388 results match your criteria: "Manchester Centre for Clinical Neurosciences[Affiliation]"

A Rare Genetic Cause of Spastic Paraparesis.

Neurology

December 2024

From the Department of Neurology (S.B.), Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust; Department of Neuroradiology (R.S.), Walton Centre NHS Foundation Trust, Liverpool; North West Genomic Laboratory Hub (Liverpool) (A.S.), Manchester Centre for Genomic Medicine, Liverpool Women's Hospital; MRC Human Genetics Unit (Y.J.C.), Institute of Genetics and Cancer, University of Edinburgh, United Kingdom; Laboratory of Neurogenetics and Neuroinflammation (Y.J.C.), Imagine Institute, INSERM UMR1163, Paris, France; Department of Neurology (C.K.), Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust, Salford; and Division of Neuroscience (C.K.), Manchester Academic Health Science Centre, University of Manchester, United Kingdom.

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Alternatively activated macrophages are associated with faster growth rate in vestibular schwannoma.

Brain Commun

November 2024

Division of Neuroscience, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.

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Evolution of Robotics in Neurosurgery.

Asian J Neurosurg

December 2024

Neurosurgical Oncology Services, Department of Surgical oncology, Tata Memorial Centre, Mumbai, India.

Technology and neurosurgery have gone hand in hand since a long time. Technological development of robotics in neurosurgery over the last couple of decades has been rapid, yet it still has a long way to go before it becomes a "routine" element of the standard neurosurgical procedure. Apart from the obvious advantages they have over humans, that is, precision, consistency, endurance, and reproducibility, robots also provide additional freedom of movement beyond what is anatomically feasible for humans.

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Quantitative Imaging of Regional Cerebral Protein Synthesis in Clinical Alzheimer's Disease by [C]Leucine PET.

Mol Imaging Biol

December 2024

Faculty of Biology, Medicine and Health, School of Health Sciences, Division of Informatics, Imaging and Data Sciences, University of Manchester, Manchester, M13 9PL, UK.

Purpose: Protein synthesis is essential to maintain integrity and function of the human brain, and protein synthesis is associated specifically with the formation of long-term memory. Experimental and clinical observations indicate that this process is disturbed in Alzheimer's dementia and other neurodegenerative diseases. In-vivo investigation with positron emission tomography (PET) using [C]leucine provides a unique possibility to measure regional cerebral protein synthesis (rCPS) rates in human brain and to determine whether it is altered in Alzheimer's disease (AD), and thus may provide a target for future therapeutic interventions.

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Background: Angiogenesis and nascent blood vessel formation is thought to be important in cerebral arteriovenous malformation (cAVM) development and maintenance, of which little is known. Digital subtraction angiogram (DSA) features of angiogenesis in cAVMs are poorly described and the aim of this study was to describe the frequency of angiogenesis in patients who had a DSA showing a cAVM. We also sought to evaluate the intra- and inter-observer agreement of a diagnosis of angiogenesis and explore which angioarchitectural features were associated with angiogenesis.

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Subcortical Alterations in Newly Diagnosed Epilepsy and Associated Changes in Brain Connectivity and Cognition.

Hum Brain Mapp

November 2024

Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.

Article Synopsis
  • * This study involved a comparison between individuals with newly diagnosed focal epilepsy (NDfE) and healthy controls, using MRI and neuropsychological data to evaluate subcortical shape alterations and their impact on brain connectivity and cognitive function.
  • * Findings indicated significant inward deformation (localized atrophy) in the thalamus and pallidum of NDfE patients, and a correlation between reduced white matter integrity (measured by fractional anisotropy) and this shape deformation, suggesting links to neuropsychological outcomes.
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People with Huntington's disease (HD) often experience psychological difficulties linked with disease progression and the adjustment to living with a chronic condition, which are also frequently shared by their informal caregivers (e.g., partners).

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Background: The MSIS-29 measures the physical and psychological impact of MS.

Objective: The associations between MSIS-29 domains and demographic/clinical aspects were examined and trajectories analysed over time.

