High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing - Wikidata - awgldk - TriplyDB

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

http://www.wikidata.org/entity/Q28258042

about

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5 LB100, a small molecule inhibitor of PP2A with potent chemo- and radio-sensitizing potential Physiological consequences of complex II inhibition for aging, disease, and the mKATP channel An update on the genetics of pheochromocytoma Pharmacologic modulation of serine/threonine phosphorylation highly sensitizes PHEO in a MPC cell and mouse model to conventional chemotherapy Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience.Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas Anti-cancer potential of MAPK pathway inhibition in paragangliomas-effect of different statins on mouse pheochromocytoma cells.A case of (123)I-MIBG scintigram-negative functioning pheochromocytoma: immunohistochemical and molecular analysis with review of literature NF-κB inhibition significantly upregulates the norepinephrine transporter system, causes apoptosis in pheochromocytoma cell lines and prevents metastasis in an animal model.SDH-related pheochromocytoma and paraganglioma.Solid tumors associated with multiple endocrine neoplasias.New imaging approaches to phaeochromocytomas and paragangliomas.Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment The size of the primary tumor and age at initial diagnosis are independent predictors of the metastatic behavior and survival of patients with SDHB-related pheochromocytoma and paraganglioma: a retrospective cohort study Clinical experiences of pheochromocytoma in Korea.Metastatic paraganglioma.Paraganglioma in a young patient with asymptomatic severe hypertension: a case report and review of the literature.An N-terminal truncated carboxypeptidase E splice isoform induces tumor growth and is a biomarker for predicting future metastasis in human cancers.Genetic testing for pheochromocytoma.Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma.Metastatic pheochromocytoma: does the size and age matter?Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma.Plasma methoxytyramine: a novel biomarker of metastatic pheochromocytoma and paraganglioma in relation to established risk factors of tumour size, location and SDHB mutation status.The genetic basis of pheochromocytoma and paraganglioma: implications for management Updated and new perspectives on diagnosis, prognosis, and therapy of malignant pheochromocytoma/paraganglioma.Phaeochromocytoma: a catecholamine and oxidative stress disorder.Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl.The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer False-negative ¹²³I-MIBG SPECT is most commonly found in SDHB-related pheochromocytoma or paraganglioma with high frequency to develop metastatic disease.Disentangling of Malignancy from Benign Pheochromocytomas/Paragangliomas Structural basis for malfunction in complex II.Pheochromocytoma - update on disease management.Clinical aspects of SDHx-related pheochromocytoma and paraganglioma Successful chemotherapy of hepatic metastases in a case of succinate dehydrogenase subunit B-related paraganglioma.

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P2860

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

http://www.wikidata.org/entity/Q28258042

description

2006 nî lūn-bûn

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2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年论文

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name

High frequency of SDHB germlin ...... plications for genetic testing

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High frequency of SDHB germlin ...... plications for genetic testing

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High frequency of SDHB germlin ...... plications for genetic testing

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High frequency of SDHB germlin ...... plications for genetic testing

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High frequency of SDHB germlin ...... plications for genetic testing

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The Journal of Clinical Endocrinology and Metabolism

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High frequency of SDHB germlin ...... plications for genetic testing

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Frederieke M Brouwers

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Graeme Eisenhofer

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Jeffrey A Kant

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Jessica J Tao

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10.1210/JC.2006-0423

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