Results 11 to 20 of about 4,332,955 (318)

Development and User Experiences of a Biopsychosocial Interprofessional Online Course on Persistent Somatic Symptoms

Frontiers in Psychiatry, 2021
Background: Communication between healthcare providers and patients with persistent somatic symptoms (PSS) is frequently hampered by mutual misunderstanding and dissatisfaction.Methods: We developed an online, interprofessional course to teach healthcare
A. van Gils, L. M. Tak, H. Sattel, J. G. M. Rosmalen, J. G. M. Rosmalen   +4 more
doaj   +1 more source

Observational case-control study of small-fiber neuropathies, with regards on smoking and vitamin D deficiency and other possible causes

Frontiers in Medicine, 2023
IntroductionSmall fiber neuropathies (SFNs) are disorders of skin nerve endings inducing pruritus, burning pain, numbness, and paresthesia. The aims of this study were to search for putative etiologies of SFN and their occurrence in a cohort of patients ...
Maxime Fouchard, Maxime Fouchard, Emilie Brenaut, Emilie Brenaut, Steeve Genestet, Steeve Genestet, Anne-Sophie Ficheux, Pascale Marcorelles, Pascale Marcorelles, Pascale Marcorelles, Laurent Misery, Laurent Misery, Laurent Misery   +12 more
doaj   +1 more source

Rigid Bronchoscopy in Foreign Bodies Aspiration: Value of the Clinical and Radiological Findings [PDF]

Iranian Journal of Neonatology, 2023
Background: Foreign body aspiration (FBA) is an emergency condition in children, potentially leading to  life-threatening events. The gold standard for FBA management typically involves rigid bronchoscopy (RB).
Arash Azadmehr, Behnamreza Makhsosi, Soleyman Mohammadi, Mehrasa Yousefi, Sara Darvishi-Shani   +4 more
doaj   +1 more source

Characterizing a rare neurogenetic disease, SLC13A5 citrate transporter disorder, utilizing clinical data in a cloud-based medical record collection system

Frontiers in Genetics, 2023
Introduction: SLC13A5 citrate transporter disorder is a rare autosomal recessive genetic disease that has a constellation of neurologic symptoms. To better characterize the neurologic and clinical laboratory phenotype, we utilized patient medical records
Emily M. Spelbrink, Tanya L. Brown, Elise Brimble, Kirsten A. Blanco, Kirsten A. Blanco, Kimberly L. Nye, Brenda E. Porter   +6 more
doaj   +1 more source

Steps Towards Developing Effective Treatments for Neuropsychiatric Disturbances in Alzheimer’s Disease: Insights From Preclinical Models, Clinical Data, and Future Directions

Frontiers in Aging Neuroscience, 2020
Alzheimer’s disease (AD) is the most common form of dementia worldwide. It is mostly known for its devastating effect on memory and learning but behavioral alterations commonly known as neuropsychiatric disturbances (NPDs) are also characteristics of the
Amalie Clement, Amalie Clement, Ove Wiborg, Ayodeji A. Asuni   +3 more
doaj   +1 more source

Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial

BMC Psychiatry, 2018
Background Comorbid psychiatric disorders are frequent in children with intellectual disability (ID). Given the limitations of drugs treatments, cognitive remediation could be a promising tool to reduce these challenging behaviors but evidence is still ...
Emilie Favre, Elodie Peyroux, Marie-Noelle Babinet, Alice Poisson, Caroline Demily   +4 more
doaj   +1 more source

The Relationship Between Childhood Trauma and the Response to Group Cognitive-Behavioural Therapy for Chronic Fatigue Syndrome

Frontiers in Psychiatry, 2020
ObjectiveTo examine the relationship between childhood trauma and the response to group cognitive-behavioural therapy (GCBT) for chronic fatigue syndrome (CFS).MethodsA single cohort study conducted in an outpatient university referral center for CFS ...
Maud De Venter, Maud De Venter, Jela Illegems, Jela Illegems, Rita Van Royen, Rita Van Royen, Bernard G. C. Sabbe, Greta Moorkens, Greta Moorkens, Filip Van Den Eede, Filip Van Den Eede, Filip Van Den Eede   +11 more
doaj   +1 more source

COVID-19 encephalopathy with severe neurological symptoms: a clinical case presentation with literature review

Neurologijos seminarai, 2023
COVID-19 infection is affecting more and more people around the world, and as the number of recovered patients increases, so does the knowledge on the potential clinical signs of the disease.
G. Baranauskienė, N. Tutlienė, G. Kaubrys   +2 more
doaj   +1 more source

Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings

Frontiers in Neurology, 2018
The ryanodine receptor 1-related congenital myopathies (RYR1-RM) comprise a spectrum of slow, rare neuromuscular diseases. Affected individuals present with a mild-to-severe symptomatology ranging from proximal muscle weakness, hypotonia and joint ...
Joshua J. Todd, Muslima S. Razaqyar, Jessica W. Witherspoon, Tokunbor A. Lawal, Ami Mankodi, Irene C. Chrismer, Carolyn Allen, Mary D. Meyer, Anna Kuo, Monique S. Shelton, Kim Amburgey, Dmitriy Niyazov, Pierre Fequiere, Carsten G. Bönnemann, James J. Dowling, James J. Dowling, Katherine G. Meilleur   +16 more
doaj   +1 more source

COVID-19 and recurrent respiratory infections in children of Kazakhstan

Russian Open Medical Journal, 2021
The study goal was to investigate the COVID-19 clinical course in children with recurrent respiratory infections (RRI) in Nur-Sultan, Kazakhstan. Material and Methods — we conducted the retrospective analysis of 94 children with RRI, diagnosed with ...
Adil Zhamankulov, Rafail Rozenson, Marina Morenko, Kseniya Shnayder, Ulzhan Akhmetova, Alina Tyo   +5 more
doaj   +1 more source