about
Pheochromocytoma: implications in tumorigenesis and the actual managementMEN1, MEN4, and Carney Complex: Pathology and Molecular GeneticsNeuroendocrine tumours of the head and neck: anatomical, functional and molecular imaging and contemporary management.Interplay between epigenetics and metabolism in oncogenesis: mechanisms and therapeutic approachesPrologue to the volume: Endocrine tumors and their genetics, a perspective.P.Arg82Leu von Hippel-Lindau (VHL) gene mutation among three members of a family with familial bilateral pheochromocytoma in India: molecular analysis and in silico characterization.Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes.Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and miceCharacterization of two mouse models of metastatic pheochromocytoma using bioluminescence imaging.Recurrence of Phaeochromocytoma and Abdominal Paraganglioma After Initial Surgical InterventionParagangliomas and paraganglioma syndromes.Combined inhibition of mTORC1 and mTORC2 signaling pathways is a promising therapeutic option in inhibiting pheochromocytoma tumor growth: in vitro and in vivo studies in female athymic nude mice.Succinate dehydrogenase expression in breast cancer.Familiar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects.(68)Ga-DOTATATE and (18)F-FDG PET/CT in Paraganglioma and Pheochromocytoma: utility, patterns and heterogeneity.Pheochromocytoma and paraganglioma syndromes: genetics and management update.Genetics of hereditary head and neck paragangliomas.Phaeochromocytoma and Paraganglioma.Reduced succinate dehydrogenase B expression is associated with growth and de-differentiation of colorectal cancer cells.Multidisciplinary management of locally advanced and widely metastatic paraganglioma in a patient with life-threatening compressive symptoms.Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.Case - Bladder paraganglioma in a pediatric patient.Aspiration cytology of primary thyroid paraganglioma.[Rare case of a mesenteric tumor].Malignant phenotype and two SDHD mutations in a family with paraganglioma syndrome type 1.Overexpression of the insulin-like growth factor 1 receptor (IGF-1R) is associated with malignancy in familial pheochromocytomas and paragangliomas.Non-circumferential membranous resection of the trachea for paraganglioma: A case report
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
SDH-related pheochromocytoma and paraganglioma.
@ast
SDH-related pheochromocytoma and paraganglioma.
@en
SDH-related pheochromocytoma and paraganglioma.
@nl
type
label
SDH-related pheochromocytoma and paraganglioma.
@ast
SDH-related pheochromocytoma and paraganglioma.
@en
SDH-related pheochromocytoma and paraganglioma.
@nl
prefLabel
SDH-related pheochromocytoma and paraganglioma.
@ast
SDH-related pheochromocytoma and paraganglioma.
@en
SDH-related pheochromocytoma and paraganglioma.
@nl
P2860
P1476
SDH-related pheochromocytoma and paraganglioma.
@en
P2093
Kathryn S King
Vitaly Kantorovich
P2860
P304
P356
10.1016/J.BEEM.2010.04.001
P50
P577
2010-06-01T00:00:00Z