Results 131 to 140 of about 93,897 (194)

Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1. [PDF]

Clin Exp Nephrol, 2021
Inoue T, Nagano C, Matsuo M, Yamamura T, Sakakibara N, Horinouchi T, Shibagaki Y, Ichikawa D, Aoto Y, Ishiko S, Ishimori S, Rossanti R, Iijima K, Nozu K.   +13 more
europepmc   +1 more source

Dent disease manifested as Fanconi syndrome and early onset renal dysfunction: a pedigree report with a literature review

Linchuang shenzangbing zazhi
Li-xia Wang, Li-juan Ma, Hong-wen Zhang
doaj   +1 more source

Phenotype and genotype analyses of 21 Chinese patients with Dent disease. [PDF]

J Biomed Res
Che R, Cai Y, Zhou W, Zhao S, Huang S.
europepmc   +1 more source

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report. [PDF]

Case Rep Nephrol Dial
Del Prete D, Ceol M, Giannella A, Ceolotto G, Sgrò E, Priante G, Fedrigo M, Anglani F, Nalesso F.   +8 more
europepmc   +1 more source

A Focus on the Proximal Tubule Dysfunction in Dent Disease Type 1. [PDF]

Genes (Basel)
de Combiens E, Sakhi IB, Lourdel S.
europepmc   +1 more source

Tubular proteinuria due to hereditary endocytic receptor disorder of the proximal tubule: Dent disease and chronic benign proteinuria. [PDF]

Pediatr Nephrol
Sakakibara N, Nozu K.
europepmc   +1 more source

Bioinformatics analysis of a <i>CLCN5</i> geneframeshift mutation in a patient with Dent disease. [PDF]

Zhong Nan Da Xue Xue Bao Yi Xue Ban
Zhang Y, Li N, Fan L, Liu J.
europepmc   +1 more source

Dent disease type 2 [PDF]

, 2020
openaire   +1 more source

Onset mechanism of a female patient with Dent disease 2

Clinical and Experimental Nephrology, 2020
T. Okamoto, Nana Sakakibara, K. Nozu, Toshiyuki Takahashi, Asako Hayashi, Yasuyuki Sato, C. Nagano, M. Matsuo, K. Iijima, A. Manabe   +9 more
semanticscholar   +1 more source

Dent disease type 1 [PDF]

, 2020
openaire   +1 more source