Ramón Peces

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 7

Top Topics

Polycystic Kidney Disease

Glycemic Control

Top Venues

Molecular genetics & genomic medicine

Clinical kidney journal

BMC medical genetics

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

Publications

Ramón Peces, Carlos Peces, Rocío Mena, Emilio Cuesta, Fe Amalia García-Santiago, Marta Ossorio, Sara Afonso, Pablo Lapunzina, Julián Nevado
Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes. Genes 13 (3) (2022)
Ramón Peces, Rocío Mena, Carlos Peces, Pilar Barruz, Hernando Trujillo, Agustín Carreño, Laura Espinosa, Rafael Selgas, Pablo Lapunzina, Julián Nevado
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. Clinical kidney journal 14 (8) (2021)
Ramón Peces, Rocío Mena, Carlos Peces, Emilio Cuesta, Pablo Lapunzina, Rafael Selgas, Julián Nevado
Birth of two healthy girls following preimplantation genetic diagnosis and gestational surrogacy in a rapidly progressive autosomal dominant polycystic kidney disease case using tolvaptan. Clinical kidney journal 14 (8) (2021)
Ramón Peces, Rocío Mena, Yolanda Martín, Concepción Hernández, Carlos Peces, Dolores Tellería, Emilio Cuesta, Rafael Selgas, Pablo Lapunzina, Julián Nevado
Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2. Molecular genetics & genomic medicine 8 (8) (2020)
Ramón Peces, Rocio Mena, Carlos Peces, Emilio Cuesta, Rafael Selgas, Pilar Barruz, Pablo Lapunzina, Julián Nevado
Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early-onset and fast cyst progression. Clinical genetics 97 (6) (2020)
Ramón Peces, Rocío Mena, Carlos Peces, Fernando Santos-Simarro, Luis Fernández, Sara Afonso, Pablo Lapunzina, Rafael Selgas, Julián Nevado
Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report. Molecular genetics & genomic medicine 7 (4) (2019)
Ramón Peces, Sara Afonso, Carlos Peces, Julián Nevado, Rafael Selgas
Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report. BMC medical genetics 18 (1) (2017)