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KSII Transactions on Internet and Information Systems (TIIS), ISSN 1976-7277, 2013, Volume 7, Issue 2, pp. 366 - 385
In this paper, we propose a compressed sensing (CS) based Wyner-Ziv (WZ) codec using motion-aligned auto regressive model (MAAR) based side information (SI)... 
Wyner-Ziv codec | Compressed sensing | motion-aligned auto regressive model | side information
Journal Article
Journal of China Institute of Communications, ISSN 1000-436X, 11/2010, Volume 31, Issue 11, pp. 41 - 48
A novel Wyner-Ziv spatial scalable video coding using compressive sensing was proposed for the ubiquitous networks. At the encoder, both the base layer and... 
Networks | Coding | China | Entropy | Robustness | Detection | Video signals | Encoders
Journal Article
Parkinsonism & Related Disorders, ISSN 1353-8020, 11/2019
Journal Article
Movement Disorders, ISSN 0885-3185, 10/2019, Volume 34, Issue 10, pp. 1581 - 1582
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 08/2015, Volume 60, Issue 8, pp. 461 - 462
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2017, Volume 81, Issue 2, pp. 325 - 326
Journal Article
Current Neurology and Neuroscience Reports, ISSN 1528-4042, 8/2018, Volume 18, Issue 8, pp. 1 - 10
GBA mutations are the most common known genetic cause of Parkinson’s disease (PD). Its biological pathway may be important in idiopathic PD, since activity of... 
Neurology | Neurosciences | Glucocerebrosidase | Medicine & Public Health | Synucleinopathy | Genetics | Parkinson’s disease | Genetic counseling | Mutation
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 08/2015, Volume 60, Issue 8, pp. 461 - 462
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 11, pp. 1118 - 1118
  Recently, based on accumulating data from various models, researchers hypothesised that calpain 1 and calpain 2 have opposing roles in the brain, including... 
Neurology | ALZHEIMERS-DISEASE | CLINICAL NEUROLOGY | Calpain | Health aspects | Studies | Traumatic brain injury | Neurodegeneration | Ataxia | Mutation | Paralysis | Alzheimers disease
Journal Article
Dianzi Xuebao (Acta Electronica Sinica), ISSN 0372-2112, 10/2007, Volume 35, Issue 10, pp. 2014 - 2018
Distributed video coding (DVC) is a new video compression paradigm based on two key information theories: Slepi-an-Wolf and Wyner-Ziv theorems, and it has the... 
Journal Article
Movement Disorders, ISSN 0885-3185, 06/2019, Volume 34, Issue 6, pp. 866 - 875
Background Increasing evidence supports an extensive and complex genetic contribution to PD. Previous genome‐wide association studies (GWAS) have shed light on... 
Parkinson's disease | age at onset | TMEM175 | GBA | SNCA | METAANALYSIS | GBA MUTATIONS | CLINICAL NEUROLOGY | PENETRANCE | LONGEVITY | RISK LOCI | GLUCOCEREBROSIDASE | STATISTICAL POWER | APOE | EXPRESSION | EFFICIENT | Genetic variability | Neurodegenerative diseases | Alleles | Genomes | Heritability | Gene loci | Genetic diversity | Synuclein | Age | Movement disorders
Journal Article
Jisuanji Gongcheng yu Yingyong (Computer Engineering and Applications), ISSN 1002-8331, 07/2007, Volume 42, Issue 19, pp. 53 - 56
The distributed video coding theory and the Wyner-Ziv video coding , which is a kind of typical distributed video coding scheme , are introduced at first.Then... 
