Results 161 to 170 of about 2,905 (217)

PKHD1-Mutationsspektrum bei pädiatrisch betreuten Patienten mit autosomal-rezessiver polyzystischer Nierenerkrankung (ARPKD)

, 2006
Marc Küpper
openalex   +1 more source

Diagnostic Value of Serum Periostin for Cyst Involution in Children with Multicystic Dysplastic Kidney. [PDF]

J Clin Med
Szmigielska A, Kotuła I, Demkow U, Szmigielska MA, Tutka A.   +4 more
europepmc   +1 more source

[Autosomal recessive polycystic kidney disease in a girl]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Xu XY, Zhou QM, Tian YF, Zhao Q, Pan H, Chen QT, Luo YM, Guo ZZ, Li TH, Yang JH.   +9 more
europepmc   +1 more source

Editorial: Functional study of novel VUS (variant of uncertain significance) mutations in single-gene inherited disease. [PDF]

Front Genet
Yang G, Zhong H, Wen H, Shen Y.
europepmc   +1 more source

Rare Combination of Phenotypes of Karyomegalic Interstitial Nephritis and Autosomal Recessive Polycystic Kidney Disease in an Omani Child. [PDF]

Oman Med J
Al Alawi I, Al Shehhi M, Al Riyami MS, Al Kalbani N, Al Hosni A, Al Mimani A, Al Salmi I, Sayer JA.   +7 more
europepmc   +1 more source

Decoding Liver Fibrosis: How Omics Technologies and Innovative Modeling Can Guide Precision Medicine. [PDF]

Int J Mol Sci
Codotto G, Blarasin B, Tiribelli C, Bellarosa C, Licastro D.   +4 more
europepmc   +1 more source

Genetic diagnosis and prenatal diagnosis of patients with cystic kidney disease in Southwest China. [PDF]

BMC Nephrol
Zhou C, Xiao Y, Xie H, Wei X, Wang J.
europepmc   +1 more source

Ciliary Ion Channels in Polycystic Kidney Disease. [PDF]

Cells
Alshriem LA, Buqaileh R, Alorjani Q, AbouAlaiwi W.   +3 more
europepmc   +1 more source

Enhanced ERK1/2 activity, a central feature of cystogenesis in ARPKD : implications for ion transport phenotype.

, 2005
I. Elias Veizis
openalex   +1 more source