Methods: Data were collected in the Trajectories of Outcome in Neurological Conditions study for a diverse population of people with MS, with follow-up for up to 5 years.

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Attachment-informed mental healthcare systems as 'organisational caregivers': ideas for the future.

BJPsych Bull

October 2024

Department of Clinical Neuropsychology, Manchester Centre for Clinical Neurosciences, Salford Royal NHS Foundation Trust, Salford, UK.

Over the past 50 years, mental health services have evolved significantly, influenced by shifts in theoretical and practical approaches to mental disorders. Key among these changes are the biopsychosocial and recovery models, which highlight resilience and quality of life in treatment. However, traditional psychiatry has often struggled to embrace these changes because of reductionist perspectives that overlook psychosocial factors, resulting in fragmented care and reduced accessibility.

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  • - The ATTEST-2 trial evaluated if tenecteplase, a newer thrombolytic agent, is at least as effective as the standard alteplase within 4.5 hours of an acute ischaemic stroke by comparing outcomes like the modified Rankin Scale (mRS) at 90 days post-treatment.
  • - Conducted across 39 UK stroke centers, the study randomly assigned 1,777 eligible stroke patients to receive either tenecteplase or alteplase, focusing on their recovery outcomes and safety, including complications such as bleeding.
  • - Results showed that tenecteplase was non-inferior to alteplase regarding the distribution of mRS scores, but it did not
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  • This study explores apraxia across different pathological subtypes of frontotemporal lobar degeneration (FTLD), revealing its complexities and variations in symptoms and underlying mechanisms.
  • Out of 115 FTLD cases examined, 18 patients exhibited notable apraxia, with a higher prevalence linked to FTLD-tau pathologies, particularly in corticobasal degeneration (CBD) and Pick-type pathology.
  • The findings indicate that apraxia can present differently depending on the subtype, suggesting that it could have distinct cognitive and motor foundations that warrant further research.
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Neuroinflammation and blood-brain barrier breakdown in acute, clinical intracerebral hemorrhage.

J Cereb Blood Flow Metab

October 2024

Geoffrey Jefferson Brain Research Centre, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Neuroinflammation is a promising therapeutic target in intracerebral hemorrhage (ICH), characterized in the brain by microglial activation and blood-brain barrier (BBB) breakdown. In this study, 36 acute, spontaneous, supratentorial ICH patients underwent dynamic contrast-enhanced MRI to measure BBB permeability () 1-3 days post-onset and 16 returned for [C]()-PK11195 PET to quantify microglial activation (), 2-7 days post-onset. We first tested if these markers were increased and co-localized in the perihematomal brain and found that perihematomal and were increased vs.

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Article Synopsis
  • This study investigates the relationship between the percentage of prolapse to canal ratio (PCR) on MRI and cauda equina syndrome (CES) to establish a diagnostic benchmark.
  • Conducted on 61 patients who underwent emergency surgery due to lumbar issues, the research found that a higher PCR is associated with CES, particularly at the L4/5 level.
  • The optimal PCR value for diagnosing CES was identified as 66%, balancing sensitivity and specificity, which could help in deciding patient management in future cases.
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Utilising accessible and reproducible neurological assessments in clinical studies: Insights from use of the Neurological Impairment Scale in the multi-centre COVID-CNS study.

Clin Med (Lond)

September 2024

Infection Neuroscience Laboratory, Institute of Infection, Veterinary and Ecological Science, University of Liverpool, NIHR HPRU for Emerging and Zoonotic Infection, Liverpool, UK.

Reproducible and standardised neurological assessment scales are important in quantifying research outcomes. These scales are often performed by non-neurologists and/or non-clinicians and must be robust, quantifiable, reproducible and comparable to a neurologist's assessment. COVID-CNS is a multi-centre study which utilised the Neurological Impairment Scale (NIS) as a core assessment tool in studying neurological outcomes following COVID-19 infection.

