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English
Evaluation of the adolescent or adult with some features of Marfan syndrome
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
title
Evaluation of the adolescent or adult with some features of Marfan syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
main subject
Marfan syndrome
1 reference
based on heuristic
inferred from title
author name string
Reed E Pyeritz
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
American College of Medical Genetics and Genomics
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
publication date
5 January 2012
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
published in
Genetics in Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
volume
14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
page(s)
171-177
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
cites work
Revised diagnostic criteria for the Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The revised Ghent nosology for the Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
International nosology of heritable disorders of connective tissue, Berlin, 1986
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two-dimensional echocardiographic aortic root dimensions in normal children and adults
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aneurysm syndromes caused by mutations in the TGF-beta receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abdominal visceral findings in patients with Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recent progress towards a molecular understanding of Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Medical management of Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rationale and design of a randomized clinical trial of beta-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Articular mobility in an African population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Idiopathic scoliosis: cracking the genetic code and what does it mean?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of aortic root dilation in the Ehlers-Danlos syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FGIM.2011.48
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/GIM.2011.48
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
PubMed publication ID
22237449
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22237449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22237449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 May 2020
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