correct treatment selection are critical in AL management sciencedirect.com/science/articl…

As we mark this season of hope and renewal, PKD International extends our warmest wishes for Easter to all individuals, families, and partners in the PKD community around the world. #PKDInternational #TogetherForPKD #PKDCommunity #StrongerTogether #ADPKD #ARPKD

La “OMEPRALIZACION” silenciosa de la sociedad está normalizando el uso crónico del omeprazol, fármaco que deberían ser temporales y revisados. Como médico especialistas, tenemos la responsabilidad de revisar y educar: el omeprazol no es un suplemento ni un protector universal.

We are pleased to announce the publication of the KDIGO 2025 Clinical Practice Guideline for the Management of Nephrotic Syndrome in Children. Read the News Release: kdigo.co/NS-in-Children… Read the Guideline in Kidney International: kdigo.co/Nephrotic-Synd… Download the Guideline:

🫘Alport Syndrome Decoded 🧬Missense: Misfolded collagen→ ER stress→ podocyte death Vs 🧬Truncating: No collagen→ weak GBM→ mesangial filopodia invade! ET-1, DDR1, integrins→ fibrosis & inflammation🤕 🔗 doi.org/10.1681/ASN.00… #Nephrology #AlportSyndrome #MedTwitter

👩‍⚕️ Patricia has been actively conducting research into #ADPKD and #ARPKD as Professor of Medicine for over 20 years. Knowledge gained about the mechanisms of how #PKD kidneys enlarge and develop cysts has led to new ways to develop therapies. #PKDInternational

Novartis has agreed to acquire Regulus Therapeutics, a clinical-stage biopharmaceutical company focused on developing microRNA therapeutics with a focus on autosomal dominant polycystic kidney disease (ADPKD), a severe renal disease. For more information and cautionary

💛 Every donation brings us closer to a world without #PKD. Polycystic Kidney Disease affects millions of people globally — but together, we can change lives. 👉 Donate today and be part of the change: 🔗 pkdinternational.org/donate #ADPKD #ARPKD #PKDAwareness #PatientSupport

🧬Here a brief and highly appropriate summary of pregnancy management in women with #ADPKD #GTERH Societat Catalana de Nefrologia S.E.N. Nefrología JovSEN

#PKDKnowledge Series - Ep. 2, Flavia Galletti shares a clear message: 🗣️ “#OpenScience is sharing knowledge to build a more inclusive picture and reach better results, faster.” 🇪🇺 The #OSCARSproject is piloting a new way of working #ADPKD #CollaborationInScience #PatientAdvocacy