Phenotypic expansion of DGKE-associated diseases

Journal of the American Society of Nephrology

Volumn 25, Issue 7, 2014, Pages 1408-1414

  Westland, Rik ^a,b   Bodria, Monica ^c,d   Carrea, Alba ^c   Lata, Sneh ^a   Scolari, Francesco ^e   Fremeaux Bacchi, Veronique ^f,g   D'Agati, Vivette D ^h   Lifton, Richard P ⁱ   Gharavi, Ali G ^a   Marco Ghiggeri, Gian ^c   Sanna Cherchi, Simone ^a  

^a Department of Neurology and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain   (United States)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^c G GASLINI INSTITUTE   (Italy)

^d UNIVERSITY OF PARMA   (Italy)

^e UNIVERSITY OF BRESCIA   (Italy)

^f HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^g CENTRE DE RECHERCHE DES CORDELIERS   (France)

^h Howard Hughes Medical Institute   (United States)

ⁱ YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN RECEPTOR ANTAGONIST; COMPLEMENT COMPONENT C3; DIACYLGLYCEROL KINASE; DIACYLGLYCEROL KINASE EPSILON; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; HAPTOGLOBIN; LACTATE DEHYDROGENASE; UNCLASSIFIED DRUG; DIACYLGLYCEROL KINASE EPSILON, HUMAN;

ACUTE KIDNEY FAILURE; ARTICLE; CASE REPORT; CHILD; COMPLEMENT ACTIVATION; COMPLEMENT BLOOD LEVEL; DISEASE ASSOCIATION; EXOME; FEMALE; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; HEMATURIA; HEMOLYSIS; HEMOLYTIC UREMIC SYNDROME; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; KIDNEY BIOPSY; LACTATE DEHYDROGENASE BLOOD LEVEL; MALE; PHENOTYPE; PLASMA TRANSFUSION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEINURIA; SINGLE NUCLEOTIDE POLYMORPHISM; THROMBOTIC THROMBOCYTOPENIC PURPURA; VIRUS INFECTION; GENETICS; PEDIGREE;

CHILD, PRESCHOOL; DIACYLGLYCEROL KINASE; FEMALE; HEMOLYTIC-UREMIC SYNDROME; HUMANS; MALE; PEDIGREE; PHENOTYPE;

EID: 84902135216     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2013080886     Document Type: Article

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