Julie S. Snowden

ORCID: 0000-0002-3976-4310
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About
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Research Areas
  • Alzheimer's disease research and treatments
  • Amyotrophic Lateral Sclerosis Research
  • Dementia and Cognitive Impairment Research
  • Parkinson's Disease Mechanisms and Treatments
  • Neurobiology of Language and Bilingualism
  • Genetic Neurodegenerative Diseases
  • Neurological diseases and metabolism
  • Memory and Neural Mechanisms
  • Cerebrovascular and genetic disorders
  • Neurological disorders and treatments
  • Cholinesterase and Neurodegenerative Diseases
  • Prion Diseases and Protein Misfolding
  • Neurogenetic and Muscular Disorders Research
  • Mitochondrial Function and Pathology
  • Medical Imaging Techniques and Applications
  • S100 Proteins and Annexins
  • Neurological Disorders and Treatments
  • Language Development and Disorders
  • Bioinformatics and Genomic Networks
  • Neurological and metabolic disorders
  • Genetics and Neurodevelopmental Disorders
  • Neurological Disease Mechanisms and Treatments
  • Genomics and Rare Diseases
  • Reading and Literacy Development
  • RNA regulation and disease

University of Manchester
2014-2024

Salford Royal NHS Foundation Trust
2015-2024

Salford Royal Hospital
2013-2024

University of Salford
2002-2024

Istituto Universitario di Studi Superiori di Pavia
2022

University of Duisburg-Essen
2021

Manchester Academic Health Science Centre
2007-2018

Health Sciences Centre
2013-2016

Institute of Mental Health
2016

Greater Manchester STEM Centre
2001-2013

Presents case reports of a 67‐yr‐old man and 2 women (aged 60 66 yrs) with primary cerebral atrophy in whom progressive breakdown language visual perception are attributed to loss semantic information. This form dementia is distinct from that Alzheimer′s disease assumed represent circumscribed emphasis pathology temporal rather than frontal regions the brain.

10.1155/1989/124043 article EN cc-by Behavioural Neurology 1989-01-01

To test predictions that frontotemporal dementia and semantic give rise to distinct patterns of behavioural change.An informant based semistructured interview, covering the domains basic social emotions, personal behaviour, sensory eating oral repetitive behaviours, rituals, compulsions, was administered carers 41 patients with apathetic (FTD-A) disinhibited (FTD-D) forms dementia.Consistent prediction, emotional changes differentiated FTD from dementia. Whereas lack response pervasive in...

10.1136/jnnp.70.3.323 article EN Journal of Neurology Neurosurgery & Psychiatry 2001-03-01

A significant proportion of patients with presenile dementia due to primary cerebral atrophy do not have Alzheimer9s disease. One form non-Alzheimer may be designated as frontal lobe type (DFT), on the basis a characteristic neuropsychological picture suggestive disorder, confirmed by findings single photon emission tomography. The case histories seven exemplify disorder: presentation social misconduct and personality change, unconcern disinhibition, in presence physical well-being few...

10.1136/jnnp.51.3.353 article EN Journal of Neurology Neurosurgery & Psychiatry 1988-03-01

The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as cause chromosome 9-linked frontotemporal dementia and motor neuron disease offers opportunity for greater understanding relationship between these disorders other clinical forms lobar degeneration.In this study, we screened cohort 398 patients with dementia, progressive non-fluent aphasia, semantic or mixture syndromes mutations gene.Motor was present 55 (14%).We identified 32 mutations, representing 8% cohort.The...

10.1093/brain/awr355 article EN Brain 2012-02-02

Four patients are described, in whom a profound and rapidly progressive dementia occurred association with clinical features of motor neuron disease. The pattern indicated impaired frontal lobe function, confirmed by reduced tracer uptake the lobes on single photon emission computed tomography (SPECT). Pathological examination brains two revealed frontal-lobe atrophy, mild gliosis spongiform change. spinal cord changes were consistent picture pathological findings resembled those type...

10.1136/jnnp.53.1.23 article EN Journal of Neurology Neurosurgery & Psychiatry 1990-01-01

Semantic dementia is a focal clinical syndrome, resulting from degeneration of the temporal lobes and characterized by progressive loss conceptual knowledge about world. Because highly circumscribed nature disorder it natural model for improving understanding how semantic information cerebrally represented. There currently lack consensus. One view proposes existence modality specific meaning systems, in which visual verbal are stored separately. An opposing assumes that represented unitary,...

