نتائج البحث - "Marleen Van den Broeck"

المساهمون: Frisoni, Giovanni, Repositório da Universidade de Lisboa, BELNEU Consortium, EU EOD Consortium, Physiotherapy, Human Physiology and Anatomy, Clinical sciences, Neurology, Pathologic Biochemistry and Physiology

المصدر: NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of Aging, Vol. 66 (2018) pp. 181.e3-181.e10
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Neurobiology of aging

مصطلحات موضوعية: 0301 basic medicine, Nonsynonymous substitution, Male, Aging, Geriatrics & Gerontology, Granulin, AMYOTROPHIC-LATERAL-SCLEROSIS, Cohort Studies, 0302 clinical medicine, Progranulins, Belgium, Medicine(all), Genetics, PLASMA, General Neuroscience, Adaptor Proteins, Vesicular Transport/chemistry, Middle Aged, Europe, Genetic Variation/genetics, Intercellular Signaling Peptides and Proteins, Female, Frontotemporal dementia, Genetic association, Rare variants, Sortilin, Life Sciences & Biomedicine, Cohort study, Protein Binding, Risk, Neuroscience(all), DIAGNOSTIC-CRITERIA, Clinical Neurology, PROGRANULIN LEVELS, C9ORF72, Biology, 03 medical and health sciences, Protein Domains, Genetic variation, mental disorders, medicine, Dementia, Humans, BELGIAN COHORT, Adaptor Proteins, Vesicular Transport/chemistry/genetics, LOBAR DEGENERATION, Gene, Genetic Association Studies, Aged, Science & Technology, HEXANUCLEOTIDE REPEAT, Binding Sites, MUTATIONS, Neurosciences, Genetic Variation, medicine.disease, Ageing, Adaptor Proteins, Vesicular Transport, 030104 developmental biology, ddc:618.97, Human medicine, Neurology (clinical), Neurosciences & Neurology, Geriatrics and Gerontology, 030217 neurology & neurosurgery, Developmental Biology

وصف الملف: Print-Electronic; application/pdf; pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae5d3acf43be2e53ceda38dda5b8884
https://hdl.handle.net/11379/576260

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7

Clinical variability and onset age modifiers in an extended Belgian GRN founder family

المساهمون: Neurology, Neuroprotection & Neuromodulation, Clinical sciences, Medicine and Pharmacy academic/administration, Belgian Neurology (BELNEU) Consortium, Wauters, Eline, Van Mossevelde, Sara, Sleegers, Kristel, van der Zee, Julie, Engelborghs, Sebastiaan, Sieben, Anne, Vandenberghe, Rik, PHILTJENS, Stephanie, Van den Broeck, Marleen, Peeters, Karin, Cuijt, Ivy, De Coster, Wouter, Van Langenhove, Tim, Santens, Patrick, Ivanoiu, Adrian, Cras, Patrick, De Bleecker, Jan L., Versijpt, Jan, Crols, Roeland, DE KLIPPEL, Nina, Martin, Jean-Jacques, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine

المصدر: NEUROBIOLOGY OF AGING
Neurobiology of aging

مصطلحات موضوعية: 0301 basic medicine, Clinical heterogeneity, Male, Aging, Geriatrics & Gerontology, Granulin, AMYOTROPHIC-LATERAL-SCLEROSIS, 0302 clinical medicine, Progranulins, Belgium, Loss of Function Mutation, Medicine and Health Sciences, Age of Onset, Exome, Genetics, Aged, 80 and over, Dimethylhydrazines, medicine.diagnostic_test, DEMENTIA, General Neuroscience, Frontotemporal lobar degeneration, Middle Aged, Pedigree, modifiers, ALZHEIMERS-DISEASE, Frontotemporal Dementia, Mutation (genetic algorithm), Intercellular Signaling Peptides and Proteins, Female, Life Sciences & Biomedicine, Frontotemporal dementia, GRN, Adult, Neuroscience(all), DIAGNOSTIC-CRITERIA, Clinical Neurology, PROGRANULIN LEVELS, MUTATION CARRIERS, Biology, Progressive supranuclear palsy, 03 medical and health sciences, medicine, Dementia, Humans, GRANULIN MUTATION CARRIERS, Genetic Association Studies, Genetic testing, Aged, FRONTOTEMPORAL LOBAR DEGENERATION, Science & Technology, Founder pedigree, HEXANUCLEOTIDE REPEAT, LINKAGE ANALYSIS, TARDBP MUTATIONS, Modifiers, Neurosciences, PROGRESSIVE SUPRANUCLEAR PALSY, medicine.disease, Ageing, 030104 developmental biology, TAU-GENE, Neurosciences & Neurology, Human medicine, Neurology (clinical), Geriatrics and Gerontology, Propionates, 030217 neurology & neurosurgery, Developmental Biology, Follow-Up Studies

وصف الملف: application/pdf; pdf; Print-Electronic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::764e5e2422d37d9c03d75bec57cccb97
https://pubmed.ncbi.nlm.nih.gov/29653316

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8

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

المؤلفون: Sebastiaan Engelborghs, Steven Vermeulen, Mathieu Vandenbulcke, Arne De Roeck, Tobi Van den Bossche, Rik Vandenberghe, Marleen Van den Broeck, Anne Sieben, Jean-Jacques Martin, Annelies Laureys, Peter Paul De Deyn, Caroline Van Cauwenberghe, Patrick Cras, Kristel Sleegers, Maria Mattheijssens, Karin Peeters, Christine Van Broeckhoven, Elise Cuyvers

المساهمون: Clinical sciences, Neurology, Physiotherapy, Human Physiology and Anatomy, Pathologic Biochemistry and Physiology, Molecular Neuroscience and Ageing Research (MOLAR)

المصدر: Neurology
NEUROLOGY
Neurology, 86(23), 2126-2133. LIPPINCOTT WILLIAMS & WILKINS

مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein E, NATIONAL INSTITUTE, Male, Pathology, MILD COGNITIVE IMPAIRMENT, SYMPTOMS, ATP-Binding Cassette Transporters/genetics, Disease, VARIANTS, DISEASE, 0302 clinical medicine, ASSOCIATION GUIDELINES, Medicine and Health Sciences, Family history, Age of Onset, Apolipoprotein E4/genetics, NEUROPATHOLOGIC, Medicine(all), DEMENTIA, Middle Aged, 3. Good health, ASSESSMENT, Disease Progression, Female, Alzheimer's disease, medicine.medical_specialty, Heterozygote, NEUROPATHOLOGIC ASSESSMENT, Alzheimer Disease/diagnostic imaging, Neuropathology, Biology, DIAGNOSIS, Article, 03 medical and health sciences, Alzheimer Disease, Internal medicine, medicine, Dementia, Humans, Genetic Predisposition to Disease, Biomarkers/cerebrospinal fluid, METAANALYSIS, Aged, Retrospective Studies, Biology and Life Sciences, Retrospective cohort study, medicine.disease, Brain/diagnostic imaging, 030104 developmental biology, Cerebrovascular Disorders/complications, ATP-Binding Cassette Transporters, Neurology (clinical), Human medicine, Age of onset, mutation, aged, 80 and over, 030217 neurology & neurosurgery, Genome-Wide Association Study