Paula Adriana Rozenfeld (Paula A Rozenfeld, Rozenfeld Paula)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Topics

Transforming Growth Factor

Hypertrophic Cardiomyopathy

Chronic Kidney Disease

Top Venues

Journal of nephrology

Molecular genetics & genomic medicine

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Constanza Bondar, Maria de Los Angeles de Bolla, Pablo Neumann, Antonio Pisani, Sandro Feriozzi, Paula Adriana Rozenfeld
Pathogenic pathways of renal damage in Fabry nephropathy: interplay between immune cell infiltration, apoptosis and fibrosis. Journal of nephrology 37 (3) (2024)
Constanza Bondar, Maria de Los Angeles de Bolla, Pablo Neumann, Antonio Pisani, Sandro Feriozzi, Paula Adriana Rozenfeld
Pathogenic pathways of renal damage in Fabry nephropathy: interplay between immune cell infiltration, apoptosis and fibrosis. Journal of nephrology (2024)
Maximiliano Emanuel Ormazabal, Eleonora Pavan, Emilio Vaena, Dania Ferino, Jessica Biasizzo, Juan Marcos Mucci, Fabrizio Serra, Adriana Cifù, Maurizio Scarpa, Paula Adriana Rozenfeld, Andrea Elena Dardis
Exploring the Pathophysiologic Cascade Leading to Osteoclastogenic Activation in Gaucher Disease Monocytes Generated via CRISPR/Cas9 Technology. International journal of molecular sciences 24 (13) (2023)
Choua Martin, Neumann Pablo, Quieto Pedro, Paula Adriana Rozenfeld, null null
Screening for Fabry disease in Argentina in male patients with chronic kidney disease at all stages. Journal of nephrology 35 (9) (2022)
Paula Adriana Rozenfeld, Francisca M Masllorens, Norma Roa, Fernanda Rodriguez, Mariela Bonnano, Carolina Yvorra, Romina Ceci
Fabry pedigree analysis: A successful program for targeted genetic approach. Molecular genetics & genomic medicine 7 (7) (2019)
Andrea N Crivaro, Juan M Mucci, Constanza M Bondar, Maximiliano E Ormazabal, Romina Ceci, Calogera Simonaro, Paula Adriana Rozenfeld
Efficacy of pentosan polysulfate in in vitro models of lysosomal storage disorders: Fabry and Gaucher Disease. PloS one 14 (5) (2019)