Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas. - Wikidata - wikimedia - TriplyDB

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.

http://www.wikidata.org/entity/Q34947066

about

Pheochromocytomas and Paragangliomas: Clinical and Genetic Approaches 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5 An update on the genetics of pheochromocytoma Molecular markers of paragangliomas/pheochromocytomas Paragangliomas/Pheochromocytomas: clinically oriented genetic testing Systematic genetic screening in a prospective group of Danish patients with pheochromocytoma.MicroRNA expression profiling in benign (sporadic and hereditary) and recurring adrenal pheochromocytomas.Current approaches and recent developments in the management of head and neck paragangliomas.Metastatic paraganglioma.Age at diagnosis of pheochromocytoma differs according to catecholamine phenotype and tumor location.Genetic testing for pheochromocytoma.Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma.A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism.Paraganglioma Presenting as Postpartum Fever of Unknown Origin.Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden.Updated and new perspectives on diagnosis, prognosis, and therapy of malignant pheochromocytoma/paraganglioma.Subclinical phaeochromocytoma.False-negative ¹²³I-MIBG SPECT is most commonly found in SDHB-related pheochromocytoma or paraganglioma with high frequency to develop metastatic disease.Current and future anatomical and functional imaging approaches to pheochromocytoma and paraganglioma.Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad.Clinical Next Generation Sequencing for Precision Medicine in Cancer.Genotype and tumor locus determine expression profile of pseudohypoxic pheochromocytomas and paragangliomas Role of hypoxia and HIF2α in development of the sympathoadrenal cell lineage and chromaffin cell tumors with distinct catecholamine phenotypic features.Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling.The approach to the patient with paraganglioma.Hypoxia-inducible factor signaling in pheochromocytoma: turning the rudder in the right direction.Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours.Familial pheochromocytomas and paragangliomas.Neuroendocrine tumors and tumor syndromes in childhood.18F-FDG PET/CT as a predictor of hereditary head and neck paragangliomas Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.Screening for pheochromocytomas and paragangliomas.Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.Hereditary pheochromocytoma and paraganglioma.Cancer genomics and inherited risk.Genetic status determines (18) F-FDG uptake in pheochromocytoma/paraganglioma.Genotype-phenotype correlation in paediatric pheochromocytoma and paraganglioma: a single centre experience from India.Precision medicine in pheochromocytoma and paraganglioma: current and future concepts.

P2860

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P2860

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.

http://www.wikidata.org/entity/Q34947066

description

2009 nî lūn-bûn

@nan

2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի փետրվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@ast

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@en

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@nl

type

label

Clinically guided genetic scre ...... nonfunctional paragangliomas.

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Clinically guided genetic scre ...... nonfunctional paragangliomas.

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Clinically guided genetic scre ...... nonfunctional paragangliomas.

@nl

prefLabel

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@ast

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@en

Clinically guided genetic scre ...... nonfunctional paragangliomas.

@nl

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P356

P1433

The Journal of Clinical Endocrinology and Metabolism

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Clinically guided genetic scre ...... nonfunctional paragangliomas.

@en

P2093

Alessandra Bacca

http://www.w3.org/2001/XMLSchema#string

Bernadette Biondi

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Erika Grossrubatscher

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Franco Veglio

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Gianpaolo Bernini

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Giorgio Arnaldi

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Giuseppe Di Trapani

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Italian Pheochromocytoma/Paraganglioma Network

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Luigi Mori

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Mara Giacchè

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P304

1541-1547

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10.1210/JC.2008-2419

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5

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94

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Giuseppe Opocher

Massimo Mannelli

Claudio Letizia

Maurizio Castellano

Massimo Terzolo

Francesca Schiavi

Giuseppe Reimondo

Maria Rosaria Ambrosio

Annamaria Colao

Gilberta Giacchetti

P577

2009-02-17T00:00:00Z

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P698

19223516

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P921

phaeochromocytoma