Found: 9
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Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Tres casos de gammapatía monoclonal de significado renal postrasplante renal: nefropatía c3 de novo.
- Published in:
- Nefrologia, 2019, v. 39, n. 2, p. 198, doi. 10.1016/j.nefro.2018.03.008
- By:
- Publication type:
- Article
Nefropatía asociada a mutación del gen MYH9.
- Published in:
- Nefrologia, 2019, v. 39, n. 2, p. 133, doi. 10.1016/j.nefro.2018.08.008
- By:
- Publication type:
- Article
A review on autosomal dominant tubulointerstitial kidney disease.
- Published in:
- Nefrologia, 2017, v. 37, n. 3, p. 235, doi. 10.1016/j.nefro.2016.10.024
- By:
- Publication type:
- Article
Sangrado de angiomiolipoma renal en paciente con síndrome de genes contiguos (TSC2/PKD1) tras 17 años de tratamiento renal sustitutivo.
- Published in:
- Nefrologia, 2017, v. 37, n. 1, p. 87, doi. 10.1016/j.nefro.2016.04.007
- By:
- Publication type:
- Article
Nefropatía intersticial crónica familiar con hiperuricemia causada por el gen UMOD.
- Published in:
- Nefrologia, 2013, v. 33, n. 4, p. 587, doi. 10.3265/Nefrologia.pre2013.Apr.11960
- By:
- Publication type:
- Article
Familial chronic interstitial nephropathy with hyperuricaemia caused by the UMOD gene.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Acute Renal Failure Secondary to an Unusual Familial Metabolic Myopathy.
- Published in:
- Nephron, 2021, v. 145, n. 2, p. 199, doi. 10.1159/000512666
- By:
- Publication type:
- Article
Recombinant PTH associated with hypercalcaemia and renal failure.
- Published in:
- 2013
- By:
- Publication type:
- Case Study