Results 131 to 140 of about 23,590 (248)

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

open access: yesTürk 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   +2 more
doaj   +1 more source

Severe lithium-induced nephrogenic diabetes insipidus: The diuresis paradox

open access: yesSouth 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   +3 more
doaj   +1 more source

Using lithium [PDF]

open access: yes, 2006
Editorial; Comment in Hong Kong Medical Journal, 2006, v. 12 n. 4, p.
Tang, SW
core  

Differential diagnosis of diabetes insipidus syndrome on the example of clinical cases

open access: yesЛечащий Врач
Background. DDiagnosis of various forms of diabetes insipidus in childhood causes significant difficulties, as it is a complex multi-part process. The young age of patients often does not allow for a number of diagnostic tests, which makes it difficult ...
O. I. Krasnoperova   +2 more
doaj   +1 more source

Cancer and the Kidney [PDF]

open access: yes, 1978
Cancer of the kidney is associated with a bewildering array of extrarenal symptoms, and conversely, tumors far removed from the kidney produce intriguing renal functional abnormalities.
Oken, Donald E.
core   +1 more source

Is there a gender difference in antidiuretic response to desmopressin in children? [PDF]

open access: yes, 2013
De Bruyne, Pauline   +4 more
core   +1 more source

MODERN METHODS OF TREATMENT OF THE NEPHROGENIC FORM OF DIABETES INSIPUSIDUS IN CHILDREN [PDF]

open access: yes
Congenital nephrogenic diabetes insipidus (CNDI) is a hereditary tubulopathy, the leading symptoms of which are polyuria, polydipsia, and hyposternuria.
Charos, Xusanova   +4 more
core   +1 more source

International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)

open access: yesNature Reviews Nephrology
E. Levtchenko   +12 more
semanticscholar   +1 more source

A Pedigree Study of Hereditary Diabetes Insipidus Caused by X Chromosome AVPR2 Gene Mutation

open access: yesInternational Medical Case Reports Journal
Lei Li,* Yong Fan,* Guoli Du, Jing Xu, Sheng Jiang State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia; Department of Endocrinology, The First Affiliated Hospital of Xinjiang Medical ...
Li L, Fan Y, Du G, Xu J, Jiang S
doaj  

Structural and functional analysis of aquaporin-2 mutants involved in nephrogenic diabetes insipidus. [PDF]

open access: yesSci Rep, 2023
Hagströmer CJ   +6 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy