Results 71 to 80 of about 4,888 (207)

Idiopathic hypergammaglobulinaemia associated with nephrogenic diabetes insipidus and distal renal tubular acidosis [PDF]

, 1984
Barbara A. Spruce, P. H. Baylis, David Kerr, A R Morley   +3 more
openalex   +1 more source

Novel AQP2 Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus

, 2021
Qian Li, Dan Tian, Jing Cen, Lian Duan, Weibo Xia   +4 more
openalex   +1 more source

Venous thromboembolism and severe hypernatremia in a patient with lithium-induced nephrogenic diabetes insipidus and acute kidney injury: a case report [PDF]

, 2021
Young Jin Goo, Su Hyun Song, Oh Il Kwon, Minah Kim, Sang Heon Suh, Tae Ryom Oh, Hong Sang Choi, Eun Hui Bae, Seong Kwon, Soo Wan Kim, Chang Seong Kim   +10 more
openalex   +1 more source

Current treatment of hereditary nephrogenic diabetes insipidus in children [PDF]

Childhood Kidney Diseases
Nephrogenic diabetes insipidus (NDI) is a rare disorder characterized by the inability of the kidneys to respond to arginine vasopressin, leading to polyuria, polydipsia, and chronic dehydration.
Jin-Soon Suh
doaj   +1 more source

Nephrogenic diabetes insipidus associated with a new mutation in the AVPR2 gene

Ожирение и метаболизм
Diabetes insipidus (DI) is an orphan disease clinically characterized by profound thirst and the excretion of large volumes of dilute urine. Nephrogenic diabetes insipidus (NDI) is characterized by resistance to the action of antidiuretic hormone (ADH ...
Y. A. Aleynikova, M. S. Berlovich, E. A. Pigarova, L. K. Dzeranova, M. S. Pankratova   +4 more
doaj   +1 more source

Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling [PDF]

, 2018
Yılmaz Kör, Minjing Zou, Roua A. Al‐Rijjal, Dorota Monies, Brian F. Meyer, Yufei Shi   +5 more
openalex   +1 more source

Effects of YM087 and VPA985 on the T237M mutant receptor functionality in nephrogenic diabetes insipidus

Türk Biyokimya Dergisi
Mutations detected in the AVPR2 gene (arginine vasopressin type 2 receptor) are known to cause nephrogenic diabetes insipidus (NDI). Several pharmacological chaperones (PCs) target misfolded AVPR2 proteins and rescue them from the quality control system ...
Avcu Elif Merve, Erdem Tuncdemir Beril, Saglar Ozer Emel   +2 more
doaj   +1 more source

Severe lithium-induced nephrogenic diabetes insipidus: The diuresis paradox

South African Medical Journal
We report a case of profound nephrogenic diabetes insipidus (NDI) in which renal resistance to antidiuretic hormone results in dilute polyuria despite normal circulating concentrations.
G S Tatz, Marc Blockman, J A Dave, I L Ross   +3 more
doaj   +1 more source

Dynamics and energetics of water transport through aquaporin mutants causing nephrogenic diabetes insipidus (NDI): A molecular dynamics study

, 2020
Hooman Hadidi, Reza Kamali, Alireza Binesh   +2 more
openalex   +2 more sources

Activation of AQP2 water channels without vasopressin: therapeutic strategies for congenital nephrogenic diabetes insipidus [PDF]

, 2018
Fumiaki Ando, Shinichi Uchida
openalex   +1 more source