Results 111 to 120 of about 35,448 (309)

Probable primary polydipsia in a domestic shorthair cat

Journal of Feline Medicine and Surgery Open Reports, 2015
Case summary A 10-month-old neutered male domestic shorthair cat presented with a 4 month history of polyuria and polydipsia. After a thorough diagnostic work-up the only abnormal findings were hyposthenuria and an elevated random plasma osmolality level.
Charles Tyler Long, Morika Williams, Mason Savage, Jonathan Fogle, Rick Meeker, Lola Hudson   +5 more
doaj   +1 more source

A Case of Psychogenic Polydipsia in an Elderly: An Overlooked Diagnosis [PDF]

Journal of Clinical and Diagnostic Research
Primary polydipsia, or psychogenic polydipsia, is characterised by excessive fluid intake without an underlying physiological cause. If left untreated, primary polydipsia may result in life-threatening hyponatremia and can lead to complications such as ...
Bhumika Vaishnav, Harshitha Ummaleti, Saish Mondkar, Bhavin Sanghani, Kshitij   +4 more
doaj   +1 more source

NPY Levels In Type 1 Diabetic Men of Different Duration. [PDF]

, 2011
Background: The aim of the present study was to evaluate whether the different duration of type 1 diabetes mellitus influences basal NPY secretion. Design: The NPY concentrations were measured in sixty-eight men with insulin-dependent diabetes mellitus ...
Anna Araldi, Claudio Giumelli, Lavinia Volpi, Luigi Capretti, Maria Grazia Magotti, Paolo Chiodera, Riccardo Volpi, Roberta Minelli, Simona Cataldo, Teore Ferri, Vittorio Coiro   +10 more
core   +1 more source

Schedule-Induced Polydipsia: Searching for the Endophenotype of Compulsive Behavior

, 2014
The development of excessive and persistent drinking under intermittent food-reinforcement schedules, known Schedule-induced polydipsia (SIP), has been proposed as a successful animal model to study compulsive behaviors.
P. Flores, Ana Sánchez-Kuhn, A. Merchán, Olga Vilches, Sergio García-Martín, M. Moreno   +5 more
semanticscholar   +1 more source

An Atypical Presentation of Bartter Syndrome Type 3 With Hypocalciuria and Opisthotonus Posture in a Preterm Infant

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT This case highlights an unusual presentation of Bartter Syndrome Type 3 marked by hypocalciuria and opisthotonus posture. Recognizing such atypical neuromuscular signs is essential for early diagnosis, genetic confirmation, and targeted management in pediatric patients with electrolyte imbalances.
Karim Hassan, Imad Afara, Ali Harajli, Jawad Allam, Kaity Saliba, Frederic Harb   +5 more
wiley   +1 more source

Pioglitazone Prevents Capillary Rarefaction in Streptozotocin-Diabetic Rats Independently of Glucose Control and Vascular Endothelial Growth Factor Expression [PDF]

, 2012
Background/Aims: Reduction of capillary network density occurs early in the development of metabolic syndrome and may be relevant for the precipitation of diabetes.
Andreas Dendorfer, Arany Z, Astrid Ashoff, Baraka A, Battegay EJ, Billiet L, Biscetti F, Blasi ER, Chintalgattu V, Cipolla MJ, Dendorfer A, Duan SZ, Emanueli C, Emoto M, Fatimunnisa Qadri, Frisbee JC, Frisbee JC, Frisbee JC, Gealekman O, Geraldes P, Goodwill AG, Han B, Heidbreder M, Kobayashi N, Levy BI, Lillioja S, Lindenmeyer MT, Nishikawa T, Noon JP, Ohga S, Olaf Jöhren, Polikandriotis JA, Prewitt RL, Redondo S, Reinhard Eggers, Romeo G, Son NH, Thangarajah H, Vogt CJ, Walter Raasch, Weidner N, Yue Tl TL, Zolk O   +42 more
core   +1 more source

Prognosis and Phenotypes of Advanced Head and Neck Carcinoma Associated With Hypercalcemia

Head &Neck, Volume 47, Issue 8, Page 2174-2182, August 2025.
ABSTRACT Purpose Hypercalcemia is the most common metabolic disorder in cancer, affecting 10%–20% of patients with advanced malignancies, including squamous cell carcinoma of the head and neck (HNSCC), though its prognostic significance remains poorly studied.
Elodie Mamou, Paul Gougis, Baptiste Abbar, Jean‐philippe Spano, Laetitia Morardet, Aurore Vozy   +5 more
wiley   +1 more source

A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East. [PDF]

, 2019
Background: Nephropathic Cystinosis, the most common cause of renal Fanconi syndrome, is a lysosomal transport disorder with an autosomal recessive inheritance pattern. A large number of mutations in CTNS have been identified as causative to date.
Aldahmesh, Anikster, Bastug, Bertholet-Thomas, Cherqui, Chkioua, Cogan, Doneray, Elmonem, Emma, Forestier, Gahl, Gahl, Ghazi, Goldman, Higashi, Jaradat, Kalatzis, Kleta, Levy, McDowell, Sadeghipour, Servais, Shahkarami, Soliman, Thoene, Topaloglu, Topaloglu, Wamelink, Wilmer, Yang, Yeetong, Önenli-Mungan   +32 more
core   +3 more sources

Copeptin in the differential diagnosis of the polydipsia-polyuria syndrome--revisiting the direct and indirect water deprivation tests.

Journal of Clinical Endocrinology and Metabolism, 2011
BACKGROUND The water deprivation test (WDT) with direct or indirect measurement of plasma arginine vasopressin (AVP) is the method of choice for the differential diagnosis of the polydipsia-polyuria syndrome.
W. Fenske, M. Quinkler, D. Lorenz, K. Zopf, U. Haagen, J. Papassotiriou, A. Pfeiffer, M. Fassnacht, S. Störk, B. Allolio   +9 more
semanticscholar   +1 more source

Juvenile nephropathy resembling human nephronophthisis–medullary cystic kidney disease in a 9‐month‐old domestic shorthaired cat

Journal of Small Animal Practice, EarlyView.
N. Goody, J. Poldy, A. Malbon, T. Morrison, I. Montanes‐Sancho, S. Dancer, D. Gunn Moore   +6 more
wiley   +1 more source