Results 1 to 10 of about 6,338,781 (311)

Growth and Overall Health of Patients with SLC13A5 Citrate Transporter Disorder

open access: yesMetabolites, 2021
We were interested in elucidating the non-neurologic health of patients with autosomal recessive SLC13A5 Citrate Transporter (NaCT) Disorder. Multiple variants have been reported that cause a loss of transporter activity, resulting in significant ...
Tanya L. Brown   +2 more
doaj   +1 more source

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

open access: yesFrontiers 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   +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

open access: yesFrontiers 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   +12 more
doaj   +1 more source

Journal Staff [PDF]

open access: yes, 2012
There are fewer longitudinal studies from China on symptoms as described for the sick building syndrome (SBS). Here, we performed a two-year prospective study and investigated associations between environmental parameters such as room temperature ...
Li, Fan   +4 more
core   +10 more sources

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

open access: yesIranian 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   +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

open access: yesFrontiers 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   +6 more
doaj   +1 more source

The role of posttraumatic stress and depression symptoms in mother-infant bonding [PDF]

open access: yes, 2020
Background: There is some evidence posttraumatic stress disorder (PTSD) following childbirth may impact on the mother-infant bond. However, the evidence is inconsistent over whether PTSD or co-morbid depressive symptoms are primarily related to impaired ...
Anđelinović, M.   +4 more
core   +1 more source

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

open access: yesFrontiers 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   +3 more
doaj   +1 more source

Depressive symptoms in cancer patients compared with people from the general population: the role of sociodemographic and medical factors [PDF]

open access: yes, 2003
This study examined depressive symptoms in 475 patients with cancer and in a reference group of 255 individuals without cancer from the general population and the associations of those symptoms with sociodemographic and medical factors.
Ranchor, A.V.   +2 more
core   +6 more sources

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

open access: yesFrontiers 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   +16 more
doaj   +1 more source

Home - About - Disclaimer - Privacy