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trasplantation

Homepage trasplantation

FEDERG at the 47th Congress of the Spanish Association of Nephrology in Bilbao 2024

CKD, Congress, kidney diseases, trasplantation
Conferences, Health, Meetings

Mireya Carratalá, Antonio Cabrera and Susana Carvajal, representing FEDERG, Alcer, Hipofam, Ahua and AIRG Spain, participated in the Congress. The…

1 August 2024
0
717

f2f FEDERG Metting, Fighting for our Federation, 10 years, 2024.

CKD, ERN-Erknet, EURORDIS, kidney diseases, Rare Disease, trasplantation
Education, Health, Meetings

FEDERG, moving forward and fighting for rare and genetic kidney diseases

1 August 2024
0
762

FEDERG at the 47th Congress of the AENP Spanish Association of Pediatric Nephrology, May 2024.

Education, Rare Disease
CKD, kidney diseases, Rare Disease, trasplantation

Susana Carvajal Arjona (FEDERG, hipofam) Mireya Carratalá (FEDERG ASHUA)

25 May 2024
0
2124

About Us

FEDERG is the non-profit federation of European associations of patients affected by rare and/or genetic kidney diseases.

FEDERG Homepage

Latest News

  • Alport Syndrome Patient Information Day on September 6th, 2026! Wednesday, 14, Jan
  • AIRG, 21st Annual Meeting in Madrid, January 17, 2026 Sunday, 11, Jan
  • Members activities Newsletter, volume 2. Tuesday, 16, Sep

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CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation
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Wednesday, 14, Jan
Alport Syndrome Patient Information Day on September 6th, 2026!
Sunday, 11, Jan
AIRG, 21st Annual Meeting in Madrid, January 17, 2026
Tuesday, 16, Sep
Members activities Newsletter, volume 2.
Tuesday, 16, Sep
FEDERG support the adoption of the WHA Resolution on Rare Diseases.
Monday, 9, Jun
FEDERG strongly support the WHA Resolution on rare Diseases
Thursday, 19, Sep
Fighting for our federation Federg f2f Members meeting September 14 Martorell