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FIG4-Related Parkinsonism and the Particularities of the I41T Mutation: A Review of the Literature.
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- Genes, 2024, v. 15, n. 10, p. 1344, doi. 10.3390/genes15101344
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- Article
Pharmacological Treatments of Negative Symptoms in Schizophrenia—An Update.
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- Journal of Clinical Medicine, 2024, v. 13, n. 18, p. 5637, doi. 10.3390/jcm13185637
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- Article
Levodopa‐Carbidopa Intestinal Gel Reduces Dyskinesia in Parkinson's Disease in a Randomized Trial.
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- Movement Disorders, 2021, v. 36, n. 11, p. 2615, doi. 10.1002/mds.28703
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The Glutamate Dehydrogenase Pathway and Its Roles in Cell and Tissue Biology in Health and Disease.
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- Biology (2079-7737), 2017, v. 6, n. 1, p. 11, doi. 10.3390/biology6010011
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- Article
SORL1 mutation in a Greek family with Parkinson's disease and dementia.
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- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 10, p. 1961, doi. 10.1002/acn3.51433
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- Article
Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 336, doi. 10.1038/ejhg.2009.179
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- Article
Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts.
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- European Journal of Human Genetics, 2004, v. 12, n. 4, p. 301, doi. 10.1038/sj.ejhg.5201097
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- Article
Dyskinesia and Pain in Advanced Parkinson's Disease: Post Hoc Analysis from the Phase 3b, Open-Label, Randomized DYSCOVER Study.
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- Neurology & Therapy, 2024, v. 13, n. 2, p. 437, doi. 10.1007/s40120-024-00583-z
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- Article
Mitochondrial DNA polymorphisms and haplogroups in Parkinson’s disease and control individuals with a similar genetic background.
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- Journal of Human Genetics, 2008, v. 53, n. 4, p. 349, doi. 10.1007/s10038-008-0259-1
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- Article
The Christian Orthodox Church Fasting Diet Is Associated with Lower Levels of Depression and Anxiety and a Better Cognitive Performance in Middle Life.
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- Nutrients, 2021, v. 13, n. 2, p. 627, doi. 10.3390/nu13020627
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- Article
Transgenic Mice Carrying GLUD2 as a Tool for Studying the Expressional and the Functional Adaptation of this Positive Selected Gene in Human Brain Evolution.
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- Neurochemical Research, 2019, v. 44, n. 1, p. 154, doi. 10.1007/s11064-018-2546-3
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- Article
Widening Spectrum of Cellular and Subcellular Expression of Human GLUD1 and GLUD2 Glutamate Dehydrogenases Suggests Novel Functions.
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- Neurochemical Research, 2017, v. 42, n. 1, p. 92, doi. 10.1007/s11064-016-1986-x
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- Article
Heterogeneous Cellular Distribution of Glutamate Dehydrogenase in Brain and in Non-neural Tissues.
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- Neurochemical Research, 2014, v. 39, n. 3, p. 500, doi. 10.1007/s11064-013-1235-5
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- Article
Deregulation of glutamate dehydrogenase in human neurologic disorders.
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- Journal of Neuroscience Research, 2013, v. 91, n. 8, p. 1007, doi. 10.1002/jnr.23176
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Molecular basis of human glutamate dehydrogenase regulation under changing energy demands.
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- Journal of Neuroscience Research, 2005, v. 79, n. 1/2, p. 65
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- Article
Combining Device‐Aided Therapies in Parkinson's Disease: A Case Series and a Literature Review.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 5, p. 750, doi. 10.1002/mdc3.13228
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- Article
The Role of Glutamate Dehydrogenase in Mammalian Ammonia Metabolism.
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- Neurotoxicity Research, 2012, v. 21, n. 1, p. 117, doi. 10.1007/s12640-011-9285-4
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- Article
Evolution of GLUD2 Glutamate Dehydrogenase Allows Expression in Human Cortical Neurons.
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- Molecular Neurobiology, 2016, v. 53, n. 8, p. 5140, doi. 10.1007/s12035-015-9429-2
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- Article
Levodopa-aggravated lateral flexion of the neck and trunk as a delayed phenomenon of unilateral pallidotomy.
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- Movement Disorders, 2010, v. 25, n. 5, p. 655, doi. 10.1002/mds.22988
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- Article
Essential tremor in Parkinson's disease kindreds from a population of similar genetic background.
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- Movement Disorders, 2009, v. 24, n. 11, p. 1662, doi. 10.1002/mds.22655
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- Article
Evolution of Glutamate Metabolism via GLUD2 Enhances Lactate-Dependent Synaptic Plasticity and Complex Cognition.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5297, doi. 10.3390/ijms25105297
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- Article
Τhe Greek Variant in APP Gene: The Phenotypic Spectrum of APP Mutations.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12355, doi. 10.3390/ijms222212355
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- Article