Results 181 to 190 of about 23,590 (248)

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

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

[Nephrogenic diabetes insipidus].

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

duplication syndrome in a Chinese family [PDF]

core   +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

Urine concentration impairment in sickle cell anemia: genuine nephrogenic diabetes insipidus or osmotic diuresis?

Am J Physiol Renal Physiol
de Berny Q, Saint-Jacques C, Santin A, Mattioni S, Steichen O, Chieze R, Frochot V, Letavernier E, Lionnet F, Haymann JP.   +9 more
europepmc   +1 more source