X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (40) 40
index medicus (35) 35
paraganglioma - genetics (23) 23
male (21) 21
pheochromocytoma - genetics (21) 21
adult (20) 20
female (20) 20
endocrinology & metabolism (19) 19
middle aged (18) 18
pheochromocytoma (18) 18
adrenal gland neoplasms - genetics (17) 17
germ-line mutation (15) 15
mutation (15) 15
paraganglioma (15) 15
succinate dehydrogenase - genetics (15) 15
life sciences (14) 14
cancer (13) 13
genetic predisposition to disease (11) 11
adolescent (10) 10
succinate-dehydrogenase (10) 10
tumors (10) 10
dna mutational analysis (9) 9
mutations (9) 9
abridged index medicus (8) 8
aged (8) 8
expression (8) 8
genetics & heredity (8) 8
human health and pathology (8) 8
immunohistochemistry (8) 8
oncology (8) 8
child (7) 7
genetic testing (7) 7
genotype (7) 7
germline mutations (7) 7
loss of heterozygosity (7) 7
malignant pheochromocytomas (7) 7
mutation - genetics (7) 7
paraganglioma - pathology (7) 7
adrenal gland neoplasms - pathology (6) 6
gene-mutations (6) 6
genetics (6) 6
membrane proteins - genetics (6) 6
pheochromocytoma - pathology (6) 6
sdhb gene (6) 6
susceptibility (6) 6
aged, 80 and over (5) 5
biochemistry & molecular biology (5) 5
cohort studies (5) 5
genes (5) 5
genetic aspects (5) 5
genomes (5) 5
young adult (5) 5
[sdv]life sciences [q-bio] (4) 4
diagnosis (4) 4
gene (4) 4
gene expression profiling (4) 4
gene mutations (4) 4
hereditary paraganglioma (4) 4
hypertension (4) 4
hypoxia (4) 4
identification (4) 4
phenotype (4) 4
point mutation (4) 4
sdhb (4) 4
succinate dehydrogenase - metabolism (4) 4
tumor-suppressor gene (4) 4
vhl protein (4) 4
von hippel-lindau tumor suppressor protein - genetics (4) 4
[sdv.can]life sciences [q-bio]/cancer (3) 3
[sdv.mhep]life sciences [q-bio]/human health and pathology (3) 3
adrenal gland neoplasms - diagnosis (3) 3
age factors (3) 3
analysis (3) 3
benign (3) 3
complex ii (3) 3
complex-ii (3) 3
electron transport complex ii - genetics (3) 3
endocrine system diseases (3) 3
endocrinology and metabolism (3) 3
france (3) 3
gene expression (3) 3
gene expression regulation, neoplastic (3) 3
genetic screening (3) 3
genomics (3) 3
head and neck neoplasms - genetics (3) 3
hereditary (3) 3
heterozygote (3) 3
loss of heterozygosity - genetics (3) 3
mitochondria (3) 3
mitochondria - metabolism (3) 3
neoplasms (3) 3
neovascularization, pathologic - genetics (3) 3
oligonucleotide array sequence analysis (3) 3
paraganglioma - diagnosis (3) 3
paraganglioma - enzymology (3) 3
paraganglioma - metabolism (3) 3
patient (3) 3
pedigree (3) 3
pheochromocytoma - diagnosis (3) 3
pheochromocytoma - metabolism (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Reviews Endocrinology, ISSN 1759-5029, 04/2017, Volume 13, Issue 4, pp. 233 - 247
Journal Article
Journal Article
CANCER RESEARCH, ISSN 0008-5472, 04/2018, Volume 78, Issue 8, pp. 1914 - 1922
Comprehensive genetic analyses have identified germline SDHB and FH gene mutations as predominant causes of metastatic paraganglioma and pheochromocytoma.... 
ONCOLOGY | PHEOCHROMOCYTOMAS | PROTEINS | CRISPR | Pheochromocytoma | Paraganglioma | Metastasis | Metastases | Heterozygosity | Carriers | Mitochondria | Malate | Loss of heterozygosity | Genetic analysis | Mutation | a-Ketoglutaric acid | Cancer | Tumors
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2009, Volume 4, Issue 9, p. e7094
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 03/2017, Volume 86, Issue 3, pp. 332 - 339
Journal Article
Cancer Cell, ISSN 1535-6108, 06/2013, Volume 23, Issue 6, pp. 739 - 752
Journal Article
Current Opinion in Oncology, ISSN 1040-8746, 01/2016, Volume 28, Issue 1, pp. 5 - 10
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 08/2010, Volume 19, Issue 15, pp. 3011 - 3020
Journal Article
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, ISSN 0893-3952, 08/2019
The development of pheochromocytomas and paragangliomas is strongly linked to the presence of germline mutations in more than 15 predisposing genes. Among... 
Journal Article