Results 41 to 50 of about 30,141 (201)

ETF FTD library v2

, 2021
ETF FTD library ...
Nappa & Vegeta
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Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of MAPT Mutations: A Systematic Review

Frontiers in Bioscience-Landmark
Background: Microtubule-associated protein tau (MAPT) mutations are one of the main causes of genetic Frontotemporal dementia (FTD) and are characterised by high clinical heterogeneity.
Cristina Villa, Elisa Pellencin, Aurora Romeo, Giorgio Giaccone, Giacomina Rossi, Sara Prioni, Paola Caroppo   +6 more
doaj   +1 more source

Genetic Screening in Korean Patients with Frontotemporal Dementia Syndrome

Journal of Alzheimer's Disease Reports, 2022
Background: Frontotemporal dementia (FTD) syndrome is a genetically heterogeneous group of diseases. Pathogenic variants in the chromosome 9 open reading frame 72 ( C9orf72 ), microtubule-associated protein tau ( MAPT ), and progranulin ( GRN ) genes are
Eun-Joo Kim, Duk L. Na, Hee-Jin Kim, Kyung Won Park, Jae-Hong Lee, Jee Hoon Roh, Jay C. Kwon, Soo Jin Yoon, Na-Yeon Jung, Jee Hyang Jeong, Jae-Won Jang, Hee-Jin Kim, Kee Hyung Park, Seong Hye Choi, SangYun Kim, Young Ho Park, Byeong C. Kim, Young Chul Youn, Chang-Seok Ki, Seung Hyun Kim, Sang Won Seo, Young-Eun Kim   +21 more
doaj   +1 more source

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Scientific Reports, 2017
Frontotemporal dementia (FTD) is a neurodegenerative disorder predominantly affecting the frontal and temporal lobes. Genome-wide association studies (GWAS) on FTD identified only a few risk loci.
E. Taskesen, A. Mishra, S. van der Sluis, R. Ferrari, International FTD-Genomics Consortium, J. H. Veldink, M. A. van Es, A. B. Smit, D. Posthuma, Y. Pijnenburg   +9 more
doaj   +1 more source

Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort

, 2023
: OBJECTIVE To identify whether language impairment exists presymptomatically in genetic frontotemporal dementia (FTD), and if so, the key differences between the main genetic mutation groups.
Rademakers, Rosa, Masellis, Mario, Graff, Caroline, Bocchetta, Martina, Bouzigues, Arabella, Seelaar, Harro, Santana, Isabel, Tartaglia, Maria Carmela, Butler, Chris R., Convery, Rhian S., Le Ber, Isabelle, Greaves, Caroline V., Russell, Lucy L., Genetic FTD Initiative (GENFI), Laforce, Robert, Synofzik, Matthis, Galimberti, Daniela, Moreno, Fermin, Ducharme, Simon, Sorbi, Sandro, Finger, Elizabeth, Gerhard, Alex, Pasquier, Florence, Cash, David M., Levin, Johannes, MacDougall, Amy M., Rowe, James B., de Mendon\ue7a, Alexandre, Otto, Markus, Tiraboschi, Pietro, Samra, Kiran, Jiskoot, Lize, Sanchez-Valle, Raquel, Rohrer, Jonathan D., Bruffaerts, Rose, Borroni, Barbara, van Swieten, John C., Vandenberghe, Rik   +37 more
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Mortality in FTD: An Australian perspective

, 2021
THEME: Clinical manifestations TOPIC: Neuropsychiatry & beh neurology SUBTOPIC: Neuropsychiatry BACKGROUND: Survival duration in frontotemporal dementia (FTD) remains inconsistent, depending on the clinical phenotype with different risk factors ...
Velakoulis, D, Farrand, S, Kelso, W, Evans, AH, Walterfang, M, Eratne, D, Loi, SM, Chen, B, Tsoukra, P, Wibawa, P   +9 more
core   +1 more source

Progress in the concept development of the VNS—a beam-driven tokamak for component testing

Nuclear Fusion
The Volumetric Neutron Source (VNS) is a compact beam-driven tokamak with D–T plasma to generate a high neutron flux that will allow the testing and qualification of fusion nuclear components, in particular the breeding blanket.
C. Bachmann, M. Siccinio, G. Aiello, R. Ambrosino, J. Bajari, J. Boscary, S. Carusotti, V. Claps, A. Cufar, J. Elbez-Uzan, G. Federici, T. Franke, L. Giannini, C. Gliss, T. Haertl, C. Hopf, C. Luongo, I. Maione, D. Maisonnier, D. Marzullo, F. Maviglia, P. Marek, P. Mollicone, I. Moscato, R. Mozzillo, M. Muscat, I. Pagani, J.H. Park, P. Pereslavtsev, A. Quartararo, S. Renard, T. Steinbacher, A. Tarallo, E. Vallone, F. Vigano, S. Wiesen, C. Wu   +36 more
doaj   +1 more source

C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort

Annals of Clinical and Translational Neurology, 2023
Objective Frontotemporal dementia (FTD) encompasses a spectrum of neurodegenerative disorders, including behavioural variant FTD (bvFTD), semantic variant primary progressive aphasia (svPPA) and non‐fluent variant PPA (nfvPPA).
Yi Jayne Tan, Alisa C. W. Yong, Jia Nee Foo, Michelle M. Lian, Weng Khong Lim, Jacqueline Dominguez, Zhi Hui Fong, Kaavya Narasimhalu, Hui Jin Chiew, Kok Pin Ng, Simon K. S. Ting, Nagaendran Kandiah, Adeline S. L. Ng   +12 more
doaj   +1 more source

FTD and ALS: A Tale of Two Diseases [PDF]

Current Alzheimer Research, 2011
The first reports of disorders that in terms of cognitive and behavioral symptoms resemble frontotemporal dementia (FTD) and in terms of motor symptoms resemble amyotrophic lateral sclerosis (ALS) bring us back to the second half of the 1800s. Over the last 150 years, and especially in the last two decades, there has been growing evidence that FTD ...
R, Ferrari, D, Kapogiannis, E D, Huey, P, Momeni   +3 more
openaire   +2 more sources

Escripturação Mercantil [PDF]

, 1921
Livro destinado aos principiantes de escolas primária superiores e os que necessitam de noções de ...
FTD
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