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English
The genetic basis of pheochromocytoma: who to screen and how?
scientific article published on 01 February 2006
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
title
The genetic basis of pheochromocytoma: who to screen and how?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
main subject
phaeochromocytoma
1 reference
based on heuristic
inferred from title
author
Anne-Paule Gimenez-Roqueplo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Pierre-François Plouin
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
publication date
1 February 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Nature Clinical Practice Endocrinology and Metabolism
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
60-61
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
cites work
Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
21 January 2018
von Hippel-Lindau disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the association of succinate dehydrogenase mutations with hereditary paraganglioma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ-line mutations in nonsyndromic pheochromocytoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic testing in pheochromocytoma or functional paraganglioma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Controversies and ethical issues in cancer-genetics clinics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNCPENDMET0097
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NCPENDMET0097
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed ID
16932255
1 reference
stated in
Europe PubMed Central
PubMed ID
16932255
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932255%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
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