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1
المؤلفون: Ellen Elinck, Jessie Theuns, Dirk Goossens, Barbara A. Pickut, Patrick Cras, Karen Nuytemans, Kristel Sleegers, Karin Peeters, Bram Meeus, L Debaene, Ellen Corsmit, Maria Mattheijssens, Christine Van Broeckhoven, Sebastiaan Engelborghs, Jurgen Del-Favero, David Crosiers, Peter Paul De Deyn
المصدر: Movement Disorders. 27:1451-1456
مصطلحات موضوعية: Genetics, Positional cloning, Guanosine triphosphate, Biology, Molecular biology, chemistry.chemical_compound, Exon, Neurology, chemistry, Transcription (biology), Regulatory sequence, Deletion mapping, Neurology (clinical), Copy-number variation, Gene
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2
المؤلفون: Karen Nuytemans, Bram Meeus, Dirk Goossens, Christine Van Broeckhoven, Sebastiaan Engelborghs, Jurgen Del-Favero, Peter Paul De Deyn, Marleen Van den Broeck, Philippe Pals, Nathalie Brouwers, Ellen Corsmit, Barbara A. Pickut, Jessie Theuns, Patrick Cras, David Crosiers
المساهمون: Clinical sciences, Neurology
المصدر: Human mutation
مصطلحات موضوعية: Ubiquitin-Protein Ligases, Protein-Serine-Threonine Kinases/genetics, DNA Mutational Analysis, Protein Deglycase DJ-1, Population, Gene Dosage, Case-control studies, Protein Serine-Threonine Kinases, Protein Kinases/genetics, Biology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, medicine.disease_cause, Belgium, Gene Frequency, Gene duplication, Genetics, medicine, Humans, alpha-Synuclein/genetics, Ubiquitin-Protein Ligases/genetics, Copy-number variation, Parkinson Disease/genetics, Mutation frequency, education, Belgium/epidemiology, Genetics (clinical), Oncogene Proteins, Medicine(all), education.field_of_study, Mutation, Intracellular Signaling Peptides and Proteins, PARK7, Parkinson Disease, Amplicon, LRRK2, Oncogene Proteins/genetics, Genetics, Population, alpha-Synuclein, Human medicine, mutation, Intracellular Signaling Peptides and Proteins/genetics, Protein Kinases
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3
المؤلفون: Christine Van Broeckhoven, Bram Meeus, Jessie Theuns
المصدر: Neurobiology of Aging. 31:1072-1074
مصطلحات موضوعية: Genetics, Aging, Parkinson's disease, General Neuroscience, Locus (genetics), Biology, medicine.disease, European descent, Genetic etiology, medicine, Missense mutation, Neurology (clinical), Geriatrics and Gerontology, Developmental Biology
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4
المؤلفون: Bram Meeus, Christine Van Broeckhoven, Jessie Theuns
المصدر: Archives of neurology
مصطلحات موضوعية: Lewy Body Disease, Alpha-synuclein, Dementia with Lewy bodies, Genetic heterogeneity, Presenilins, Brain, Disease, Heritability, medicine.disease, Amyloid beta-Protein Precursor, chemistry.chemical_compound, Arts and Humanities (miscellaneous), chemistry, Missing heritability problem, mental disorders, alpha-Synuclein, medicine, Humans, Dementia, Lewy Bodies, Neurology (clinical), Human medicine, Alzheimer's disease, Psychology, Neuroscience
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::907a1db1b7529c42917c1702cc8004fb
https://hdl.handle.net/10067/1018670151162165141 -
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المؤلفون: Eline Wauters, Ellen Corsmit, Rik Vandenberghe, Barbara A. Pickut, Ellen Elinck, David Crosiers, Patrick Cras, Jessie Theuns, Aline Verstraeten, Karin Peeters, Bram Meeus, Maria Mattheijssens, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter Paul De Deyn
المساهمون: Clinical sciences, Neurology, Faculteit Medische Wetenschappen/UMCG, Molecular Neuroscience and Ageing Research (MOLAR)
المصدر: Neurobiology of aging
Neurobiology of Aging, 33(8):ARTN 1844.e11. ELSEVIER SCIENCE INCمصطلحات موضوعية: Genetic Markers, Lewy Body Disease, Male, Aging, In silico, Population, Vesicular Transport Proteins, Disease, Biology, Polymorphism, Single Nucleotide, Vesicular Transport Proteins/genetics, Lewy Body Disease/epidemiology, Belgium, Risk Factors, Genetic Predisposition to Disease/epidemiology, medicine, Prevalence, Missense mutation, Humans, Genetic Predisposition to Disease, Genetic etiology, Copy-number variation, Genetic variability, education, Belgium/epidemiology, VPS35, Gene, Genetic Markers/genetics, Medicine(all), Genetics, Aged, 80 and over, education.field_of_study, Lewy body, General Neuroscience, Genetic Variation, Middle Aged, Polymorphism, Single Nucleotide/genetics, medicine.disease, Lewy body brain disorders, Genetic Variation/genetics, Human medicine, Neurology (clinical), Geriatrics and Gerontology, Developmental Biology
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6
المؤلفون: Jessie, Theuns, David, Crosiers, Luc, Debaene, Karen, Nuytemans, Bram, Meeus, Kristel, Sleegers, Dirk, Goossens, Ellen, Corsmit, Ellen, Elinck, Karin, Peeters, Maria, Mattheijssens, Barbara, Pickut, Jurgen, Del-Favero, Sebastiaan, Engelborghs, Peter Paul, De Deyn, Patrick, Cras, Christine, Van Broeckhoven
