Results 101 to 110 of about 8,417 (217)

Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: Additional findings or a new syndrome (ARCC-NDI)? [PDF]

, 1997
Rosalind Coleman, Johan L.K. Van Hove, C. Richard Morris, J. Marc Rhoads, Marshall Summar   +4 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

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

Nephrogenic Diabetes Insipidus following an Off-Label Administration of Sevoflurane for Prolonged Sedation in a COVID-19 Patient and Possible Influence on Aquaporin-2 Renal Expression [PDF]

, 2022
Camie Dupuis, Arnaud Robert, Ludovic Gérard, Johann Morelle, Pierre‐François Laterre, Philippe Hantson   +5 more
openalex   +1 more source

Síndrome poliuria-polidipsia : ¿Como abordaría el diagnóstico? [PDF]

, 1989
El síndrome poliuria-polidipsia (PU/PD) es una entidad clínica que se presenta como signo predominante de numerosos procesos del perro y del gato. Tras un recuerdo fisiológico de los factores reguladores de la homeostasis del agua, presentamos las ...
Aceña Fabián, M. Carmen, Aznar Chicote, J., Díez González, R., García-Belenguer, Sylvia, Marca Andrés, Mª C., Verde Arribas, Mª T.   +5 more
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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

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

Congenital nephrogenic diabetes insipidus (NDI; also known as arginine vasopressin resistance) is a rare inherited disorder of water homeostasis, caused by insensitivity of the distal nephron to arginine vasopressin.
Arguedas Flores, Olga, Ariceta, Gema, Bichet, Daniel G., Bockenhauer, Detlef, Emma, Francesco, Hoorn, Ewout J., Knoers, Nine V.A.M., Koster-Kamphuis, Linda, Levtchenko, Elena, Nijenhuis, Tom, Trepiccione, Francesco, Vargas-Poussou, Rosa, Walsh, Stephen B.   +12 more
core   +3 more sources

Tubulointerstitial nephritis in primary Sjögren syndrome: clinical manifestations and response to treatment [PDF]

, 2016
BACKGROUND: Primary Sjögren syndrome (pSS) is a common autoimmune condition which primarily affects epithelial tissue, often including the kidney causing either tubulointerstitial nephritis (TIN) or more rarely, an immune complex related ...
Ciurtin, C, Evans, RD, Laing, CM, Walsh, SB   +3 more
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