Results 101 to 110 of about 3,546 (164)

The First Case of Congenital Nephrogenic Diabetes Insipidus Caused by AVPR2 Disruption Because of 4q25 Insertional Translocation. [PDF]

Ann Lab Med
Kim B, Ahn YH, Park JH, Lim HS, Chae SW, Lee JS, Kang HG, Kim MJ, Seong MW.   +8 more
europepmc   +1 more source

A case of ifosfamide-induced acute kidney injury, Fanconi syndrome, and nephrogenic diabetes insipidus. [PDF]

CEN Case Rep
Hoang S, Pujar T, Bellorin-Font E, Edwards JC, Miyata KN.   +4 more
europepmc   +1 more source

The β3-AR agonist BRL37344 ameliorates the main symptoms of X-linked nephrogenic diabetes insipidus in the mouse model of the disease. [PDF]

J Cell Mol Med
Milano S, Saponara I, Gerbino A, Carmosino M, Svelto M, Procino G.   +5 more
europepmc   +1 more source

Targeted long-read sequencing identified a causal structural variant in X-linked nephrogenic diabetes insipidus. [PDF]

BMC Med Genomics
Strych L, Černá M, Hejnalová M, Zavoral T, Komrsková P, Tejcová J, Bitar I, Sládková E, Sýkora J, Šubrt I.   +9 more
europepmc   +1 more source

[Nephrogenic diabetes insipidus].

Pediatria polska, 1972
A, Radzikowski, T, Zalewski, A, Milanowski   +2 more
openaire   +3 more sources

A Rare Case of Congenital Nephrogenic Diabetes Insipidus Associated with Aquaporin 2 Gene Mutation and Subsequent Acute Lymphoblastic Leukemia: Impact of Steroids on Kidney Function. [PDF]

Am J Case Rep
Al-Thiabat H, Abu-Aqoulah A, Kanaan D, Matalka MI, Al-Sweedan S.   +4 more
europepmc   +1 more source

Retracted: A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation. [PDF]

Biomed Res Int
International BR.
europepmc   +1 more source