المؤلفون: Ahmad, Shahzad, Milan, Marta Del Campo, Hankemeier, Thomas, Stomrud, Erik, Mattsson-Carlgren, Niklas, Scheltens, Philip, van der Flier, Wiesje M, Ikram, M Arfan, Malarstig, Anders, Teunissen, Charlotte E, Amin, Najaf, van Duijn, Cornelia M, Hansson, Oskar, Demirkan, Ayse, Agustin, Ruiz, Sáez, Maria E, Giagtzoglou, Nikolaos, Cabrera-Socorro, Alfredo, Bakker, Margot H M, Ramirez, Alfredo

المصدر: Scientific reports 10(1), 8233 (2020). doi:10.1038/s41598-020-65038-5

مصطلحات موضوعية: info:eu-repo/classification/ddc/600, Alzheimer Disease: metabolism, Apolipoprotein E4: genetics, Apolipoprotein E4: metabolism, Biomarkers: blood, Cadherins: metabolism, Genetic Carrier Screening, Humans, Thiolester Hydrolases: metabolism

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:32427856; info:eu-repo/semantics/altIdentifier/issn/2045-2322; https://pub.dzneTest.de/record/153314; https://pub.dzneTest.de/search?p=id:%22DZNE-2020-01311%22

الإتاحة: https://doi.org/10.1038/s41598-020-65038-5Test
https://pub.dzneTest.de/record/153314
https://pub.dzneTest.de/search?p=id:%22DZNE-2020-01311%22

المؤلفون: Brockmann, K., Lohmann, K.

المصدر: Der Nervenarzt 88(7), 713-719 (2017). doi:10.1007/s00115-017-0348-5

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, DNA Mutational Analysis, Dystonia: diagnosis, Dystonia: genetics, Essential Tremor: diagnosis, Essential Tremor: genetics, Genetic Association Studies, Genetic Carrier Screening, Genetic Diseases, Inborn: diagnosis, Inborn: genetics, Genetic Variation: genetics, Genome-Wide Association Study, Glucosylceramidase: genetics, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2: genetics, Movement Disorders: diagnosis, Movement Disorders: genetics, Parkinson Disease: diagnosis, Parkinson Disease: genetics, Restless Legs Syndrome: diagnosis, Restless Legs Syndrome: genetics, Risk Factors, LRRK2 protein, human, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Glucosylceramidase

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0028-2804; info:eu-repo/semantics/altIdentifier/issn/1433-0407; info:eu-repo/semantics/altIdentifier/pmid/pmid:28536875; https://pub.dzneTest.de/record/139360; https://pub.dzneTest.de/search?p=id:%22DZNE-2020-05682%22

الإتاحة: https://doi.org/10.1007/s00115-017-0348-5Test
https://pub.dzneTest.de/record/139360
https://pub.dzneTest.de/search?p=id:%22DZNE-2020-05682%22

المؤلفون: Schuberth, M., Levin, J., Diehl-Schmid, J., Biskup, S., Danek, A., Sawalhe, D., Schwarzkopf, R., von Baumgarten, L., Ertl-Wagner, B., Rominger, A., Arzberger, T., Kretzschmar, H. A., Froböse, T.

المصدر: Der Nervenarzt 85(4), 465-470 (2014). doi:10.1007/s00115-014-4052-4

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adult, Axons: pathology, Biopsy, Brain: pathology, Female, Fluorodeoxyglucose F18, Follow-Up Studies, Frontal Lobe: pathology, Genetic Carrier Screening, Genetic Testing, Humans, Leukoencephalopathies: diagnosis, Leukoencephalopathies: genetics, Magnetic Resonance Imaging, Male, Microglia, Middle Aged, Multimodal Imaging, Mutation, Missense: genetics, Nerve Fibers, Myelinated: pathology, Neuropsychological Tests: statistics & numerical data, Phenotype, Positron-Emission Tomography, Psychometrics, Receptor, Macrophage Colony-Stimulating Factor: genetics, Spheroids

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1433-0407; info:eu-repo/semantics/altIdentifier/pmid/pmid:24706185; info:eu-repo/semantics/altIdentifier/issn/0028-2804; https://pub.dzneTest.de/record/137351; https://pub.dzneTest.de/search?p=id:%22DZNE-2020-03673%22

الإتاحة: https://doi.org/10.1007/s00115-014-4052-4Test
https://pub.dzneTest.de/record/137351
https://pub.dzneTest.de/search?p=id:%22DZNE-2020-03673%22

المؤلفون: Ehninger, Dan, Silva, Alcino J

المصدر: Behavior genetics 41(3), 357-363 (2010). doi:10.1007/s10519-010-9398-1

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Animals, Anxiety: genetics, Disease Models, Animal, Female, Genes, Dominant: genetics, Genetic Carrier Screening, Hippocampus: physiopathology, Humans, Learning Disabilities: genetics, Learning Disabilities: physiopathology, Male, Memory Disorders: genetics, Memory Disorders: physiopathology, Mice, Inbred C57BL, Transgenic, Phenotype, Tuberous Sclerosis: genetics, Tuberous Sclerosis: physiopathology, Tuberous Sclerosis Complex 2 Protein, Tumor Suppressor Proteins: genetics, TSC2 protein, human, mouse, Tumor Suppressor Proteins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0005-7851; info:eu-repo/semantics/altIdentifier/issn/1573-3297; info:eu-repo/semantics/altIdentifier/pmid/pmid:20882401; info:eu-repo/semantics/altIdentifier/issn/0001-8244; https://pub.dzneTest.de/record/136241; https://pub.dzneTest.de/search?p=id:%22DZNE-2020-02563%22

الإتاحة: https://doi.org/10.1007/s10519-010-9398-1Test
https://pub.dzneTest.de/record/136241
https://pub.dzneTest.de/search?p=id:%22DZNE-2020-02563%22

المؤلفون: Roder, Constantin, Peters, Vera, Kasuya, Hidetoshi, Nishizawa, Tsutomu, Wakita, Sho, Berg, Daniela, Schulte, Claudia, Khan, Nadia, Tatagiba, Marcos, Krischek, Boris

المصدر: European journal of paediatric neurology 15(2), 117-122 (2011). doi:10.1016/j.ejpn.2010.09.002

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Actins: analysis, Actins: genetics, Adolescent, Adult, Aged, Child, Preschool, Cohort Studies, Europe: epidemiology, Europe: ethnology, Genetic Carrier Screening, Genetic Predisposition to Disease: epidemiology, Genetic Predisposition to Disease: genetics, Humans, Middle Aged, Moyamoya Disease: ethnology, Moyamoya Disease: genetics, Moyamoya Disease: metabolism, Mutation: genetics, Young Adult, ACTA2 protein, human, Actins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1090-3798; info:eu-repo/semantics/altIdentifier/pmid/pmid:20970362; info:eu-repo/semantics/altIdentifier/issn/1532-2130; https://pub.dzneTest.de/record/136208; https://pub.dzneTest.de/search?p=id:%22DZNE-2020-02530%22

الإتاحة: https://doi.org/10.1016/j.ejpn.2010.09.002Test
https://pub.dzneTest.de/record/136208
https://pub.dzneTest.de/search?p=id:%22DZNE-2020-02530%22