Carlos Peces

Toledo, CM 45003, Spain

Last Updated: 09/26/2026

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Found 17 publications

A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1.

A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1.

Journal: Genes

Published: August 17, 2023

Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes.

Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes.

Journal: Genes

Published: January 14, 2022

Historical and geographical distribution of the founder mutation c.610G>A; p.Ala204Thr in the CLCNKB gene linked to Bartter syndrome type III in Spain.

Historical and geographical distribution of the founder mutation c.610G>A; p.Ala204Thr in the CLCNKB gene linked to Bartter syndrome type III in Spain.

Journal: Clinical kidney journal

Published: January 25, 2021

Birth of two healthy girls following preimplantation genetic diagnosis and gestational surrogacy in a rapidly progressive autosomal dominant polycystic kidney disease case using tolvaptan.

Birth of two healthy girls following preimplantation genetic diagnosis and gestational surrogacy in a rapidly progressive autosomal dominant polycystic kidney disease case using tolvaptan.

Journal: Clinical kidney journal

Published: October 20, 2020

Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.

Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.

Journal: Molecular genetics & genomic medicine

Published: January 10, 2020

Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early-onset and fast cyst progression.

Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early-onset and fast cyst progression.

Journal: Clinical genetics

Published: December 24, 2019

Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.

Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.

Journal: Molecular genetics & genomic medicine

Published: July 22, 2018

Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report.

Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report.

Journal: BMC medical genetics

Published: February 24, 2017

Autosomal dominant polycystic kidney disease with contralateral renal agenesis.

Autosomal dominant polycystic kidney disease with contralateral renal agenesis.

Journal: Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia

Published: July 29, 2012

A novel and de novo deletion in the OCRL1 gene associated with a severe form of Lowe syndrome.

A novel and de novo deletion in the OCRL1 gene associated with a severe form of Lowe syndrome.

Journal: International urology and nephrology

Published: February 05, 2012

Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuria.

Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuria.

Journal: Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia

Published: December 17, 2011

Giant bilateral renal angiomyolipomas and lymphangioleiomyomatosis presenting after two successive pregnancies successfully treated with surgery and rapamycin.

Giant bilateral renal angiomyolipomas and lymphangioleiomyomatosis presenting after two successive pregnancies successfully treated with surgery and rapamycin.

Journal: TheScientificWorldJournal

Published: July 15, 2011

Showing 1-12 of 17

Last Updated: 09/26/2026