Found: 12
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Investigation of the human ANP gene in type 1 diabetic nephropathy: case-control and follow-up studies.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Periodontal (formerly type VIII) Ehlers–Danlos syndrome: Description of 13 novel cases and expansion of the clinical phenotype.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 2, p. 206, doi. 10.1111/cge.13972
- By:
- Publication type:
- Article
Liddle syndrome phenotype in an octogenarian.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Liddle Syndrome Phenotype in an Octogenarian.
- Published in:
- Journal of Clinical Hypertension, 2015, v. 17, n. 1, p. 59, doi. 10.1111/jch.12450
- By:
- Publication type:
- Article
Report of a family with two different hereditary diseases leading to early nephrocalcinosis.
- Published in:
- 2008
- By:
- Publication type:
- Report
Abnormalities of ventricular repolarization in mitral valve prolapse.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Abnormalities of Ventricular Repolarization in Mitral Valve Prolapse.
- Published in:
- Annals of Noninvasive Electrocardiology, 2005, v. 10, n. 3, p. 297, doi. 10.1111/j.1542-474X.2005.00630.x
- By:
- Publication type:
- Article
Carotid Stiffness Assessment With Ultrafast Ultrasound Imaging in Case of Bicuspid Aortic Valve.
- Published in:
- Frontiers in Physiology, 2019, v. 10, p. 1, doi. 10.3389/fphys.2019.01330
- By:
- Publication type:
- Article
Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism.
- Published in:
- Human Mutation, 2007, v. 28, n. 1, p. 33, doi. 10.1002/humu.20371
- By:
- Publication type:
- Article
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2009, v. 24, n. 5, p. 1455, doi. 10.1093/ndt/gfn689
- By:
- Publication type:
- Article
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelmans syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 10, p. 3120, doi. 10.1093/ndt/gfn229
- By:
- Publication type:
- Article
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2077, doi. 10.1093/hmg/6.12.2077
- By:
- Publication type:
- Article