Results 21 to 30 of about 1,257 (102)

Two Cases of Diabetes Insipidus in Lactating Parents With Low Milk Supply Whose Infants Showed Growth‐Faltering: Was Diabetes Insipidus a Possible Cause?

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, McKenzie Yuhyun Yun, Bridget Young, Casey Rosen-Carole, Seung-Yup Ku   +4 more
wiley   +1 more source

Polymicrobial Osteomyelitis in a Patient With Isolation of Trueperella bernardiae: A Case Report and Literature Review

Case Reports in Infectious Diseases, Volume 2025, Issue 1, 2025.
Background: Trueperella bernardiae is a Gram‐positive rod that has been described as an opportunistic pathogen in immunocompromised patients. In a significant number of documented cases, infections with Trueperella bernardiae have been associated with polymicrobial infections, which highlight the fact that important bacteria–bacteria relations might be
Marco Antonio Delaye-Martínez, Edgar Samuel Vanegas-Rodríguez, Braulio Mendez-Sotelo, María de Lourdes García-Hernández, Claudia Adriana Colín-Castro, Rafael Franco-Cendejas, Luis Esaú López-Jácome, Piyush Baindara   +7 more
wiley   +1 more source

A Rare Case of Central Diabetes Insipidus in a Pediatric Patient

Acta Médica Portuguesa
N/a.
Ana Raquel Henriques, Miguel M. Lopes, Brígida Robalo, Carla Pereira, Maria de Lurdes Sampaio   +4 more
doaj   +1 more source

Topology of WFS1 Variants Linked With Islet Function and Higher Risk of Urological Symptoms in WFS1‐Associated Disease

Pediatric Diabetes, Volume 2025, Issue 1, 2025.
Wolfram syndrome type 1 gene (WFS1), which encodes a transmembrane (TM) structural protein (wolframin), is essential for several biological processes. Mutations of WFS1, autosomal dominant or recessive inherited, are related to a broad clinical spectrum. Molecular genetic tests were performed, and clinical phenotypes of three WFS1‐associated cases were
Juan-juan Zhang, Tong-tong Dai, Jun-qi Wang, Ming-yue Yin, Yuan-yan Yang, Li Jiang, Bei-jun Xia, Zhuo-zhou Cui, Wen-li Lu, Rong-gui Hu, Chuan-yin Li, Zhi-ya Dong, Yuan Xiao, Rasha Hamza   +13 more
wiley   +1 more source

Preterm birth and risk of hospitalisation for complex chronic conditions during childhood and adolescence

Acta Paediatrica, Volume 113, Issue 12, Page 2610-2618, December 2024.
Abstract Aim To examine the relationship between preterm birth and hospitalisation for paediatric complex chronic conditions. Methods We conducted a cohort study of 1 269 745 children born between 2006 and 2022 in Quebec, Canada. We classified preterm birth as extreme (<28 weeks), very (28–31 weeks), and moderate (32–36 weeks).
Gabriel Côté‐Corriveau, Juliette St‐Georges, Thuy Mai Luu, Aimina Ayoub, Nathalie Auger   +4 more
wiley   +1 more source

A Case report of Wolfram Syndrome

مجله دانشگاه علوم پزشکی بیرجند, 2013
Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease should be suspected if non-autoimmune insulin-dependent diabetes occurs in an under-sixteen year old person having bilateral optic nerve atrophy. Diabetes
Samaneh Norooziasl, Seyed Alireza Javadinia   +1 more
doaj  

A better understanding of basic science may help our management of LUTS/LUTD in older persons with nocturnal polyuria and nocturia: ICI‐RS 2024

Neurourology and Urodynamics, Volume 43, Issue 8, Page 2300-2307, November 2024.
Abstract Aims To discuss the role of autocrine/paracrine signaling of urothelial arginine vasopressin (AVP) on mammalian bladder capacities and micturition thresholds, impact of distension on water/urea reabsorption from the bladder, review of the literature to better characterize the central/peripheral effects of AVP, desmopressin (dAVP) toxicity, and
Anthony Kanai, Karel Everaert, Apostolos Apostolidis, Christopher Fry, Pradeep Tyagi, Andries Van Huele, Bahareh Vahabi, Wendy Bower, Alan Wein, Paul Abrams   +9 more
wiley   +1 more source

Central diabetes insipidus: alert for dehydration in very low birth weight infants during the neonatal period. A case report

São Paulo Medical Journal
CONTEXT: Central diabetes insipidus (CDI) is a rare cause of hypernatremia during the neonatal period. The diagnosis is particularly difficult in very low birth weight (VLBW) newborns.
Maria Lúcia Silveira Ferlin, Débora Simone Sales, Fábia Pereira Martins Celini, Carlos Eduardo Martinelli Junior   +3 more
doaj   +1 more source

Arginine vasopressin in mood disorders: A potential biomarker of disease pathology and a target for pharmacologic intervention

Psychiatry and Clinical Neurosciences, Volume 78, Issue 9, Page 495-506, September 2024.
Vasopressin or arginine‐vasopressin (AVP) is a neuropeptide molecule known for its antidiuretic effects and serves to regulate plasma osmolality and blood pressure. The existing literature suggests that AVP plays a multifaceted—though less well‐known—role in the central nervous system (CNS), particularly in relation to the pathophysiology and treatment
Hiroe Hu, Carlos A. Zarate Jr, Joseph Verbalis   +2 more
wiley   +1 more source

ECEIM consensus statement on equine kidney disease

Journal of Veterinary Internal Medicine, Volume 38, Issue 4, Page 2008-2025, July/August 2024.
Abstract The aim of this consensus statement is to summarize and appraise scientific evidence and combine this with the clinical experience of a panel of experts to optimize recommendations on how to recognize and manage kidney disease in horses.
Gaby van Galen, Thomas J. Divers, Victoria Savage, Harold C. Schott II, Natalia Siwinska   +4 more
wiley   +1 more source