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Volumn 85, Issue 6, 2014, Pages 1477-1478
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The Case Renal dysfunction in a pregnant patient with IgA nephropathy
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Author keywords
[No Author keywords available]
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Indexed keywords
ASPARTIC ACID;
CREATININE;
HAPTOGLOBIN;
LACTATE DEHYDROGENASE;
THROMBOMODULIN;
TYROSINE;
THBD PROTEIN, HUMAN;
ADULT;
AMINO ACID SUBSTITUTION;
ANEMIA;
CASE REPORT;
COMPLEMENT ALTERNATIVE PATHWAY;
CREATININE BLOOD LEVEL;
DIFFERENTIAL DIAGNOSIS;
FEMALE;
HEADACHE;
HELLP SYNDROME;
HEMATURIA;
HEMODIALYSIS;
HEMOLYTIC UREMIC SYNDROME;
HETEROZYGOTE;
HUMAN;
HUMAN TISSUE;
IMMUNOGLOBULIN A NEPHROPATHY;
IMMUNOGLOBULIN DEPOSITION;
KIDNEY BIOPSY;
KIDNEY FAILURE;
KIDNEY TRANSPLANTATION;
LIVING DONOR;
MISSENSE MUTATION;
NOTE;
NUCLEIC ACID BASE SUBSTITUTION;
PREGNANT WOMAN;
PRIORITY JOURNAL;
THROMBOCYTOPENIA;
THROMBOMODULIN GENE;
THROMBOTIC THROMBOCYTOPENIC PURPURA;
VAGINAL DELIVERY;
YOUNG ADULT;
ADOLESCENT;
ATYPICAL HEMOLYTIC UREMIC SYNDROME;
BIOPSY;
COMPLICATION;
FLUORESCENT ANTIBODY TECHNIQUE;
GENETIC PREDISPOSITION;
GENETICS;
GLOMERULONEPHRITIS, IGA;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
PREGNANCY;
PREGNANCY COMPLICATIONS;
RENAL INSUFFICIENCY;
RENAL REPLACEMENT THERAPY;
TREATMENT OUTCOME;
ADOLESCENT;
ATYPICAL HEMOLYTIC UREMIC SYNDROME;
BIOPSY;
DNA MUTATIONAL ANALYSIS;
FEMALE;
FLUORESCENT ANTIBODY TECHNIQUE;
GENETIC PREDISPOSITION TO DISEASE;
GLOMERULONEPHRITIS, IGA;
HUMANS;
KIDNEY TRANSPLANTATION;
MUTATION, MISSENSE;
PHENOTYPE;
PREGNANCY;
PREGNANCY COMPLICATIONS;
RENAL DIALYSIS;
RENAL INSUFFICIENCY;
THROMBOMODULIN;
TREATMENT OUTCOME;
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EID: 84901844363
PISSN: 00852538
EISSN: 15231755
Source Type: Journal
DOI: 10.1038/ki.2013.322 Document Type: Article |
Times cited : (4)
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References (5)
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