R. Muley

Renal pathology in children with mitochondrial diseases

J. Arenas, Miguel Ángel Martín, M. García-Silva, 2005, Pediatric Nephrology.

Urinary excretion of platelet-activating factor in human and experimental nephrosis.

A. Ortiz, J. Egido, J. Plaza, 1996, Nephrology, Dialysis and Transplantation.

Increase of tumour necrosis factor α synthesis and gene expression in peripheral blood mononuclear cells of children with idiopathic nephrotic syndrome

J. Egido, R. Muley, E. González, 1994, European journal of clinical investigation.

Urinary excretion of platelet-activating factor in human and experimental nephrosis.

A. Ortiz, J. Egido, J. Plaza, 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Improvement in growth after 1 year of growth hormone therapy in well-nourished infants with growth retardation secondary to chronic renal failure: results of a multicenter, controlled, randomized, open clinical trial.

J. Argente, G. Ariceta, F. Santos, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

G. Ariceta, F. Claverie-Martin, F. Santos, 2013, PloS one.

TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.

P. Fernández-Llama, E. Ars, J. Rosell, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Dent’s disease: Identification of seven new pathogenic mutations in the CLCN5 gene

G. Ariceta, F. Claverie-Martin, M. García-Ramírez, 2013, Journal of Pediatric Genetics.

Ifosfamide-induced renal tubular defect.

C. Melero, J. Vivanco, J. Vara, 1994, Medical and pediatric oncology.

Pyelic benign fibroepithelial polyp in childhood: a case report.

J. Matute, R. Muley, A. Gómez Fraile, 1993, Journal of pediatric surgery.

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

J. Arenas, Y. Campos, A. Cabello, 1995, Pediatric neurology.

A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome

J. Arenas, Miguel Ángel Martín, A. Delmiro, 2013, BMC Nephrology.