Xosé M.
Lens Neo
Publicacións (56) Publicacións de Xosé M. Lens Neo
2013
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A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis
Kidney International, Vol. 83, Núm. 1, pp. 153-159
2008
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Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the rat
European Journal of Medical Genetics, Vol. 51, Núm. 4, pp. 325-331
2007
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Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease
Molecular Genetics and Metabolism, Vol. 92, Núm. 1-2, pp. 160-167
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Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1
Nephrology Dialysis Transplantation, Vol. 22, Núm. 6, pp. 1567-1577
2005
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A comparative study of three kidney biomarker tests in autosomal-dominant polycystic kidney disease
Kidney International, Vol. 68, Núm. 3, pp. 948-954
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A novel pattern of mutation in uromodulin disorders: Autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease
American Journal of Kidney Diseases, Vol. 46, Núm. 1, pp. 52-57
2004
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Comparison between siblings and twins supports a role for modifier genes in ADPKD
Kidney International, Vol. 66, Núm. 6, pp. 2132-2136
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Homozygosity for uromodulin disorders: FJHN and MCKD-type 2
Kidney International, Vol. 66, Núm. 2, pp. 558-563
2003
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Autosomal Recessive Alport's Syndrome and Benign Familial Hematuria Are Collagen Type IV Diseases
American Journal of Kidney Diseases, Vol. 42, Núm. 5, pp. 952-959
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ENOS polymorphism and renal disease progression in autosomal dominant polycystic kidney disease [3] (multiple letters)
American Journal of Kidney Diseases
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Poliquistosis renal autosómica recesiva
Nefrologia, Vol. 23, Núm. SUPPL.1, pp. 23-28
2002
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Los nefrólogos y la poliquistosis renal.
Nefrologia
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Modifier effect of ENOS in autosomal dominant polycystic kidney disease
Human Molecular Genetics, Vol. 11, Núm. 3, pp. 229-241
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Mutations in the COL4A4 and COL4A3 genes cause familial benign hematuria
Journal of the American Society of Nephrology, Vol. 13, Núm. 5, pp. 1248-1254
2000
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Long-term anti-proteinuric effect of Losartan in renal transplant recipients treated for hypertension
Nephrology Dialysis Transplantation, Vol. 15, Núm. 1, pp. 82-86
1999
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Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease
Journal of the American Society of Nephrology, Vol. 10, Núm. 11, pp. 2342-2351
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Cortical nephrocalcinosis induced by extracorporeal shock wave lithotripsy [3]
Nephron
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Renal artery rupture secondary to pretransplantation Candida contamination of the graft in two different recipients.
American journal of kidney diseases : the official journal of the National Kidney Foundation, Vol. 33, Núm. 1
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Secondary hyperparathyroidism exacerbation: A rare side-effect of interferon-alpha?
Clinical Nephrology, Vol. 51, Núm. 4, pp. 248-251
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Utilidad de la anfotericina B liposomial (AmBisome®) en la aspergilosis invasiva
Nefrologia