Found: 17
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Expression of Hypoxia-Inducible Factors, Regulators, and Target Genes in Congenital Diaphragmatic Hernia Patients.
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- Pediatric & Developmental Pathology, 2011, v. 14, n. 5, p. 384, doi. 10.2350/09-09-0705-OA.1
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- Article
ACTH-independent macronodular adrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro responses to hormonal stimuli and coupling of arginine-vasopressin type 1a receptor to 11β-hydroxylase.
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- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-142
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- Article
Conditional Pten knock-out mice: a model for metastatic phaeochromocytoma.
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- Journal of Pathology, 2009, v. 217, n. 4, p. 597, doi. 10.1002/path.2492
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- Article
Expression of Contactin 4 Is Associated With Malignant Behavior in Pheochromocytomas and Paragangliomas.
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- 2017
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- Publication type:
- journal article
Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis.
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- 2016
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- journal article
Parathyroid Hormone-Related Peptide (PTHrP) Secretion by Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs): Clinical Features, Diagnosis, Management, and Follow-Up.
- Published in:
- 2014
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- Publication type:
- Journal Article
SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas.
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- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. E1472, doi. 10.1210/jc.2011-1043
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- Article
p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas.
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- 2003
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- Publication type:
- journal article
Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.
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- 2009
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- Publication type:
- journal article
Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 6, p. 1938, doi. 10.1210/jc.2009-0354
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- Article
Frequent Genetic Changes in Childhood Pheochromocytomas.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 166, doi. 10.1196/annals.1353.017
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- Article
The Occurrence of SDHB Gene Mutations in Pheochromocytoma.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 177, doi. 10.1196/annals.1353.018
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- Article
Predictors of treatment response in lymphogenic metastasized papillary thyroid cancer: a histopathological study.
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- European Journal of Endocrinology, 2024, v. 190, n. 5, p. 374, doi. 10.1093/ejendo/lvae048
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- Article
Regulation of steroidogenesis in a primary pigmented nodular adrenocortical disease-associated adenoma leading to virilization and subclinical Cushing's syndrome.
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- European Journal of Endocrinology, 2013, v. 167, n. 1, p. 67, doi. 10.1530/EJE-12-0594
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- Article
Peptide receptor radionuclide therapy in patients with medullary thyroid carcinoma: predictors and pitfalls.
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- 2019
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- Publication type:
- journal article
Microarray‐based CGH of sporadic and syndrome‐related pheochromocytomas using a 0.1–0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 1, p. 83, doi. 10.1002/gcc.20268
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- Article
European experience with the Afirma Gene Expression Classifier for indeterminate thyroid nodules: A clinical utility study in the Netherlands.
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- Head & Neck, 2023, v. 45, n. 9, p. 2227, doi. 10.1002/hed.27472
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- Article