المصدر: Movement disorders : official journal of the Movement Disorder Society. 27(11)
مصطلحات موضوعية: Adult, Family Health, Male, Genetic Linkage, Dopamine Agents, Chromosome Mapping, Middle Aged, Levodopa, Dystonia, Young Adult, Belgium, Humans, Female, GTP Cyclohydrolase, Promoter Regions, Genetic, Genome-Wide Association Study, Sequence Deletion
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7
المؤلفون: Marleen Van den Broeck, Aline Verstraeten, Peter Paul De Deyn, Patrick Cras, Karin Peeters, Bram Meeus, Jessie Theuns, David Crosiers, Christine Van Broeckhoven, Ellen Corsmit, Maria Mattheijssens, Barbara A. Pickut, Ellen Elinck, Sebastiaan Engelborghs, Rik Vandenberghe
المساهمون: Clinical sciences, Neurology
المصدر: Neurobiology of aging
مصطلحات موضوعية: Adult, Lewy Body Disease, Male, Aging, DNA Copy Number Variations, DNA Copy Number Variations/genetics, Biology, behavioral disciplines and activities, Parkinson Disease/epidemiology, Lewy Body Disease/epidemiology, Cohort Studies, Amyloid beta-Protein Precursor, Genetic Predisposition to Disease/epidemiology, PSEN2, mental disorders, medicine, PSEN1, Dementia, Missense mutation, Humans, Point Mutation, Genetic Predisposition to Disease, Point Mutation/genetics, Copy-number variation, Prospective Studies, Amyloid beta-Protein Precursor/genetics, Aged, Medicine(all), Genetics, Aged, 80 and over, Dementia with Lewy bodies, General Neuroscience, Parkinson Disease, medicine.disease, LRRK2, nervous system diseases, Pedigree, Case-Control Studies, Female, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Alzheimer's disease, Developmental Biology
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8
المؤلفون: Karen Nuytemans, Christine Van Broeckhoven, Patrick Cras, Karin Peeters, Maria Mattheijssens, David Crosiers, Peter Paul De Deyn, Bram Meeus, Ellen Corsmit, Jessie Theuns, Barbara A. Pickut, Sebastiaan Engelborghs, Philippe Pals
المساهمون: Clinical sciences, Neurology
المصدر: Neurobiology of aging
مصطلحات موضوعية: Adult, Male, Aging, Carrier Proteins/genetics, Mutation/genetics, Population, DNA Mutational Analysis, Belgium/ethnology, Disease, Biology, medicine.disease_cause, Exon, Degenerative disease, Belgium, medicine, Missense mutation, Humans, Parkinson Disease/genetics, education, Gene, Aged, Genetics, Medicine(all), Mutation, education.field_of_study, General Neuroscience, Parkinson Disease, Middle Aged, medicine.disease, Chromosomal region, Female, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Carrier Proteins, Developmental Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d1a287e1298fe408fdcd34bf9e928e
https://biblio.vub.ac.be/vubir/gigyf2-has-no-major-role-in-parkinson-genetic-etiology-in-a-belgian-population(36329186-c1b4-473e-9a76-26eb5de0f0fa).html -
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المؤلفون: Jessie Theuns, Patrick Cras, Karen Nuytemans, Christine Van Broeckhoven, Berten Ceulemans, Bram Meeus, David Crosiers, Philippe Pals
المصدر: Parkinsonism and related disorders
مصطلحات موضوعية: Video recording, Pediatrics, medicine.medical_specialty, business.industry, Parkinsonism, medicine.disease, Frameshift mutation, Neurology, Kufor Rakeb syndrome, Rapid onset, medicine, Juvenile, Dementia, Dementia diagnosis, Neurology (clinical), Human medicine, Geriatrics and Gerontology, business
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10Comprehensive genetic and mutation analysis of familial dementia with Lewy bodies linked to 2q35-q36
المؤلفون: Peter Paul De Deyn, Ellen Corsmit, Maria Mattheijssens, Ellen Elinck, Bram Meeus, Jessie Theuns, Karen Nuytemans, Karin Peeters, Sebastiaan Engelborghs, David Crosiers, Christine Van Broeckhoven
المساهمون: Clinical sciences, Neurology
المصدر: Journal of Alzheimer's disease
مصطلحات موضوعية: Lewy Body Disease, Adult, Male, Candidate gene, DNA Copy Number Variations, Genotype, Genetic Linkage, DNA Mutational Analysis, Locus (genetics), Nerve Tissue Proteins, Disease, Biology, DNA Copy Number Variations/genetics, behavioral disciplines and activities, mental disorders, Databases, Genetic, medicine, Humans, Nerve Tissue Proteins/genetics, Copy-number variation, Chromosomes, Human, Pair 2/genetics, Gene, Aged, Genetics, Family Health, Medicine(all), Dementia with Lewy bodies, Genetic Linkage/physiology, General Neuroscience, Chromosome Mapping, General Medicine, Middle Aged, medicine.disease, Lewy Body Disease/genetics, nervous system diseases, Psychiatry and Mental health, Clinical Psychology, Tandem Repeat Sequences/genetics, nervous system, Tandem Repeat Sequences, Chromosomes, Human, Pair 2, Mutation testing, Female, Human medicine, Geriatrics and Gerontology, aged, 80 and over, Chromosome Mapping/methods
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461a718c6b98ae28b9641ea10a1a384a
https://doi.org/10.3233/jad-2010-1356
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