DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
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Recessive mutations in DGKE cause atypical hemolytic-uremic syndromeCurrent treatment of atypical hemolytic uremic syndromeDiacylglycerol Kinase-ε: Properties and Biological RolesGuidelines on the Use of Therapeutic Apheresis in Clinical Practice-Evidence-Based Approach from the Writing Committee of the American Society for Apheresis: The Seventh Special Issue.Genetic testing in steroid-resistant nephrotic syndrome: when and how?DGKE and atypical HUS.Complement therapy in atypical haemolytic uraemic syndrome (aHUS).How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndromePhenotypic expansion of DGKE-associated diseases[Pathophysiology of atypical hemolytic uremic syndrome. Ten years of progress, from laboratory to patient].Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome.Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids.Podocyte dysfunction in atypical haemolytic uraemic syndrome.Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic SyndromeLoss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production.Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.Exploring the genetic basis of early-onset chronic kidney disease.Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patientsThe Genetics of Nephrotic Syndrome.Making sense of the spectrum of glomerular disease associated with complement dysregulation.The glomerulus: the sphere of influence.The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overview.Whole exome sequencing: a state-of-the-art approach for defining (and exploring!) genetic landscapes in pediatric nephrology.The expanding phenotypic spectra of kidney diseases: insights from genetic studies.At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome: A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature.The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.Update on C3 glomerulopathy.Genomics in the renal clinic - translating nephrogenetics for clinical practiceDGKE disruption ditches complement and drives p38 signaling.Complement C5-inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea.Diacylglycerol Kinase alpha is Involved in the Vitamin E-Induced Amelioration of Diabetic Nephropathy in Mice.Factors influencing treatment of atypical hemolytic uremic syndrome.Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Towards precision nephrology: the opportunities and challenges of genomic medicine.Diseases of complement dysregulation-an overview.Thrombotic Microangiopathy and the Kidney.C3 glomerulonephritis and autoimmune disease: more than a fortuitous association?Monogenic Causes of Proteinuria in Children.C3 glomerulonephritis and thrombotic microangiopathy of renal allograft after pulmonary infection in a male with concomitant two complement factor I gene variations: a case report.
P2860
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P2860
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
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2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@ast
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@en
type
label
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@ast
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@en
prefLabel
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@ast
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@en
P2093
P2860
P356
P1476
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
@en
P2093
Ali Duzova
Alysha Rauhauser
Aysin Bakkaloglu
Benjamin Wakeland
Binghua Li
Chandra Mohan
Chaoying Liang
Chou-Long Huang
Deborah Lewis
Dongmei Lu
P2860
P304
P356
10.1681/ASN.2012090903
P577
2012-12-28T00:00:00Z