Results 21 to 30 of about 2,210 (186)

Upper urinary dilatation and treatment of 26 patients with diabetes insipidus: A single-center retrospective study

Frontiers in Endocrinology, 2022
ObjectiveTo describe the urinary tract characteristics of diabetes insipidus (DI) patients with upper urinary tract dilatation (UUTD) using the video-urodynamic recordings (VUDS), UUTD and all urinary tract dysfunction (AUTD) systems, and to summarize ...
Xuesheng Wang, Xuesheng Wang, Xiaoqian Ying, Fan Zhang, Xing Li, Guoqing Chen, Zhonghan Zhou, Zhonghan Zhou, Limin Liao, Limin Liao, Limin Liao   +10 more
doaj   +1 more source

Prevalence and morphological features of molar‐root incisor malformation in children attending a specialist paediatric dental unit

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, Gabrielle Smart, Nara Lee, Jenny Tan, Kelly Oliver, William N. Ha, Sarbin Ranjitkar   +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, Zhenshan Ding, Binbin Jiao, Jian Ren, Qingsong Yu   +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, Mustafa Sahin, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Latha Valluripalli Soorya, Audrey Thurm, Jonathan A. Bernstein, Afua Asante‐Otoo, William E. Bennett Jr, Catalina Betancur, Tegwyn H. Brickhouse, Maria Rita Passos Bueno, Maya Chopra, Celanie K. Christensen, Jennifer L. Cully, Kira Dies, Kate Friedman, Brittany Gummere, J. Lloyd Holder Jr, Andres Jimenez‐Gomez, Carolyn A. Kerins, Omar Khan, Teresa Kohlenberg, Ronald V. Lacro, Lori A. Levi, Tess Levy, Diane Linnehan, Loth Eva, Baharak Moshiree, Ann Neumeyer, Scott M. Paul, Katy Phelan, Antonio Persico, Robert Rapaport, Curtis Rogers, Jeffrey Saland, Swathi Sethuram, Janine Shapiro, Phillip I. Tarr, Kerry M. White, Jordan Wickstrom, Kent M. Williams, Dana Winrow, Brian Wishart, Alexander Kolevzon   +44 more
wiley   +1 more source

Diabetes Insipidus with Hypoxic Encephalopathy

Pediatric Neurology Briefs, 1996
Neurogenic diabetes insipidus (DI) due to hypoxic encephalopathy is reported in 6 cases and 28 pediatric cases in the literature are reviewed from the Mackay Memorial Hospital, Taipei, Taiwan, ROC.
J Gordon Millichap
doaj   +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, Christopher L. Mariani, Michael W. Nolan, Erin K. Keenihan, Sophia P. Topulos, Peter J. Early, Karen R. Muñana, Sarah E. Musulin, Natasha J. Olby   +8 more
wiley   +1 more source

Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome

Journal of Current Ophthalmology, 2015
Purpose: To report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabetes insipidus, progressive optic atrophy, and deafness. Case report: A 19-year-old female patient, a known case of diabetes mellitus type I from six years before,
Nasrollah Maleki, Bahman Bashardoust, Anahita Zakeri, Azita Salehifar, Zahra Tavosi   +4 more
doaj   +1 more source

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

Systemic lupus erythematosus with Sjögren's syndrome and renal tubular acidosis presenting as nephrogenic diabetes insipidus

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, Fayaz Ahmad, Mushtaq Ahmad, Adil Basher   +3 more
doaj   +1 more source

Case Report: When an unknown fever unmasks Erdheim-Chester disease: a case showing the use of multimodality imaging and the successful interferon alpha therapy. [PDF]

F1000Res
Background Erdheim-Chester disease (ECD) is an extremely rare histiocytic neoplasm with a highly variable and often unpredictable clinical course and prognosis.
Boudriga H, Ben Hassine I, Ben Elkilani O, Sfar R, Ezzine A, Anoun J, Mzabi A, Ben Fredj F, Chatti K.   +8 more
europepmc   +2 more sources