Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 217,273,815 papers from all fields of science
Search
Sign In
Create Free Account
Paraganglioma
Known as:
PARAGANGLIOMATA
, Paragangliomas
, Paraganglioma, Gangliocytic
Expand
A benign or malignant neoplasm arising from paraganglia located along the sympathetic or parasympathetic nerves. Infrequently, it may arise outside…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
31 relations
Aphonia
Autonomic nervous system
Autosomal dominant inheritance
Blood supply aspects
Expand
Narrower (2)
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMAS 2 (disorder)
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Paraganglioma and phaeochromocytoma: from genetics to personalized medicine
J. Favier
,
L. Amar
,
A. Gimenez-Roqueplo
Nature Reviews Endocrinology
2015
Corpus ID: 26205361
Paragangliomas and phaeochromocytomas are neuroendocrine tumours whose pathogenesis and progression are very strongly influenced…
Expand
Review
2014
Review
2014
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
J. Lenders
,
Q. Duh
,
+6 authors
W. Young
Journal of Clinical Endocrinology and Metabolism
2014
Corpus ID: 668884
OBJECTIVE The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). PARTICIPANTS The…
Expand
Review
2014
Review
2014
Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity
P. Dahia
Nature Reviews. Cancer
2014
Corpus ID: 31457232
The neuroendocrine tumours pheochromocytomas and paragangliomas carry the highest degree of heritability in human neoplasms…
Expand
Highly Cited
2010
Highly Cited
2010
SDHA is a tumor suppressor gene causing paraganglioma.
N. Burnichon
,
J. Briere
,
+11 authors
A. Gimenez-Roqueplo
Human Molecular Genetics
2010
Corpus ID: 17031471
Mitochondrial succinate-coenzyme Q reductase (complex II) consists of four subunits, SDHA, SDHB, SDHC and SDHD. Heterozygous…
Expand
Highly Cited
2008
Highly Cited
2008
PHD2 mutation and congenital erythrocytosis with paraganglioma.
Charline Ladroue
,
R. Carcenac
,
+7 authors
B. Gardie
New England Journal of Medicine
2008
Corpus ID: 27939883
Prolyl hydroxylase domain (PHD) proteins play a major role in regulating the hypoxia-inducible factor (HIF) that induces…
Expand
Review
2007
Review
2007
The diagnosis and management of malignant phaeochromocytoma and paraganglioma.
A. Chrisoulidou
,
G. Kaltsas
,
I. Ilias
,
A. Grossman
Endocrine-Related Cancer
2007
Corpus ID: 24216815
Malignant phaeochromocytomas are rare tumours accounting for ~10% of all phaeochromocytomas; the prevalence of malignancy among…
Expand
Highly Cited
2005
Highly Cited
2005
Genetic testing in pheochromocytoma or functional paraganglioma.
L. Amar
,
J. Bertherat
,
+17 authors
A. Gimenez-Roqueplo
Journal of Clinical Oncology
2005
Corpus ID: 44995898
PURPOSE To assess the yield and the clinical value of systematic screening of susceptibility genes for patients with…
Expand
Highly Cited
2004
Highly Cited
2004
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
H. Neumann
,
Christian Pawlu
,
+13 authors
C. Eng
Journal of the American Medical Association (JAMA…
2004
Corpus ID: 21673619
CONTEXT Germline mutations of the genes encoding succinate dehydrogenase subunits B (SDHB) and D (SDHD) predispose to…
Expand
Highly Cited
2001
Highly Cited
2001
Benign paragangliomas: clinical presentation and treatment outcomes in 236 patients.
D. Erickson
,
Y. Kudva
,
+4 authors
W. Young
Journal of Clinical Endocrinology and Metabolism
2001
Corpus ID: 21139628
Paragangliomas are rare tumors that arise from extraadrenal chromaffin cells. We examined the clinical characteristics, location…
Expand
Highly Cited
2000
Highly Cited
2000
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
S. Niemann
,
U. Müller
Nature Genetics
2000
Corpus ID: 22747929
Nonchromaffin paragangliomas (PGLs) are usually benign, neural-crest–derived, slow-growing tumours of parasympathetic ganglia…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE