Broadening the spectrum of diseases related to podocin mutations

Journal of the American Society of Nephrology

Volumn 14, Issue 5, 2003, Pages 1278-1286

  Caridi, Gianluca ^a   Bertelli, Roberta ^a   Di Duca, Marco ^a   Dagnino, Monica ^a   Emma, Francesco ^b   Muda, Andrea Onetti ^c   Scolari, Francesco ^d   Miglietti, Nunzia ^e   Mazzucco, Gianna ^f   Murer, Luisa ^g   Carrea, Alba ^a   Massella, Laura ^b   Rizzoni, Gianfranco ^b   Perfumo, Francesco ^a   Ghiggeri, Gian Marco ^a  

^a G GASLINI INSTITUTE   (Italy)

^b Section of Nephrology   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d SPEDALI CIVILI   (Italy)

^e UNIVERSITY OF BRESCIA   (Italy)

^f UNIVERSITY OF TURIN   (Italy)

^g UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENTARY DNA; CYCLOPHOSPHAMIDE; CYCLOSPORIN; METHYLPREDNISOLONE; MUTANT PROTEIN; NEPHRIN; PODOCIN; PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CHILD; CLINICAL FEATURE; COMPLEMENT DEPOSITION; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENE FREQUENCY; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; IMMUNOHISTOCHEMISTRY; INFANT; MAJOR CLINICAL STUDY; MALE; NEPHROTIC SYNDROME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEINURIA; SIBLING; STEROID THERAPY;

EID: 0037407214     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ASN.0000060578.79050.E0     Document Type: Article

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