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Volumn 9, Issue 10, 2009, Pages 2435-2440
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Potential Donor-recipient MYH9 genotype interactions in posttransplant nephrotic syndrome after pediatric kidney transplantation
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Author keywords
African Americans; Focal segmental glomerulosclerosis; MYH9; Nephrotic syndrome; Pediatric recipient; Renal transplant
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Indexed keywords
ALEMTUZUMAB;
COMPLEMENT COMPONENT C1Q;
COMPLEMENT COMPONENT C3;
CREATINE KINASE;
CREATININE;
HLA A ANTIGEN;
HLA B ANTIGEN;
HLA DR ANTIGEN;
IMMUNOGLOBULIN A;
IMMUNOGLOBULIN G;
IMMUNOGLOBULIN KAPPA CHAIN;
IMMUNOGLOBULIN M;
MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER;
MYH9 E1 PROTEIN;
PREDNISONE;
PROTEIN;
RITUXIMAB;
SERUM ALBUMIN;
STEROID;
TACROLIMUS;
THYMOCYTE ANTIBODY;
UNCLASSIFIED DRUG;
ACUTE DISEASE;
ADOLESCENT;
ADULT;
AFRICAN AMERICAN;
ALBUMIN BLOOD LEVEL;
ALLELE;
ARTICLE;
BALLOON CATHETER;
BLADDER CATHETERIZATION;
BRAIN DEATH;
BRAIN HYPOXIA;
BRAIN INJURY;
CADAVER KIDNEY;
CAPILLARY;
CHILD;
CHRONIC PYELONEPHRITIS;
CREATINE KINASE BLOOD LEVEL;
CREATININE BLOOD LEVEL;
DRUG PULSE THERAPY;
ELECTRON MICROSCOPY;
ENVIRONMENT;
ERYTHROCYTE URINE LEVEL;
EUROPEAN AMERICAN;
FEMALE;
FOCAL GLOMERULOSCLEROSIS;
GENE INTERACTION;
GENETIC RISK;
GENETIC VARIABILITY;
GENOTYPE;
GLOMERULUS;
GRAFT RECIPIENT;
HAPLOTYPE;
HEART VENTRICLE TACHYCARDIA;
HEMODIALYSIS;
HLA SYSTEM;
HUMAN;
HUMAN TISSUE;
HYDRONEPHROSIS;
HYPERTENSION;
HYPOALBUMINEMIA;
IDIOPATHIC DISEASE;
IMMUNE COMPLEX NEPHRITIS;
IMMUNOFLUORESCENCE MICROSCOPY;
IMMUNOSUPPRESSIVE TREATMENT;
INFORMED CONSENT;
INTENSIVE CARE;
KIDNEY BIOPSY;
KIDNEY FAILURE;
KIDNEY GRAFT REJECTION;
KIDNEY INJURY;
KIDNEY TRANSPLANTATION;
KIDNEY TUBULE DAMAGE;
LEUKOCYTE;
MALE;
MENINGOMYELOCELE;
MESANGIUM;
MESANGIUM CELL;
MICROSCOPY;
NEPHRECTOMY;
NEPHROTIC SYNDROME;
NEUROGENIC BLADDER;
PATHOLOGY;
PEDIATRICS;
PLASMAPHERESIS;
POSTOPERATIVE COMPLICATION;
PRIORITY JOURNAL;
PROTEIN URINE LEVEL;
PROTEINURIA;
RECURRENT DISEASE;
RELATIVE DENSITY;
RESUSCITATION;
SCAR FORMATION;
SCHOOL CHILD;
SINGLE NUCLEOTIDE POLYMORPHISM;
SPORTING EVENT;
TREATMENT DURATION;
URINALYSIS;
URINE VOLUME;
ADOLESCENT;
CHILD, PRESCHOOL;
FEMALE;
GENOTYPE;
HAPLOTYPES;
HUMANS;
KIDNEY TRANSPLANTATION;
MALE;
MOLECULAR MOTOR PROTEINS;
MYOSIN HEAVY CHAINS;
NEPHROTIC SYNDROME;
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EID: 70349210726
PISSN: 16006135
EISSN: 16006143
Source Type: Journal
DOI: 10.1111/j.1600-6143.2009.02806.x Document Type: Article |
Times cited : (14)
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References (12)
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