Results 271 to 280 of about 8,081,518 (357)
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron +5 more
wiley +1 more source
A systematic review of international performance indicators and metrics relevant to UK general practice. [PDF]
Chambers D +4 more
europepmc +1 more source
An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco +7 more
wiley +1 more source
Digital Information Sharing Before Consultations in General Practice: Protocol for a Scoping Review.
Razai MS +6 more
europepmc +1 more source
Evaluation of the Personality Disorder Positive Outcomes Programme (PDPOP) in general practice: an evaluation. [PDF]
Trueman H +3 more
europepmc +1 more source
Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein +13 more
wiley +1 more source
Exploring patient experiences with a mindfulness course in a general practice setting: a qualitative study. [PDF]
Dupont JK, Waldorff FB, Graungaard AH.
europepmc +1 more source

