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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2009-6-4
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pubmed:abstractText |
Mutations in nephrin (NPHS1) and podocin (NPHS2) genes represent a major cause of idiopathic nephrotic syndrome (NS) in children. It is not yet clear whether the presence of a single mutation acts as a modifier of the clinical course of NS.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-10700177,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-10742096,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-11317351,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-11729243,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-12047969,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-12464671,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-12495287,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-12707396,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-14871423,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-14978175,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-15086927,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-15253708,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-15496146,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-15531003,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-16439601,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-16481888,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-16900088,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-16909243,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-17942957,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-18216321,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-18462046,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-18823551,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-4137139,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-7334749,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-9505282,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-9660941,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19406966-9915943
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1555-905X
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pubmed:author |
pubmed-author:AllegriLandinoL,
pubmed-author:AmoreAlessandroA,
pubmed-author:BarbanoGiancarloG,
pubmed-author:CaridiGianlucaG,
pubmed-author:CoppoRosannaR,
pubmed-author:DagninoMonicaM,
pubmed-author:De PaloTommasoT,
pubmed-author:EdefontiAlbertoA,
pubmed-author:EmmaFrancescoF,
pubmed-author:GesualdoLoretoL,
pubmed-author:GhiggeriGian MarcoGM,
pubmed-author:GiganteMaddalenaM,
pubmed-author:MurerLuisaL,
pubmed-author:MurtasCorradoC,
pubmed-author:PenzaRosaR,
pubmed-author:RavaniPietroP,
pubmed-author:ScolariFrancescoF,
pubmed-author:TrivelliAntonellaA
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pubmed:issnType |
Electronic
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1065-72
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:19406966-Adolescent,
pubmed-meshheading:19406966-Child,
pubmed-meshheading:19406966-Child, Preschool,
pubmed-meshheading:19406966-Female,
pubmed-meshheading:19406966-Follow-Up Studies,
pubmed-meshheading:19406966-Genetic Variation,
pubmed-meshheading:19406966-Heterozygote,
pubmed-meshheading:19406966-Humans,
pubmed-meshheading:19406966-Infant,
pubmed-meshheading:19406966-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:19406966-Kaplan-Meier Estimate,
pubmed-meshheading:19406966-Male,
pubmed-meshheading:19406966-Membrane Proteins,
pubmed-meshheading:19406966-Nephrotic Syndrome,
pubmed-meshheading:19406966-Point Mutation
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pubmed:year |
2009
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pubmed:articleTitle |
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.
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pubmed:affiliation |
Division of Nephrology and Laboratory on Pathophysiology of Uremia Istituto Giannina Gaslini, Genova, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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