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International Journal of Surgical Pathology|October 17, 2006
Critical comparison of 31 commercially available digital slide systems in pathologyMarcial García Rojo, Gloria Bueno García, Carlos Peces Mateos, et al.
International Urology and Nephrology|May 8, 2010
Octreotide reduces hepatic, renal and breast cystic volume in autosomal-dominant polycystic kidney diseaseRamón Peces, Emilio Cuesta-López, Carlos Peces, et al.
Clinical Genetics|March 14, 2020
Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early-onset and fast cyst progressionRamón Peces, Rocio Mena, Carlos Peces, et al.
Diagnostic Pathology|August 5, 2008
Reading virtual slide using web viewers: results of subjective experience with three different solutionsMarcial García Rojo, Antonio J Gallardo, Lucía González, et al.
Genes|October 28, 2023
A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of <i>WNK1</i>Ramón Peces, Carlos Peces, Laura Espinosa, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 29, 2010
Low-dose rapamycin reduces kidney volume angiomyolipomas and prevents the loss of renal function in a patient with tuberous sclerosis complexRamón Peces, Carlos Peces, Emilio Cuesta-López, et al.
Thescientificworldjournal|May 10, 2011
Nephrotic syndrome and idiopathic membranous nephropathy associated with autosomal-dominant polycystic kidney diseaseRamón Peces, Jorge Martínez-Ara, Carlos Peces, et al.
Molecular Genetics & Genomic Medicine|February 21, 2019
Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case reportRamón Peces, Rocío Mena, Carlos Peces, et al.
Molecular Genetics & Genomic Medicine|June 14, 2020
Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2Ramón Peces, Rocío Mena, Yolanda Martín, et al.
Genes|March 25, 2022
Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman SyndromesRamón Peces, Carlos Peces, Rocío Mena, et al.
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