PubMed Clinical Queries
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Results for Clinical Studies: Therapy/Broad
5 of 5 results sorted by: Most RecentSee all results in PubMed (5)
Ask-Upmark kidney in a girl with neurofibromatosis type 1.
CEN Case Rep. 2020. PMID: 32277359 Free PMC article.
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
Pediatr Nephrol. 2019. PMID: 31001663 Free PMC article.
Successful ABO-incompatible living-donor renal transplant without splenectomy for renal coloboma syndrome: a case report.
Exp Clin Transplant. 2014. PMID: 23902562 Free article.
Papillorenal syndrome after Beta-interferon treatment in pregnancy.
Ren Fail. 2009. PMID: 19839859
Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice.
Hum Mol Genet. 2000. PMID: 10587573