Autor
|
-
Adwani SS, Whitehead BF, Rees PG, et al.
(es)
-
Gonzalez IL
(es)
-
Kirwin SM, Vinette KM, Schwartz SB, Funanage VL, Gonzalez IL
(es)
-
Kuijpers TW, Maianski NA, Tool AT, et al.
(es)
-
Mangat J, Lunnon-Wood T, Rees P, Elliott M, Burch M
(es)
-
Mazzocco MM, Henry AE, Kelly RI
(es)
-
Orstavik KH, Orstavik RE, Naumova AK, et al.
(es)
-
Spencer CT, Byrne BJ, Gewitz MH, et al.
(es)
-
Yen TY, Hwu WL, Chien YH, et al.
(es)
|
Año
|
-
1997
(xsd:integer)
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1998
(xsd:integer)
-
2004
(xsd:integer)
-
2005
(xsd:integer)
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2007
(xsd:integer)
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2008
(xsd:integer)
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rdfs:comment
|
-
El síndrome de Barth (BTHS), también conocido como aciduria 3-metilglutaconio tipo II, es un extraño y a la vez serio desorden genético.
(es)
|
foaf:depiction
|
|
Diseases DB
|
|
dbpedia-owl:diseasesdb
|
|
Doi
|
-
101002
(xsd:integer)
-
101007
(xsd:integer)
-
101016
(xsd:integer)
-
101086
(xsd:integer)
-
101097
(xsd:integer)
-
101111
(xsd:integer)
-
101182
(xsd:integer)
|
Imagen
|
|
foaf:isPrimaryTopicOf
|
|
Issue
|
-
1
(xsd:integer)
-
10
(xsd:integer)
-
2
(xsd:integer)
-
3
(xsd:integer)
-
4
(xsd:integer)
-
5
(xsd:integer)
-
8
(xsd:integer)
|
rdfs:label
|
|
Mes
|
-
abril
(es)
-
agosto
(es)
-
febrero
(es)
-
mayo
(es)
-
noviembre
(es)
|
foaf:name
|
|
Nombre
|
|
dbpedia-owl:omim
|
|
OMIM
|
|
Orphanet Number
|
|
Pie
|
|
Pmc
|
|
Pmid
|
-
14764526
(xsd:integer)
-
15793838
(xsd:integer)
-
16235007
(xsd:integer)
-
17241629
(xsd:integer)
-
17353728
(xsd:integer)
-
17430492
(xsd:integer)
-
17846786
(xsd:integer)
-
9049131
(xsd:integer)
-
9792874
(xsd:integer)
|
Is
foaf:primaryTopic
of
|
|
Publicación
|
-
American Journal of Human Genetics
(es)
-
American Journal of Medical Genetics. Part a
(es)
-
Blood
(es)
-
European Journal of Pediatrics
(es)
-
Fertility and Sterility
(es)
-
Journal of Developmental and Behavioral Pediatrics: JDBP
(es)
-
Pediatric Cardiology
(es)
-
Pediatric Transplantation
(es)
|
Páginas
|
-
143
(xsd:integer)
-
1457
(xsd:integer)
-
22
(xsd:integer)
-
327
(xsd:integer)
-
3915
(xsd:integer)
-
409
(xsd:integer)
-
632
(xsd:integer)
-
941
(xsd:integer)
-
976
(xsd:integer)
|
dcterms:subject
|
|
dbpedia-owl:thumbnail
|
|
rdf:type
|
|
Título
|
-
Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review
(es)
-
Barth syndrome is associated with a cognitive phenotype
(es)
-
Barth syndrome: TAZ gene mutations, mRNAs, and evolution
(es)
-
Heart transplantation for Barth syndrome
(es)
-
Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation
(es)
-
Neutrophils in Barth syndrome avidly bind annexin-V in the absence of apoptosis
(es)
-
Successful cardiac transplantation in Barth syndrome--single-centre experience of four patients
(es)
-
Ventricular arrhythmia in the X-linked cardiomyopathy Barth syndrome
(es)
-
X chromosome inactivation in carriers of Barth syndrome
(es)
|
Volumen
|
-
103
(xsd:integer)
-
11
(xsd:integer)
-
134
(xsd:integer)
-
167
(xsd:integer)
-
18
(xsd:integer)
-
26
(xsd:integer)
-
28
(xsd:integer)
-
63
(xsd:integer)
-
87
(xsd:integer)
|
prov:wasDerivedFrom
|
|
Is
dbpedia-owl:wikiPageDisambiguates
of
|
|
dbpedia-owl:wikiPageExternalLink
|
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dbpedia-owl:wikiPageID
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dbpedia-owl:wikiPageLength
|
|
dbpedia-owl:wikiPageOutDegree
|
|
Is
dbpedia-owl:wikiPageRedirects
of
|
|
dbpedia-owl:wikiPageRevisionID
|
|
prop-latam:wikiPageUsesTemplate
|
|
dbpedia-owl:wikiPageWikiLink
|
[12 values]
|
Is
dbpedia-owl:wikiPageWikiLink
of
|
|