Results 181 to 190 of about 8,417 (217)

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

αENaC-Mediated Lithium Absorption Promotes Nephrogenic Diabetes Insipidus

, 2010
Birgitte Mønster Christensen, Annie Mercier Zuber, Johannes Loffing, Jean‐Christophe Stehle, Peter M.T. Deen, Bernard C. Rossier, Edith Hümmler   +6 more
openalex   +2 more sources

Nephrogenic diabetes insipidus in mice lacking aquaporin-3 water channels

, 2000
Tonghui Ma, Yuanlin Song, Baoxue Yang, Anne-Marie Gillespie, Elaine J. Carlson, Charles J. Epstein, A. S. Verkman   +6 more
openalex   +2 more sources

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

duplication syndrome in a Chinese family [PDF]

core   +1 more source