Results 21 to 30 of about 1,226 (139)
Translational Research for Pediatric Lower Urinary Tract Dysfunction [PDF]
International Neurourology Journal, 2016 This review provides a comprehensive view of translational research aimed at elucidating the pathophysiology of pediatric lower urinary tract dysfunction (LUTD).
Akihiro Kanematsu
doaj +1 more source
Saudi Journal of Kidney Diseases and Transplantation, 2018 Systemic lupus erythematosus (SLE) presenting as diabetes insipidus (DI) is a rare association; there is a case report of neurogenic DI in patients of SLE; however, SLE and nephrogenic DI has not been reported in literature.
Ashaq Hussain Parrey +3 more
doaj +1 more source
Transient Diabetes Insipidus Following Thermal Burn; A Case Report and Literature Review [PDF]
Bulletin of Emergency and Trauma, 2017 Diabetes insipidus is a disease charaterised by increased urine production and thrist. Neurogenic diabetes insipidus following head trauma,autoimmune disease and infection is quite common but diabetes insipidus following thermal burn injury is a rare ...
Suvashis Dash, Shibajyoti Ghosh
doaj
The 2023 World Small Animal Veterinary Association (WSAVA)
, 2023 Journal of Small Animal Practice, Volume 64, Issue 12, Page 731-748, December 2023.
P. V. Steagall +9 more
wiley +1 more source
Kidney International, 1979 A 15-year-o1d girl was admitted to the New England Medical Center Hospital (NEMCH) for investigation of the hypothalamic-pituitary axis. Four years earlier, an eosinophilic granuloma was discovered in the left mandible and was treated with excision and irradiation (1000 rads).
openaire +1 more source
282 NEUROGENIC DIABETES INSIPIDUS IN NEWBORN INFANTS ASSOCIATED WITH CNS ABNORMALITIES [PDF]
Pediatric Research, 1978 The clinical syndrome of neurogenic diabetes insipidus (DI) has recently been observed in three neonates. All cases were the products of complicated labors and deliveries and manifested symptoms of DI in the first 72 hours of life. Associated CNS abnormalities included metabolic encephalopathy, hemorrhage and cerebral hypoxia.
David R Brown +2 more
openaire +1 more source
Late onset of familial neurogenic diabetes insipidus in monozygotic twins
Endocrine Regulations, 2013 Autosomal dominant familial diabetes insipidus (FNDI) is a rare disease characterized by polydipsia and polyuria due to deficiency of the antidiuretic hormone, arginine vasopressin (AVP). We report the first Slovak family with the disease. Noteworthy is the concordantly belated debut of the disease symptoms in two monozygotic twin proband girls in the ...
M, Cizmarova +6 more
openaire +2 more sources
Neurogenic diabetes insipidus in patients with systemic lupus erythematosus
Annals of the Rheumatic Diseases, 1998 Neurogenic diabetes insipidus (NDI) approximately affects one of 25 000 people. The idiopathic type represents about 30% of all NDI cases (one of 75 000).1 The coexistence of primary NDI and systemic lupus erythematosus (SLE) is an exceptional fact that has not been previously described.
JULIO SÁNCHEZ-ROMÁN +4 more
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Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.Diabetes insipidus (DI) is a disorder of the hypothalamic‐pituitary axis resulting in abnormal sodium (Na) balance, dilute urine, and hypertonic dehydration. DI may impact lactation by impacting hormones necessary for lactation maintenance or through DI‐related alterations in pituitary function and Na metabolism. Two lactating mothers with DI presented
Erica Nicasio +4 more
wiley +1 more source
Advances in Research, 2023 To report and review a case of prolactin-producing pituitary tumor presenting with mass effects, hormonal deficiency, and neurogenic diabetes insipidus in a nulliparous woman of Afro-Caribbean descent. The patient presented with dull-aching headaches associated with worsening vision, nausea, and vomiting.
Adedeji Okikiade +5 more
openaire +1 more source