Results 71 to 80 of about 1,031,173 (193)

About Insipidus Syndrome in Pediatric Practice

open access: yesZdorovʹe Rebenka, 2013
В статье приведены данные об этиологии, патогенезе, клинике и дифференциальной диагностике инсипидарного синдрома, а также описан случай собственного клинического наблюдения нефрогенного несахарного диабета у мальчика 17 лет.
M.S. Ostropolets   +2 more
doaj   +1 more source

Primary Hyperparathyroidism in a Pregnant Immigrant Facing Healthcare Hurdles: A Case Report

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Introduction PHPT in pregnancy is a rare condition that may be difficult to recognize due to nonspecific symptoms and physiologic changes that can mask hypercalcemia. Delayed diagnosis is associated with significant maternal and fetal morbidity. Case Presentation A 36‐year‐old Spanish‐speaking gravida 5 para 3 woman at 30 weeks gestation presented with
Racquel McCrary   +5 more
wiley   +1 more source

Limits to the “Medical Clearance” of Patients Presenting With Psychiatric Changes: A Case Report and Review of the Literature

open access: yesCase Reports in Psychiatry, Volume 2026, Issue 1, 2026.
We discuss a case of a 54‐year‐old woman with a history of schizoaffective disorder and Parkinson’s disease who presented with altered mental status, including weakness, falls, medication refusal, and paranoia, heralding medical deterioration. The treating teams initially suspected that this presentation was medically driven, and she had multiple ...
Jordan Pelc   +3 more
wiley   +1 more source

Method of treatment of nephrogenic diabetes insipidus

open access: yes, 2010
Nephrogenic diabetes insipidus is treated with ...
PROCINO, Giuseppe   +3 more
core  

Vasopressin V2 receptor-related pathologies: congenital nephrogenic diabetes insipidus and nephrogenic syndrome of inappropiate antidiuresis

open access: yes, 2014
International audienceCongenital nephrogenic diabetes insipidus is a rare hereditary disease with mainly an X-linked inheritance (90% of the cases) but there are also autosomal recessive and dominant forms.
Morin, Denis
core   +1 more source

Prevalence and Characteristics of Deoxycholate and Liposomal Amphotericin B Adverse Reactions in a Third‐Level Care Hospital: A Retrospective Observational Study

open access: yesJournal of Clinical Pharmacy and Therapeutics, Volume 2026, Issue 1, 2026.
Background We aimed to establish the prevalence of adverse reactions associated with the use of deoxycholate and/or liposomal amphotericin B and to determine adherence to World Health Organization (WHO) recommendations to minimize the risk of toxicity. Methods Clinical data were collected from records of 143 patients over 18 years of age who were under
Thalia Berenice Jacobo Vargas   +7 more
wiley   +1 more source

Perioperative Management of Lithium Therapy: Considerations and Recommendations

open access: yes
Bipolar Disorders, Volume 28, Issue 1, February 2026.
L. S. Dominicus   +5 more
wiley   +1 more source

[Hereditary nephrogenetic diabetes insipidus--case report and discussion]

open access: yes, 2009
The history of a patient with hereditary nephrogenic diabetes insipidus is discussed.
Kruse, Anja, Solcà, Curzio
core  

Nephrogenic Diabetes Insipidus with Intracranial Calcifications in a Child with Thalassemia Minor [PDF]

open access: yes, 2013
Introduction: There are numerous causes for intracranial calcification in children. We describe an unusual cause of intracranial calcifications in a child, namely, nephrogenic diabetes insipidus (NDI).Case Report: A 12-year-old boy presented with ...
Alka, J, Dimple, J, Mona, G, Atul, D
core   +1 more source

Lithium intoxication and nephrogenic diabetes insipidus: a case report and review of literature

open access: yes, 2013
Abdulsamet Erden, Hatice Karagöz, Mustafa Başak, Samet Karahan, Ali Çetinkaya, Deniz Avci, Irfan Buğday Kayseri Training and Research Hospital, Internal Medicine Department, Kayseri, Turkey Abstract: Lithium is one of the drugs used widely in
Karahan S   +6 more
core  

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