R. Peces

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index1.6kcitations156works3.02yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(26), Renal Diseases and Glomerulopathies(13), Pharmacological Effects and Toxicity Studies(10), Renal function and acid-base balance(10), Biomedical Research and Pathophysiology(10)

Publications154 total

MEC Federation for Seamless Service Continuity in Cross-Border Mobility Scenarios
2024· 3 citedOpen Access
A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1
Genes·2023· 5 citedOpen Access
Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes
Genes·2022· 2 citedOpen Access
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·2021· 2 citedOpen Access
Historical and geographical distribution of the founder mutation c.610G&amp;gt;A; p.Ala204Thr in the <i>CLCNKB</i> gene linked to Bartter syndrome type III in Spain
Clinical Kidney Journal·2021· 1 citedOpen Access
Co‐occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2
Molecular Genetics & Genomic Medicine·2020· 5 citedOpen Access
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·2020· 3 cited
Author response for "Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2. A model of early‐onset and fast cyst progression"
2020
Nutcracker syndrome complicated by left renal vein thrombosis and resolution with anticoagulation: A case report and review of the literature
Nephrology and Renal Diseases·2020· 2 citedOpen Access
Donnai– Barrow Syndrome in Two Sisters with a Homozygous LRP2 Mutation and Renal Dysfunction. Integral Management of the Disease with Review of the Literature.
2020Open Access
Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the <i>AQP2</i> gene. A case report
Molecular Genetics & Genomic Medicine·2019· 10 citedOpen Access
Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report
BMC Medical Genetics·2017· 6 citedOpen Access
Everolimus safety and efficacy for renal angiomyolipomas associated with tuberous sclerosis complex: a Spanish expanded access trial
Orphanet Journal of Rare Diseases·2016· 19 citedOpen Access
MP039THE EFFECT OF EVEROLIMUS IN PATIENTS WITH RENAL ANGIOMYOLIPOMA ASSOCIATED WITH TUBEROUS SCLEROSIS COMPLEX
Nephrology Dialysis Transplantation·2016Open Access
Estudio multihospitalario sobre la membrana de triacetato de celulosa en hemodiálisis
2016Open Access
Economic Burden Of Adpkd From The Spanish Health System And Patient’s Perspective: Advantages Of Delaying Dialysis
Value in Health·2015Open Access
Development Of A Model To Predict Disease Progression In Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Value in Health·2014Open Access
Development of a model to predict disease progression in autosomal dominant polycystic kidney disease (ADPKD)
2014
RENAL DEVELOPMENT AND CYSTIC DISEASES
Nephrology Dialysis Transplantation·2014
Malignancy and chronic renal failure.
PubMed·2012· 8 cited
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Frequent Co-authors

M. de la Torre(9), Carlos Peces(8), Rafael Selgas(7), Roberto Alcázar Arroyo(5), José Miguel Urra(5), Pilar Ruíz-Seco(4), Rafael A. Navascués(3), A Pobes(3), Julio Alvarez(3), Manuel Gorostidi(3), Emilio Cuesta-López(3), Miguel Seco(2), J.R. Riera(2), Carlos López‐Larrea(2), A. Laurés(2), M.I. Rivera Rodríguez(2), V. Perez-Duenas(2), Cristina Vega-Cabrera(2), P Ablanedo(2), J. Baltar(2)