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Gema Ariceta Iraola

Institutions of which they are part

Head of group
Kidney Physiopathology
Vall Hebron Institut de Recerca

Gema Ariceta Iraola

Institutions of which they are part

Head of group
Kidney Physiopathology
Vall Hebron Institut de Recerca

Projects

Biología de sistemas para el descubrimiento de mecanismos fisiopatológicos y dianas rerapéuticas en la hipomagnesimia familiarr primaria con hipercalciuria y nefrocalcinosis.

IP: Gema Ariceta Iraola
Collaborators: Alejandro Cruz Gual, Marina Muñoz López, Mercedes López González
Funding agency: Instituto de Salud Carlos III
Funding: 171820
Reference: PI18/01107
Duration: 01/01/2019 - 30/06/2023

ERK-REG: ERKNet Registry for Rare Kidney Diseases

IP: Gema Ariceta Iraola
Collaborators: -
Funding agency: Ex. Agency for Health Consumers (EAHC)-CHAFEA
Funding: 38871
Reference: ERK-REG_3HP2017
Duration: 01/01/2018 - 31/12/2020

Incorporació Dr. Daniel Serón a la RETICS en Malalties renals

IP: Daniel Serón Micas
Collaborators: Gema Ariceta Iraola, Joan López Hellin, Incorporació Dr. Daniel Serón a la RETICS en Malalties renals, Ramón Vilalta Casas, Francesc Moreso Mateos, Enric Trilla Herrera, Natalia Ramos Terrades, David Lorente García, Maria Jose Soler Romeo, Meritxell Ibernon Vilaró, Joana Sellarés Roig, María Eugenia Espinel Garuz, Luis Enrique Lara Moctezuma, Irene Agraz Pamplona, Marina Muñoz López, Irina Betsabe Torres Rodriguez, Luis Augusto Castro Sáder, Manel Perelló Carrascosa
Funding agency: Instituto de Salud Carlos III
Funding: 102300
Reference: RD16/0009/0030
Duration: 01/01/2017 - 31/12/2021

Patologia Cel·lular (GRC)

IP: Patologia Cel·lular (GRC)
Collaborators: Gema Ariceta Iraola, Joan López Hellin, Ramón Vilalta Casas, Alvaro Domingo Madrid Aris, Francesc Moreso Mateos, Enric Trilla Herrera, Natalia Ramos Terrades, David Lorente García, Meritxell Ibernon Vilaró, Joana Sellarés Roig, Daniel Serón Micas, María Eugenia Espinel Garuz, Luis Enrique Lara Moctezuma, Irene Agraz Pamplona, Marina Muñoz López, Irina Betsabe Torres Rodriguez, Carles Xavier Raventós Busquets, María Asunción Galicia Basart, Manel Perelló Carrascosa, M Antonieta Azancot Rivero, M Antonieta Azancot Rivero
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding:
Reference: 2014 SGR 667
Duration: 01/01/2014 - 31/12/2016

Related news

The work identifies variants in genes such as NFU1 that, combined with the disease-causing mutation, can accelerate kidney deterioration.

The communication is part of a study aimed at identifying the mechanisms of progression of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis, a rare disease that affects the kidneys.

"Patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis present miRNA profiles in urinary extracellular vesicles associated with disease progression" was the awarded work.

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