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Cristina Cea Arestín

Institutions of which they are part

Predoctoral researcher
Kidney Physiopathology
Vall Hebron Institut de Recerca

Cristina Cea Arestín

Institutions of which they are part

Predoctoral researcher
Kidney Physiopathology
Vall Hebron Institut de Recerca

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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