Results 21 to 30 of about 2,892 (190)
Central Diabetes Insipidus in an Extremely-Low-Birth-Weight Preterm Infant with Suspected Ectopic Posterior Lobe of the Pituitary Gland [PDF]
Neonatal Medicine, 2020 Central diabetes insipidus (CDI) is extremely rare in neonates, especially in extremely-low-birth-weight infants, and most cases are secondary to conditions, such as ischemic or hemorrhagic brain damage.
Yung Zu Park +5 more
doaj +1 more source
International Journal of Paediatric Dentistry, Volume 33, Issue 6, Page 543-552, November 2023., 2023 Abstract Background Molar‐root incisor malformation (MRIM) is a rare dental anomaly featuring constricted cervical margins and tapered, narrow root and pulp morphology, often associated with severe toothache and infection. Aim The aim of this study was to determine the prevalence of MRIM in children seen in a specialist paediatric dental unit of a ...
Emilija D. Jensen +6 more
wiley +1 more source
Advanced Sensoring Technologies for Evaluation and Management of Lower Urinary Tract Symptoms
Advanced Sensor Research, Volume 2, Issue 9, September, 2023., 2023 Sensors have become important tools for dealing with various diseases. This review summarizes the sorts of sensors that can be used in the diagnosis and treatment of lower urinary tract symptoms (LUTS). Meanwhile, combined with various etiologies of LUTS, the working principle and significance of the sensors are introduced.
Haitao Gong +4 more
wiley +1 more source
Updated consensus guidelines on the management of Phelan–McDermid syndrome
American Journal of Medical Genetics Part A, Volume 191, Issue 8, Page 2015-2044, August 2023., 2023 Abstract Phelan–McDermid syndrome (PMS) is a genetic condition caused by SHANK3 haploinsufficiency and characterized by a wide range of neurodevelopmental and systemic manifestations. The first practice parameters for assessment and monitoring in individuals with PMS were published in 2014; recently, knowledge about PMS has grown significantly based on
Siddharth Srivastava +44 more
wiley +1 more source
Presumed pituitary apoplexy in 26 dogs: Clinical findings, treatments, and outcomes
Journal of Veterinary Internal Medicine, Volume 37, Issue 3, Page 1119-1128, May/June 2023., 2023 Abstract Background Pituitary apoplexy refers to hemorrhage or infarction within the pituitary gland resulting in acute neurological abnormalities. This condition is poorly described in dogs. Objectives To document presenting complaints, examination findings, endocrinopathies, magnetic resonance imaging (MRI), treatments, and outcomes of dogs with ...
Christian W. Woelfel +8 more
wiley +1 more source
A Case of Lithium Encephalopathy with Therapeutic Lithium Levels: The Diagnostic Role of EEG
Case Reports in Psychiatry, Volume 2022, Issue 1, 2022., 2022 Introduction. Lithium is considered a first‐line therapy for both the acute phase and the maintenance of bipolar disorder. Many studies highlighted its neuroprotective and neuroplastic capacity suggesting a potential usefulness in the treatment of neurodegenerative diseases.
Claudia Carmassi +7 more
wiley +1 more source
Variable Expressivity of Wolfram Syndrome in a Family with Multiple Affected Subjects [PDF]
, 2021 Purpose: To study the genetic basis and clinical manifestations of Wolfram syndrome in a multi-affected family. Methods: Complete clinical examinations including urological, ophthalmic, neurological, and endocrinologic assessment were performed for three
Doozandeh, Azadeh +4 more
core +2 more sources
Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2. [PDF]
, 2016 CONTEXT: Nephrogenic syndrome of inappropriate antidiuresis (NSIAD), resulting from activating mutations in the arginine vasopressin receptor type 2 (AVPR2), is a rare cause of hyponatraemia.
Adrogué +35 more
core +2 more sources
Genetic forms of neurohypophyseal diabetes insipidus [PDF]
, 2020 In the majority of cases, hereditary neurohypophyseal diabetes insipidus (DI) is a monogenic disorder caused by mutations in the AVP gene. Dominant transmission is by far the most common form. In these patients, symptoms develop gradually at various ages
Beuret, Nicole +2 more
core +1 more source
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