10.1093/brain/awh099 article EN Brain 2004-01-14

Multiple neurotransmitter deficits found in recent autopsy studies of patients with Alzheimer's disease may militate against the success "simple cholinergic replacement" as treatment. To study acetylcholine synthesis, we measured incorporation radiolabeled glucose into transmitter temporal-cortex specimens obtained at diagnostic craniotomy 17 young disease. Synthesis was significantly correlated cognitive impairment. These results are consistent view that deficit presynaptic system is a...

10.1056/nejm198507043130102 article EN New England Journal of Medicine 1985-07-04

We have investigated the extent and pattern of immunostaining for ubiquitin protein (UBQ) in 60 patients with frontotemporal lobar degeneration (FTLD) ubiquitin-positive, tau-negative inclusions (FTLD-U), 37 whom were ascertained Manchester UK 23 Newcastle-Upon-Tyne, UK. There three distinct histological patterns according to form distribution UBQ pathology. Histological type 1 was present 19 (32%) characterised by presence a moderate number, or numerous, immunoreactive neurites...

10.1007/s00401-006-0138-9 article EN cc-by-nc Acta Neuropathologica 2006-09-26
Katrina Moore Jennifer Nicholas Murray Grossman Corey T. McMillan David J. Irwin and 95 more Lauren Massimo Vivianna M Van Deerlin Jason D. Warren Nick C. Fox Martin N. Rossor Simon Mead Martina Bocchetta Bradley F. Boeve David S. Knopman Neill R. Graff‐Radford Leah K. Forsberg Rosa Rademakers Zbigniew K. Wszołek John C. van Swieten Lize C. Jiskoot Lieke Meeter Elise G.P. Dopper Janne M. Papma Julie S. Snowden Jennifer A. Saxon Matthew Jones Stuart Pickering‐Brown Isabelle Le Ber Agnès Camuzat Alexis Brice Paola Caroppo Roberta Ghidoni Michela Pievani Luisa Benussi Giuliano Binetti Bradford C. Dickerson Diane Lucente Samantha Krivensky Caroline Graff Linn Öijerstedt Marie Fallström Håkan Thonberg Nupur Ghoshal John C. Morris Barbara Borroni Alberto Benussi Alessandro Padovani Daniela Galimberti Elio Scarpini Giorgio Fumagalli Ian R. Mackenzie Ging‐Yuek Robin Hsiung Pheth Sengdy Adam L. Boxer Howie Rosen Joanne Taylor Matthis Synofzik Carlo Wilke Patricia Sulzer John R. Hodges Glenda M. Halliday John B. Kwok Raquel Sánchez‐Valle Albert Lladó Sergi Borrego‐Écija Isabel Santana Maria Rosário Almeida Miguel Tábuas‐Pereira Fermín Moreno Myriam Barandiarán Begoña Indakoetxea Johannes Levin Adrian Danek James B. Rowe Thomas Cope Markus Otto Sarah Anderl‐Straub Alexandre de Mendonça Carolina Maruta Mario Masellis Sandra E. Black Philippe Couratier Géraldine Lautrette Edward D. Huey Sandro Sorbi Benedetta Nacmias Robert Laforce Marie-Pier L Tremblay Rik Vandenberghe Philip Van Damme Emily Rogalskı Sandra Weıntraub Alexander Gerhard Chiadi U. Onyike Simon Ducharme Sokratis G. Papageorgiou Adeline Su Lyn Ng Amy Brodtmann Elizabeth Finger Rita Guerreiro

10.1016/s1474-4422(19)30394-1 article EN The Lancet Neurology 2019-12-04

Accuracy of clinical diagnosis dementia is increasingly important for therapeutic and scientific investigations. In this study, we examine diagnostic accuracy in a consecutive series 228 patients referred to specialist early-onset clinic, whose brains were subsequently examined at post-mortem. Diagnosis was based on structured history, neurological examination neuropsychological assessment, with emphasis qualitative as well quantitative aspects performance. Neuroimaging provided support but...

10.1093/brain/awr189 article EN Brain 2011-08-11

Objective: We aimed to determine the extent which patients with progressive language impairment conform 2011 primary aphasia (PPA) classification and examine clinicopathologic correlations within PPA variants. Methods: Sixty-two consecutive pathologically confirmed dementia who presented clinically were identified. Patients insufficient clinical information excluded. classifications applied anonymized data taken from patients' initial assessment by raters blinded pathologic diagnosis....

10.1212/01.wnl.0000436070.28137.7b article EN Neurology 2013-10-19
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