Cargando…

Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study()

OBJECTIVE: Frontotemporal dementia (FTD) is characterized by behavioral disturbances and language problems. Familial forms can be caused by genetic defects in microtubule-associated protein tau (MAPT), progranulin (GRN), and C9orf72. In light of upcoming clinical trials with potential disease-modify...

Descripción completa

Detalles Bibliográficos
Autores principales:	Dopper, Elise G.P., Chalos, Vicky, Ghariq, Eidrees, den Heijer, Tom, Hafkemeijer, Anne, Jiskoot, Lize C., de Koning, Inge, Seelaar, Harro, van Minkelen, Rick, van Osch, Matthias J.P., Rombouts, Serge A.R.B., van Swieten, John C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2016
Materias:	Regular Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011170/ https://www.ncbi.nlm.nih.gov/pubmed/27625986 http://dx.doi.org/10.1016/j.nicl.2016.08.001

Ejemplares similares

Presymptomatic and early pathological features of MAPT-associated frontotemporal lobar degeneration
por: Giannini, Lucia AA, et al.
Publicado: (2023)

Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
por: Feis, Rogier A., et al.
Publicado: (2018)

Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
por: Feis, Rogier A., et al.
Publicado: (2019)

Longitudinal multimodal MRI as prognostic and diagnostic biomarker in presymptomatic familial frontotemporal dementia
por: Jiskoot, Lize C, et al.
Publicado: (2019)

Longitudinal cognitive biomarkers predicting symptom onset in presymptomatic frontotemporal dementia
por: Jiskoot, Lize C., et al.
Publicado: (2018)

Longitudinal Brain Atrophy Rates in Presymptomatic Carriers of Genetic Frontotemporal Dementia
por: Poos, Jackie M., et al.
Publicado: (2022)

[(18)F]Flortaucipir PET Across Various MAPT Mutations in Presymptomatic and Symptomatic Carriers
por: Wolters, Emma E., et al.
Publicado: (2021)

Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population
por: Simón-Sánchez, Javier, et al.
Publicado: (2009)

Cortical iron accumulation in MAPT ‐ and C9orf 72‐associated frontotemporal lobar degeneration
por: Giannini, Lucia A. A., et al.
Publicado: (2023)

Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia
por: Miedema, Suzanne S. M., et al.
Publicado: (2022)

Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia
por: Panman, Jessica L, et al.
Publicado: (2021)

Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation
por: Dopper, Elise G. P., et al.
Publicado: (2011)

Longitudinal changes in qualitative aspects of semantic fluency in presymptomatic and prodromal genetic frontotemporal dementia
por: Jiskoot, Lize C., et al.
Publicado: (2023)

Presymptomatic white matter integrity loss in familial frontotemporal dementia in the GENFI cohort: A cross‐sectional diffusion tensor imaging study
por: Jiskoot, Lize C., et al.
Publicado: (2018)

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?
por: Caroppo, Paola, et al.
Publicado: (2015)

Emotion recognition of morphed facial expressions in presymptomatic and symptomatic frontotemporal dementia, and Alzheimer’s dementia
por: Jiskoot, Lize C., et al.
Publicado: (2020)

Clinical Value of Longitudinal Serum Neurofilament Light Chain in Prodromal Genetic Frontotemporal Dementia
por: Giannini, Lucia A.A., et al.
Publicado: (2023)

Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
por: Ghariq, Eidrees, et al.
Publicado: (2011)

White-matter abnormalities in presymptomatic GRN and C9orf72 mutation carriers
por: Lee, Hyunwoo, et al.
Publicado: (2022)

Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration
por: Giannini, Lucia A. A., et al.
Publicado: (2022)

Correction to: Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration
por: Giannini, Lucia A. A., et al.
Publicado: (2023)

Resting state functional connectivity differences between behavioral variant frontotemporal dementia and Alzheimer's disease
por: Hafkemeijer, Anne, et al.
Publicado: (2015)

Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations
por: Bouzigues, Arabella, et al.
Publicado: (2022)

Bias Introduced by Multiple Head Coils in MRI Research: An 8 Channel and 32 Channel Coil Comparison
por: Panman, Jessica L., et al.
Publicado: (2019)

The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics
por: Moreno, Fermin, et al.
Publicado: (2017)

Joint assessment of white matter integrity, cortical and subcortical atrophy to distinguish AD from behavioral variant FTD: A two-center study
por: Möller, Christiane, et al.
Publicado: (2015)

Progranulin Levels in Plasma and Cerebrospinal Fluid in Granulin Mutation Carriers
por: Meeter, Lieke H.H., et al.
Publicado: (2016)

Early anterior cingulate involvement is seen in presymptomatic MAPT P301L mutation carriers
por: Clarke, Mica T. M., et al.
Publicado: (2021)

Cerebrovascular reactivity in retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
por: Hoogeveen, Evelien S, et al.
Publicado: (2020)

Characterizing the Clinical Features and Atrophy Patterns of MAPT-Related Frontotemporal Dementia With Disease Progression Modeling
por: Young, Alexandra L., et al.
Publicado: (2021)

Total Bolus Extraction Method Improves Arterial Image Quality in Dynamic CTAs Derived from Whole-Brain CTP Data
por: Ghariq, Elyas, et al.
Publicado: (2014)

Mindfulness-Based Stress Reduction in Pre-symptomatic Genetic Frontotemporal Dementia: A Pilot Study
por: Poos, Jackie M., et al.
Publicado: (2022)

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
por: Guven, Gamze, et al.
Publicado: (2016)

Early grey matter changes in structural covariance networks in Huntington's disease
por: Coppen, Emma M., et al.
Publicado: (2016)

Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic Variants
por: Staffaroni, Adam M., et al.
Publicado: (2020)

Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort
por: Bocchetta, Martina, et al.
Publicado: (2023)

Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders
por: Jiskoot, Lize C., et al.
Publicado: (2023)

A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
por: Bergström, Sofia, et al.
Publicado: (2021)

Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease
por: Sassi, Celeste, et al.
Publicado: (2014)

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
por: Seelaar, Harro, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_ddqk8d5s6utm1oo45f25g1a6cf