Found: 7
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Epidemiology of autosomal-dominant polycystic kidney disease: an in-depth clinical study for south-western Germany.
- Published in:
- Nephrology Dialysis Transplantation, 2013, v. 28, n. 6, p. 1472
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- Publication type:
- Article
Age-Related Penetrance of Hereditary Atypical Hemolytic Uremic Syndrome.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 6, p. 639, doi. 10.1111/j.1469-1809.2011.00671.x
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- Publication type:
- Article
Germline Mutations of the TMEM127 Gene in Patients with Paraganglioma of Head and Neck and Extraadrenal Abdominal Sites.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 8, p. E1279, doi. 10.1210/jc.2011-0114
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- Publication type:
- Article
Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry.
- Published in:
- Head & Neck, 2016, v. 38, p. E673, doi. 10.1002/hed.24067
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- Publication type:
- Article
A COL4A5 mutation with glomerular disease and signs of chronic thrombotic microangiopathy.
- Published in:
- 2015
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- Publication type:
- Case Study
Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and <sup>123</sup>I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography.
- Published in:
- Neuroendocrinology, 2015, v. 101, n. 4, p. 321, doi. 10.1159/000381458
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- Publication type:
- Article
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
- Published in:
- Clinical Endocrinology, 2013, v. 79, n. 6, p. 817, doi. 10.1111/cen.12218
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- Publication type:
- Article