Results 1 to 10 of about 30,141 (201)

Co-morbid seizures in frontotemporal dementia: MRI and PET correlations [PDF]

Epilepsy & Behavior Reports
Seizures are common in frontotemporal dementia (FTD). MRI and PET findings may provide valuable diagnostic insights for FTD patients with seizures, but are understudied.
Syeda Amrah Hashmi, Jaideep Kapur, Mark Quigg, Anelyssa D’Abreu, Carol Manning, Prachi Parikh, Ifrah Zawar   +6 more
doaj   +2 more sources

The converging roles of sequestosome-1/p62 in the molecular pathways of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)

Neurobiology of Disease, 2022
Investigations into the pathogenetic mechanisms underlying amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have provided significant insight into the disease.
Jennilee M Davidson, Roger S Chung, Albert Lee   +2 more
exaly   +3 more sources

The Pathology of field Training detachment in the Air Force of the Islamic Republic of Iran [PDF]

علوم و فنون نظامی, 2020
The purpose of the present study was to determine the pathology of FTD Air Force training of the Islamic Republic of Iran Army using the Tricycle model.
Ali Shakibarad, Hossain Akbari
doaj   +1 more source

Inducible expression of human C9ORF72 36× G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice

Disease Models & Mechanisms, 2021
The hexanucleotide G4C2 repeat expansion in the first intron of the C9ORF72 gene accounts for the majority of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) cases.
Fréderike W. Riemslagh, Esmay C. van der Toorn, Rob F. M. Verhagen, Alex Maas, Laurens W. J. Bosman, Renate K. Hukema, Rob Willemsen   +6 more
doaj   +1 more source

Behavioural Variant Frontotemporal Dementia with Bilateral Insular Hypometabolism: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Fronto-Temporal Dementia (FTD) is a cluster of syndromes, characterized by progressive deterioration of cognition, language and/or behavioural changes associated with degeneration of the frontal and temporal lobes.
Ananya Mahapatra, Mamta Sood, Roshan Bhad, Manjari Tripathi   +3 more
doaj   +1 more source

Differences and similarities between familial and sporadic frontotemporal dementia: An Italian single‐center cohort study

Alzheimer’s & Dementia: Translational Research & Clinical Interventions, 2022
Introduction The possibility to generalize our understandings on treatments and assessments to both familial frontotemporal dementia (f‐FTD) and sporadic FTD (s‐FTD) is a fundamental perspective for the near future, considering the constant advancement ...
Alberto Benussi, Ilenia Libri, Enrico Premi, Antonella Alberici, Valentina Cantoni, Yasmine Gadola, Jasmine Rivolta, Marta Pengo, Stefano Gazzina, Vince D. Calhoun, Roberto Gasparotti, Henrik Zetterberg, Nicholas J. Ashton, Kaj Blennow, Alessandro Padovani, Barbara Borroni   +15 more
doaj   +1 more source

Altered plasma protein profiles in genetic FTD – a GENFI study

Molecular Neurodegeneration, 2023
Background Plasma biomarkers reflecting the pathology of frontotemporal dementia would add significant value to clinical practice, to the design and implementation of treatment trials as well as our understanding of disease mechanisms.
Abbe Ullgren, Linn Öijerstedt, Jennie Olofsson, Sofia Bergström, Julia Remnestål, John C. van Swieten, Lize C. Jiskoot, Harro Seelaar, Barbara Borroni, Raquel Sanchez-Valle, Fermin Moreno, Robert Laforce, Matthis Synofzik, Daniela Galimberti, James B. Rowe, Mario Masellis, Maria Carmela Tartaglia, Elizabeth Finger, Rik Vandenberghe, Alexandre de Mendonça, Pietro Tirabosch, Isabel Santana, Simon Ducharme, Chris R. Butler, Alexander Gerhard, Markus Otto, Arabella Bouzigues, Lucy Russell, Imogen J. Swift, Aitana Sogorb-Esteve, Carolin Heller, Jonathan D. Rohrer, Anna Månberg, Peter Nilsson, Caroline Graff, on behalf of the Genetic Frontotemporal Dementia Initiative (GENFI)   +35 more
doaj   +1 more source

Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations

Acta Neuropathologica Communications, 2023
Heterozygous mutations in the GRN gene and hexanucleotide repeat expansions in C9orf72 are the two most common genetic causes of Frontotemporal Dementia (FTD) with TDP-43 protein inclusions. The triggers for neurodegeneration in FTD with GRN (FTD-GRN) or
Oana C. Marian, Jonathan D. Teo, Jun Yup Lee, Huitong Song, John B. Kwok, Ramon Landin-Romero, Glenda Halliday, Anthony S. Don   +7 more
doaj   +1 more source

ANXA11 mutations are associated with amyotrophic lateral sclerosis–frontotemporal dementia

Frontiers in Neurology, 2022
BackgroundThe Annexin A11 (ANXA11) gene has been newly identified as a causative gene of amyotrophic lateral sclerosis (ALS) with or without frontotemporal dementia (FTD).
Yu Wang, Xiaohui Duan, Xiao Zhou, Renbin Wang, Xiangfei Zhang, Zhenhua Cao, Xiaoxia Wang, Zhi Zhou, Yu Sun, Dantao Peng   +9 more
doaj   +1 more source

Prosopagnosia, Other Specific Cognitive Deficits, and Behavioral Symptoms: Comparison between Right Temporal and Behavioral Variant of Frontotemporal Dementia

Vision, 2022
Right temporal variant of frontotemporal dementia (rtv-FTD) represents an uncommon and recently described frontotemporal dementia (FTD) entity presenting with symptoms in many ways comparable to those of the frontal or behavioral variant of FTD (bv-FTD).
Christos Koros, Ion Beratis, Stavroula Matsi, Anastasia Bougea, Anastasios Bonakis, Ioannis Papatriantafyllou, Efthalia Angelopoulou, Elisabeth Kapaki, Leonidas Stefanis, Sokratis G. Papageorgiou   +9 more
doaj   +1 more source