Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood

Journal of the American Society of Nephrology

Volumn 12, Issue 2, 2001, Pages 374-378

  Fuchshuber, A ^a   Gribouval, O ^a   Ronner, V ^a   Kroiss, S ^a   Karle, S ^a   Brandis, M ^a   Hildebrandt, F ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID;

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CHILDHOOD DISEASE; CHROMOSOME 1; CLINICAL ARTICLE; DISEASE CLASSIFICATION; DISEASE COURSE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; KIDNEY BIOPSY; MALE; NEPHROTIC SYNDROME; ONSET AGE; PRIORITY JOURNAL; STEROID RESPONSIVE IDIOPATHIC NEPHROTIC SYNDROME; STEROID THERAPY;

EID: 0035141496     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: 10.1681/asn.v122374     Document Type: Article

References (20)

1. Familial nephrotic syndrome with focal glomerular sclerosis
2. Familial nephrotic syndrome and focal segmental glomerulosclerosis
3. The familial occurrence of focal segmental glomerular sclerosis
4. Familial nephrotic syndrome
5. The familial nephrotic syndrome: I. A European survey
6. The familial nephrotic syndrome: II. A clinicopathological study
7. Familial focal segmental glomerulosclerosis
8. Antignac C: Mapping a gene (SRN1) to chromosome 1q25-q 31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
9. Antignac C: NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
10. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13
11. Mutations in ACTN4, encoding alpha-actinin- 4, cause familial focal segmental glomerulosclerosis
12. Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity
13. Arbeitsgemeinschaft fur Pädiatrische Nephrologie: Short versus standard prednisone therapy for initial treatment of idiopathic nephrotic syndrome in children
14. Primary nephrotic syndrome in children: Clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children
15. The use of plasma creatinine concentration for estimating glomerular filtration rate in infants, children, and adolescents
16. A comprehensive genetic map of the human genome based on 5,264 microsatellites
17. Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)
18. Strategies for multilocus linkage analysis in humans
19. A new method for sequencing DNA
20. Prognostic significance of the early course of minimal change nephrotic syndrome: Report of the International Study of Kidney Disease in Children