Journal Article
Neurology, ISSN 0028-3878, 11/2016, Volume 87, Issue 20, pp. 2173 - 2173
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 11/2019
Journal Article
by Schormair, Barbara and Zhao, Chen and Bell, Steven and Bell, Robert K and Tilch, Erik and Salminen, Aaro V and Pütz, Benno and Dauvilliers, Yves and Stefani, Ambra and Högl, Birgit and Poewe, Werner and Kemlink, David and Sonka, Karel and Bachmann, Cornelius G and Paulus, Walter and Trenkwalder, Claudia and Oertel, Wolfgang H and Hornyak, Magdolna and Teder-Laving, Maris and Metspalu, Andres and Hadjigeorgiou, Georgios M and Polo, Olli and Fietze, Ingo and Ross, Owen A and Wszolek, Zbigniew and Butterworth, Adam S and Soranzo, Nicole and Ouwehand, Willem H and Roberts, David J and Danesh, John and Allen, Richard P and Earley, Christopher J and Ondo, William G and Xiong, Lan and Montplaisir, Jacques and Gan-Or, Ziv and Perola, Markus and Vodicka, Pavel and Dina, Christian and Franke, Andre and Tittmann, Lukas and Stewart, Alexandre F R and Shah, Svati H and Gieger, Christian and Peters, Annette and Rouleau, Guy A and Berger, Klaus and Oexle, Konrad and Di Angelantonio, Emanuele and Hinds, David A and Müller-Myhsok, Bertram and Winkelmann, Juliane and Balkau, B and Ducimetière, P and Eschwège, E and Rancière, F and Alhenc-Gelas, F and Gallois, Y and Girault, A and Fumeron, F and Marre, M and Roussel, R and Bonnet, F and Bonnefond, A and Cauchi, S and Froguel, P and Cogneau, J and Born, C and Caces, E and Cailleau, M and Lantieri, O and Moreau, JG and Rakotozafy, F and Tichet, J and Vol, S and Agee, Michelle and Alipanahi, Babak and Auton, Adam and Bryc, Katarzyna and Elson, Sarah L and Fontanillas, Pierre and Furlotte, Nicholas A and Hromatka, Bethann S and Huber, Karen E and Kleinman, Aaron and Litterman, Nadia K and McIntyre, Matthew H and Mountain, Joanna L and Northover, Carrie AM and Pitts, Steven J and Sathirapongsasuti, J Fah and Sazonova, Olga V and Shelton, Janie F and Shringarpure, Suyash and Tian, Chao and Tung, Joyce Y and Vacic, Vladimir and Wilson, Catherine H and Collaboration 23andMe Res Team and DESIR Study Grp and DESIR study group and 23andMe Research Team
The Lancet Neurology, ISSN 1474-4422, 11/2017, Volume 16, Issue 11, pp. 898 - 907
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 09/2019, Volume 28, Issue 17, pp. 2811 - 2825
Abstract Mutations in Parkin (PARK2), which encodes an E3 ubiquitin ligase implicated in mitophagy, are the most common cause of early-onset Parkinson’s... 
Journal Article
Neurology, ISSN 0028-3878, 03/2015, Volume 84, Issue 9, pp. 880 - 887
OBJECTIVE:To better define the genotype-phenotype correlations between the type of GBA (glucosidase, beta, acid) mutation, severe or mild, and the risk and age... 
POPULATION | CONFER | RISK-FACTOR | GLUCOCEREBROSIDASE GENE-MUTATIONS | EARLY-ONSET | CHINESE | HIGH SUSCEPTIBILITY | ASSOCIATION | CLINICAL NEUROLOGY | GAUCHER-DISEASE | L444P MUTATION | Severity of Illness Index | Glucosylceramidase - genetics | Humans | Middle Aged | Parkinson Disease - diagnosis | Female | Male | Aged | Parkinson Disease - genetics | Mutation - genetics | Jews - genetics | Cohort Studies | 165
Journal Article
JOURNAL OF HUMAN GENETICS, ISSN 1434-5161, 11/2019, Volume 64, Issue 11, pp. 1145 - 1151
More than 80 known or suspected genes/loci have been reported to be involved in hereditary spastic paraplegia (HSP). Genetic and clinical overlap have been... 
DOMINANT | MUTATIONS | GENE | ALPHA-II-SPECTRIN | REPEATS | GENETICS & HEREDITY
Journal Article
Neurology, ISSN 0028-3878, 11/2016, Volume 87, Issue 20, pp. 2173 - 2173
Journal Article
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