15754282

Source:http://linkedlifedata.com/resource/pubmed/id/15754282

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0012634, umls-concept:C0026882, umls-concept:C0056207, umls-concept:C0155765, umls-concept:C1314792, umls-concept:C1826260
pubmed:issue	3
pubmed:dateCreated	2005-3-8
pubmed:abstractText	cblC disease is a cause of hemolytic uremic syndrome (HUS), which has been primarily described in neonates and infants with severe renal and neurological lesions.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8110075
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Betaine, http://linkedlifedata.com/resource/pubmed/chemical/CBLC protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Complement Factor H, http://linkedlifedata.com/resource/pubmed/chemical/Folic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Haptoglobins, http://linkedlifedata.com/resource/pubmed/chemical/Hydroxocobalamin, http://linkedlifedata.com/resource/pubmed/chemical/Methylenetetrahydrofolate..., http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-cbl, http://linkedlifedata.com/resource/pubmed/chemical/Vitamin B 12, http://linkedlifedata.com/resource/pubmed/chemical/complement factor H, human
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1523-6838
pubmed:author	pubmed-author:BorderieDidierD, pubmed-author:DeschênesGeorgesG, pubmed-author:FavierRémiR, pubmed-author:Frémeaux-BacchiVéroniqueV, pubmed-author:GiraudierStéphaneS, pubmed-author:GuigonisVincentV, pubmed-author:MassyZiadZ, pubmed-author:MougenotBéatriceB, pubmed-author:RosenblattDavid SDS
pubmed:issnType	Electronic
pubmed:volume	45
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	588-95
pubmed:dateRevised	2005-11-17
pubmed:meshHeading	pubmed-meshheading:15754282-Anemia, pubmed-meshheading:15754282-Betaine, pubmed-meshheading:15754282-Child, pubmed-meshheading:15754282-Combined Modality Therapy, pubmed-meshheading:15754282-Complement Factor H, pubmed-meshheading:15754282-Drug Therapy, Combination, pubmed-meshheading:15754282-Endothelium, Vascular, pubmed-meshheading:15754282-Female, pubmed-meshheading:15754282-Folic Acid, pubmed-meshheading:15754282-Genetic Predisposition to Disease, pubmed-meshheading:15754282-Genotype, pubmed-meshheading:15754282-Haptoglobins, pubmed-meshheading:15754282-Hemolytic-Uremic Syndrome, pubmed-meshheading:15754282-Humans, pubmed-meshheading:15754282-Hydroxocobalamin, pubmed-meshheading:15754282-Hypertension, pubmed-meshheading:15754282-Kidney, pubmed-meshheading:15754282-Methylenetetrahydrofolate Reductase (NADPH2), pubmed-meshheading:15754282-Mutation, Missense, pubmed-meshheading:15754282-Nephrotic Syndrome, pubmed-meshheading:15754282-Plasma Exchange, pubmed-meshheading:15754282-Point Mutation, pubmed-meshheading:15754282-Proteinuria, pubmed-meshheading:15754282-Proto-Oncogene Proteins, pubmed-meshheading:15754282-Proto-Oncogene Proteins c-cbl, pubmed-meshheading:15754282-Renal Dialysis, pubmed-meshheading:15754282-Vitamin B 12
pubmed:year	2005
pubmed:articleTitle	Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.
pubmed:affiliation	Department of Pediatric Nephrology, Hôpital Armand-Trousseau, Paris, France.
pubmed:publicationType	Journal Article, Case Reports