✦ LIBER ✦

Pheochromocytoma in von hippel-lindau disease: Distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2

✍ Scribed by Christian A. Koch; David Mauro; McClellan M. Walther; W. Marston Linehan; Alexander O. Vortmeyer; Ronald Jaffe; Karel Pacak; George P. Chrousos; Zhengping Zhuang; Irina A. Lubensky

Book ID: 111638431
Publisher: Springer US
Year: 2002
Tongue: English
Weight: 678 KB
Volume: 13
Category: Article
ISSN: 1046-3976
DOI: 10.1385/ep:13:1:17

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Transcriptional Regulation of Phenyletha

Transcriptional Regulation of Phenylethanolamine N-Methyltransferase in Pheochromocytomas from Patients with von Hippel–Lindau Syndrome and Multiple Endocrine Neoplasia Type 2

✍ THANH-TRUC HUYNH; KAREL PACAK; DONA L. WONG; W. MARSTON LINEHAN; DAVID S. GOLDST 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

Genotype–phenotype correlations of pheoc

Genotype–phenotype correlations of pheochromocytoma in two large von Hippel–Lindau (VHL) type 2A kindreds with different missense mutations

✍ Sarah M. Nielsen; Wendy S. Rubinstein; Darcy L. Thull; Michaele J. Armstrong; El 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 129 KB 👁 2 views

## Abstract Von Hippel–Lindau (VHL) disease type 2A is an inherited tumor syndrome characterized by predisposition to pheochromocytoma (pheo), retinal hemangioma (RA), and central nervous system hemangioblastoma (HB). Specific VHL subtypes display genotype–phenotype correlations but, unlike other f

Biochemical diagnosis, localization and

Biochemical diagnosis, localization and management of pheochromocytoma: focus on multiple endocrine neoplasia type 2 in relation to other hereditary syndromes and sporadic forms of the tumour

✍ K. PACAK; I. ILIAS; K. T. ADAMS; G. EISENHOFER 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 192 KB