Carlos Peces

Universitat de Lleida — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

9h-index270citations51works0.02yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(14), Pediatric Urology and Nephrology Studies(8), Renal Diseases and Glomerulopathies(7), Renal and related cancers(6), Biomedical Research and Pathophysiology(5)

Publications51 total

Periportal cuffing as an ultrasound sign of myeloproliferative syndrome
Anales de Pediatría (English Edition)·2024Open Access
A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1
Genes·2023· 5 citedOpen Access
Vesícula biliar multiseptada en paciente pediátrico
Atención Primaria·2023Open 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
Manguito periportal como signo ecográfico de síndrome mieloproliferativo
Anales de Pediatría·2020Open 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
Diagnóstico ecográfico de catarata
Anales de Pediatría·2020· 1 citedOpen Access
Tortícolis como forma de presentación de quiste de la bolsa de Blake. Diagnóstico ecográfico en atención primaria
Archivos Argentinos de Pediatria·2020Open Access
Diagnóstico ecográfico de craneosinostosis en Atención Primaria
Archivos Argentinos de Pediatria·2020Open Access
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
Ecografía clínica en la infección del trato urinario
Anales de Pediatría·2019· 1 citedOpen 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
Economic Burden Of Adpkd From The Spanish Health System And Patient’s Perspective: Advantages Of Delaying Dialysis
Value in Health·2015Open Access
A novel and de novo deletion in the OCRL1 gene associated with a severe form of Lowe syndrome
International Urology and Nephrology·2012· 6 cited
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Frequent Co-authors

R. Peces(40), Rafael Selgas(25), Emilio Cuesta(11), Julián Nevado(11), Pablo Lapunzina(9), Rocío Mena(8), Emilio Cuesta-López(6), V. Perez-Duenas(5), Cristina Vega-Cabrera(5), Sebastián Azorín(5), Luis Ortiz-González(5), Luis Ortiz-Peces(5), Cristina Vega(3), Elena González(3), José Gimeno Sacristán(3), Sara Afonso(3), Pilar Barrúz(3), Rafáel Sánchez(3), Ana Aguilar(2), Enrique J. Fernández(2)