The clinical presentation (symptoms and signs) of sporadic and familial chromaffin cell tumours (phaeochromocytomas and paragangliomas).

The clinical presentation (symptoms and signs) of sporadic and familial chromaffin cell tumours (phaeochromocytomas and paragangliomas).

Xehetasun bibliografikoak
Egile Nagusiak:	Kaltsas, G, Papadogias, D, Grossman, AB
Formatua:	Journal article
Hizkuntza:	English
Argitaratua:	2004

Antzeko izenburuak

The diagnosis and management of malignant phaeochromocytoma and paraganglioma.
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The clinical genetics of phaeochromocytoma and paraganglioma
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Treatment of malignant phaeochromocytoma, paraganglioma and carcinoid tumours with 131I-metaiodobenzylguanidine.
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Argitaratua: (1993)

Naloxone provokes catecholamine release in phaeochromocytomas and paragangliomas.
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Argitaratua: (1986)

Treatment of metastatic carcinoid tumours, phaeochromocytoma, paraganglioma and medullary carcinoma of the thyroid with (131)I-meta-iodobenzylguanidine [(131)I-mIBG].
nork: Mukherjee, J, et al.
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Dopamine-secreting phaeochromocytomas and paragangliomas: clinical features and management
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Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.
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Treatment of advanced neuroendocrine tumours with radiolabelled somatostatin analogues.
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Phaeochromocytoma and Paraganglioma Excision Involving the Great Vessels
nork: U. Srirangalingam, et al.
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Using parenclitic networks on phaeochromocytoma and paraganglioma tumours provides novel insights on global DNA methylation
nork: Dimitria Brempou, et al.
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Personalized diagnostics of chromaffin tumors (pheochromocytoma, paraganglioma) in oncoendocrinology
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A Laboratory Medicine Perspective on the Investigation of Phaeochromocytoma and Paraganglioma
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Contrasting clinical manifestations of SDHB and VHL associated chromaffin tumours.
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Recent advances in radiological and radionuclide imaging and therapy of neuroendocrine tumours.
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Phaeochromocytoma crisis presenting with profound hypoglycaemia and subsequent hypertension.
nork: Frankton, S, et al.
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Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.
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Predictors of outcome in phaeochromocytomas and paragangliomas [version 1; referees: 3 approved]
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A comprehensive characterisation of phaeochromocytoma and paraganglioma tumours through histone protein profiling, DNA methylation and transcriptomic analysis genome wide
nork: Prodromos Chatzikyriakou, et al.
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Novel and evolving therapies in the treatment of malignant phaeochromocytoma: experience with the mTOR inhibitor everolimus (RAD001).
nork: Druce, MR, et al.
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The challenge of improving the diagnostic yield from metanephrine testing in suspected phaeochromocytoma and paraganglioma
nork: Samsudin, Intan Nureslyna, et al.
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Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis
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Genetic testing and immunohistochemistry for SDHB in phaeochromocytoma-paraganglioma syndromes: the South Australian experience
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The dangers of unopposed beta-adrenergic blockade in phaeochromocytoma.
nork: Sheaves, R, et al.
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Combined blockade of signalling pathways shows marked anti-tumour potential in phaeochromocytoma cell lines.
nork: Nölting, S, et al.
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The use of temozolomide in paediatric metastatic phaeochromocytoma/paraganglioma: A case report and literature review
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Unilateral Sporadic Carotid Paraganglioma
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Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas.
nork: Dahia, P, et al.
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Malignant pituitary tumours.
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Rare presentation of collapse and cardiomyopathy in phaeochromocytoma
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Phaeochromocytoma Crisis: Two Cases of Undiagnosed Phaeochromocytoma Presenting after Elective Nonrelated Surgical Procedures
nork: P. C. Johnston, et al.
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Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
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Peptide Receptor Radionuclide Treatment and (131)I-MIBG in the management of patients with metastatic/progressive phaeochromocytomas and paragangliomas
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Familial paraganglioma: a novel presentation of a case and response to therapy with radiolabelled MIBG.
nork: Lawrence, J, et al.
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Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours.
nork: Kaltsas, G, et al.
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Intracerebral haemorrhage: A rare presentation of phaeochromocytoma
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Treatment of metastatic pheochromocytoma and paraganglioma with I-131-meta-iodobenzylguanidine (MIBG)
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A Rare Case: Sporadic Bladder Paraganglioma
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Programmed cell death ligands expression in phaeochromocytomas and paragangliomas: Relationship with the hypoxic response, immune evasion and malignant behavior
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MIBG scans for phaeochromocytoma: time to abandon the technique?
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