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Article Synopsis
  • - The guidance for clinicians diagnosing cauda equina syndrome in England has improved, but lacks specific advice for patients with recent imaging showing no compression who return with new symptoms.
  • - This study analyzed case notes of 45 patients who sought care at an Emergency Department for cauda equina syndrome and underwent MRI, focusing on changes in symptoms from their first to subsequent visits.
  • - Results indicated that patients reporting an increase in symptoms were more likely to show cauda equina compression on their second MRI, suggesting that further imaging may be warranted even if previous scans were reassuring.
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Background: Severe dysphagia poses a significant challenge for clinicians regarding feeding tube choices, practices, and timing due to a lack of evidence-based guidance.

Objectives: To assess national clinical practices and opinions on gastrostomy use in patients with atypical parkinsonian syndromes (APS) across the UK.

Methods: Online survey was administered to clinicians and allied health professionals regarding availability of services, current use, perceived advantages, and problems associated with gastrostomy insertion.

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Autoantibodies and damage in patients with idiopathic inflammatory myopathies: A longitudinal multicenter study from the MYONET international network.

Semin Arthritis Rheum

October 2024

Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Theme Women's Health and Health Professionals, Medical Unit Allied Health Professionals, Karolinska University Hospital, Stockholm, Sweden.

Article Synopsis
  • The study aimed to analyze how damage from idiopathic inflammatory myopathies (IIM) changes over time and its relationship with different autoantibody subgroups using data from a large patient registry.
  • Researchers examined data from 757 patients classified by their autoantibody profiles and found that damage increased over the years, with varying rates depending on the type of autoantibody present.
  • Results indicated that patients with dermatomyositis-specific autoantibodies exhibited less damage per year, while those with anti-PM/Scl autoantibodies experienced greater damage, highlighting significant differences among the groups over a five-year follow-up.
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  • The study aimed to compare the occurrence of breakthrough COVID-19 infections (BIs) in fully vaccinated patients with systemic lupus erythematosus (SLE) against those with other rheumatic autoimmune diseases (rAIDs), non-rheumatic autoimmune diseases (nrAIDs), and healthy controls (HCs).
  • Results showed that 10.7% of SLE patients reported at least one BI, with frequencies similar to HCs and nrAID patients but higher than those with other rAIDs.
  • Overall, vaccinated SLE patients experienced comparable levels of COVID-19 infection frequency and severity as healthy individuals, with no significant association found between demographic factors or treatments and BIs in SLE patients.
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Objectives: People with multiple system atrophy (MSA) and their carers may have many concerns about their disease and the future. This survey of people with MSA and their carers aimed to increase understanding of end-of-life care and palliative care for this group.

Methods: A survey was undertaken by the MSA Trust of people living with MSA and carers of those with the condition between August and October 2022.

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Background: In recent times, clinical negligence claims against National Health Service hospitals have doubled, with 8% of claims being made due to "failure to warn/informed consent." This study aimed to assess the current compliance of the neurosurgical division within a large tertiary neuroscience center with the national legal framework and professional guidelines around the issue of surgical consent and to develop strategies to improve the consent process.

Methods: Electronic patient records (EPR) were accessed to collect demographic data and information regarding the surgical procedures.

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Diffuse neurofibroma of the head and neck are rare tumours which have unique clinical and radiological findings. Presurgical diagnosis is important as these lesions are usually highly vascular and pre-operative embolisation can reduce the risk of intra-operative haemorrhage. In this article we describe four cases; two which underwent pre-operative embolisation, which should aid the reader in successfully diagnosing this entity before biopsy/surgery.

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Article Synopsis
  • Late-onset Pompe Disease (LOPD) is a rare genetic disorder caused by a deficiency in an enzyme, leading to muscle damage and glycogen accumulation in cells.
  • This study used advanced techniques like single nuclei RNA sequencing to explore gene expression changes in muscle biopsies from LOPD patients compared to healthy controls, revealing significant metabolic shifts and inflammatory responses in affected fibers.
  • Findings suggest potential benefits of enzyme replacement therapy in restoring metabolic function, especially in healthy muscle fibers, emphasizing the importance of using modern methods to understand muscle disease at a cellular level.
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