Found: 13
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Heterozygous COL4A3/COL4A4 mutations: the hidden part of the iceberg?
- Published in:
- Nephrology Dialysis Transplantation, 2022, v. 37, n. 12, p. 2398, doi. 10.1093/ndt/gfab334
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- Publication type:
- Article
Vestibular and audiological findings in the Alport syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 10, p. 2345, doi. 10.1002/ajmg.a.61796
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- Publication type:
- Article
Single, Double and Triple Blockade of RAAS in Alport Syndrome: Different Tools to Freeze the Evolution of the Disease.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 21, p. 4946, doi. 10.3390/jcm10214946
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- Publication type:
- Article
Successful medical treatment of EBV smooth muscle tumor in a renal transplant recipient.
- Published in:
- Pediatric Transplantation, 2010, v. 14, n. 8, p. E101, doi. 10.1111/j.1399-3046.2009.01213.x
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- Publication type:
- Article
Alport syndrome and pregnancy: a case series and literature review.
- Published in:
- 2018
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- Publication type:
- journal article
Alport syndrome: the effects of spironolactone on proteinuria and urinary TGF-β1.
- Published in:
- Pediatric Nephrology, 2013, v. 28, n. 9, p. 1837, doi. 10.1007/s00467-013-2490-z
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- Publication type:
- Article
Alport syndrome: the effects of spironolactone on proteinuria and urinary TGF-β1.
- Published in:
- 2013
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- Publication type:
- Journal Article
Urine erythrocyte morphology in patients with microscopic haematuria caused by a glomerulopathy.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 7, p. 1093, doi. 10.1007/s00467-008-0777-2
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- Publication type:
- Article
Dietary prescription based on estimated nitrogen balance during peritoneal dialysis.
- Published in:
- Pediatric Nephrology, 1999, v. 13, n. 3, p. 253, doi. 10.1007/s004670050604
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- Publication type:
- Article
Adequate clinical control of congenital nephrotic syndrome by enalapril.
- Published in:
- Pediatric Nephrology, 1998, v. 12, n. 2, p. 130, doi. 10.1007/s004670050420
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- Publication type:
- Article
Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
- Published in:
- Nephrology Dialysis Transplantation, 2006, v. 21, n. 3, p. 665, doi. 10.1093/ndt/gfi312
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- Publication type:
- Article
Deletion spanning the 5′ ends of both the COL4A5 and COL4A6 genes in a patient with Alport's syndrome and leiomyomatosis.
- Published in:
- Human Mutation, 1994, v. 4, n. 3, p. 195, doi. 10.1002/humu.1380040304
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- Publication type:
- Article
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178630
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- Publication type:
- Article