Results 41 to 50 of about 88,226 (249)

A global multilingual cocreation of aphasia priority topics through patient and public involvement

open access: yesResearch Involvement and Engagement
Background People living with chronic aphasia (PWA) face long-term challenges that go well beyond communication difficulties, including emotional, social, and societal barriers.
Jean Marie Annoni   +12 more
doaj   +1 more source

Stroke‐Heart Syndrome: Mechanisms, Temporal Phenotypes, and Diagnostic Reasoning

open access: yesAdvanced Science, EarlyView.
Stroke‐heart syndrome describes new or worsened cardiac abnormalities after acute stroke. This Review defines its clinical boundaries, traces autonomic, inflammatory, endothelial, and supply‐demand mechanisms across time, and proposes provisional phenotypes that integrate lesion location, premorbid cardiac substrate, serial biomarkers ...
Fa Lin   +13 more
wiley   +1 more source

Establishing Quality Indicators and Implementation Priorities for Post‐Stroke Aphasia Services Through End‐User Involvement

open access: yesHealth Expectations
Background Currently, there are no agreed quality standards for post‐stroke aphasia services. Therefore, it is unknown if care reflects best practices or meets the expectations of people living with aphasia.
Kirstine Shrubsole   +11 more
doaj   +1 more source

Cerebral Small Vessel Disease in Immune‐Mediated Thrombotic Thrombocytopenic Purpura Patients During the Acute Phase and Disease Remission

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Immune‐mediated thrombotic thrombocytopenic purpura (iTTP) is a life‐threatening thrombotic microangiopathy characterized by acute neurological manifestations and long‐term sequelae related to microvascular brain injury. Cerebral small vessel disease (cSVD), detectable on MRI through lacunes, microbleeds, white matter hyperintensities, and ...
Addolorata Truma   +13 more
wiley   +1 more source

The association between cognitive and language skills in Catalan aphasia [PDF]

open access: yes, 2022
People with aphasia (PWA) often present other cognitive deficits (Caplan et al., 2013; Wall et al., 2017) argued to contribute to their linguistic impairment (Christensen et al., 2018; Choinski et al., 2020).
Muntané Sánchez, Helena   +2 more
core   +1 more source

Overcoming barriers and embedding processes to sustainably deliver high-dose post-stroke aphasia rehabilitation: a mixed methods longitudinal process evaluation

open access: yesBMC Health Services Research
Background Delivering evidence-based stroke rehabilitation in clinical practice is challenging due to intervention complexity and healthcare system factors.
Kirstine Shrubsole   +7 more
doaj   +1 more source

Bridging the digital divide for people with aphasia: a study protocol for codesigning web accessibility tools and guidelines

open access: yesBMJ Open
Introduction Aphasia is a language impairment that affects one-third of people who experience a stroke. Aphasia can impact all facets of language: speaking, understanding, reading and writing.
Leanne Togher   +14 more
doaj   +1 more source

Noun and verb processing in aphasia: Behavioural profiles and neural correlates

open access: yesNeuroImage: Clinical, 2018
The behavioural and neural processes underpinning different word classes, particularly nouns and verbs, have been a long-standing area of interest in psycholinguistic, neuropsychology and aphasiology research.
Reem S.W. Alyahya   +3 more
doaj   +1 more source

Treatment fidelity monitoring, reporting and findings in a complex aphasia intervention trial: a substudy of the Very Early Rehabilitation in SpEech (VERSE) trial

open access: yesTrials, 2022
Background Treatment fidelity is inconsistently reported in aphasia research, contributing to uncertainty about the effectiveness of types of aphasia therapy following stroke.
Erin Godecke   +12 more
doaj   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert   +4 more
wiley   +1 more source

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