Identification of a novel large deletion mutation in the <i>AVPR2</i> gene responsible for hereditary nephrogenic diabetes insipidus in an infant: a case report. [PDF]
Huang Y +5 more
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Novel AVPR2 mutations in congenital nephrogenic diabetes insipidus: clinical characteristics and genetic analysis. [PDF]
Xue K +5 more
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CKD in a Young Man with Nephrogenic Diabetes Insipidus. [PDF]
Teitelbaum I.
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Nephrogenic Diabetes Insipidus
Contains fulltext : mmubn000001_101473788.pdf (Publisher’s version ) (Open Access)
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NEPHROGENIC DIABETES INSIPIDUS: THE CRUCIAL ROLE OF AQUAPORINS
Nephrogenic diabetes insipidus (NDI) is a disorder marked by the kidney's inability to concentrate urine despite normal or elevated levels of vasopressin, often due to impairments in aquaporin-2 (AQP2) expression or function.
Hassan Yar Mahsood, Humayun Ali
doaj
Case Report of Nephrogenic Diabetes Insipidus with a Novel Mutation in the <i>AQP2</i> Gene. [PDF]
Padilla-Guzmán A +5 more
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A case of nephrogenic diabetes insipidus likely caused by anti-neutrophil cytoplastic antibody-associated vasculitis. [PDF]
Asakura K +5 more
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Nephrogenic Diabetes Insipidus Associated with Temozolomide Therapy in a Patient with Grade IV Astrocytoma. [PDF]
Fargouche Z +4 more
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Bendamustine-induced nephrogenic diabetes insipidus - A case report. [PDF]
Desjardins A +7 more
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