Recurrent autosomal-dominant focal segmental glomerulosclerosis [7]

Kidney International

Volumn 70, Issue 9, 2006, Pages 1664-1665

  Sanna Cherchi, S ^a,b   Somenzi, D ^b   Carnevali, M L ^b   Pilato, F P ^b   Carraro, M ^c   Ghiggeri, G M ^d   Allegri, L ^b  

^a Columbia University College of Physicians and Surgeons ^*  (United States)

^b UNIVERSITY OF PARMA   (Italy)

^c UNIVERSITY OF TRIESTE   (Italy)

^d G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN 1 RECEPTOR ANTAGONIST; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; IMMUNOSUPPRESSIVE AGENT; PODOCIN;

AUTOSOMAL DOMINANT DISORDER; CADAVER KIDNEY; COMORBIDITY; DISEASE ASSOCIATION; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; GLOMERULUS FILTRATION RATE; GRAFT FAILURE; HUMAN; KIDNEY BIOPSY; KIDNEY GRAFT; KIDNEY GRAFT REJECTION; LETTER; NEPHROTIC SYNDROME; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; RECURRENT DISEASE; THERAPY EFFECT; TREATMENT RESPONSE;

ADULT; FEMALE; GLOMERULAR FILTRATION RATE; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; KIDNEY TRANSPLANTATION; MALE; PEDIGREE; RECURRENCE;

EID: 33750202048     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/sj.ki.5001796     Document Type: Letter

References (4)

1. Vincenti F, Ghiggeri GM. New insights into the pathogenesis and the therapy of recurrent focal glomerulosclerosis. Am J Transplant 2005; 5: 1179-1185.
2. Kaplan JM, Kim SH, North KN et al. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nat Genet 2000; 24: 251-256.
3. Winn MP, Conlon PJ, Lynn KL et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 2005; 308: 1801-1804.
4. Conlon PJ, Lynn K, Winn MP et al. Spectrum of disease in familial focal and segmental glomerulosclerosis. Kidney Int 1999; 56: 1863-1871.