Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis

Journal of the American Society of Nephrology

Volumn 12, Issue 12, 2001, Pages 2742-2746

  Caridi, G ^a   Bertelli, R ^a   Carrea, A ^a   Di Duca, M ^a   Catarsi, P ^a   Artero, M ^a   Carraro, M ^a   Zennaro, C ^a   Candiano, G ^a   Musante, L ^a   Seri, M ^a   Ginevri, F ^a   Perfumo, F ^a   Ghiggeri, G M ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHOSPHAMIDE; CYCLOSPORIN A; GENE PRODUCT; IMMUNOSUPPRESSIVE AGENT; PODOCIN; STEROID; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DINUCLEOTIDE REPEAT; EXON; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; GLOMERULOSCLEROSIS; HAPLOTYPE; HETEROZYGOSITY; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; KIDNEY FAILURE; KIDNEY FUNCTION; KIDNEY GRAFT; MALE; NEPHROTIC SYNDROME; ONSET AGE; PHENOTYPE; PLASMAPHERESIS; PREVALENCE; PRIORITY JOURNAL; PROTEINURIA; RECURRENT DISEASE; REMISSION; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 0035199469     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
2. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
3. Getting a foothold in nephrotic syndrome
4. Congenital nephrotic syndromes
5. Positionally cloned gene for a novel glomerular protein-nephrin-is mutated in congenital nephrotic syndrome
6. Congenital nephrotic syndrome in mice lacking CD2-associated protein
7. Incidence, treatment, and outcome of recurrent focal segmental glomerulosclerosis posttransplantation in 42 allografts in children-a single-center experience
8. Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children
9. Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis
10. A novel polymorphism (c288C>T) of the NPHS2 gene identified in a Taiwan Chinese family
11. Familial steroid-resistant nephrotic syndromes: Recent advances
12. Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis