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1
المؤلفون: J. Gheuens, J. J. Martin, Michael Mullan, Gerd Multhaup, N.G. Irving, Antoon Vandenberghe, Hugh Gurling, W. Van Hul, A. Genthe, John Hardy, A. Wehnert, A. Barton, M. Salbaum, Bernhard Horsthemke, Marc Bruyland, H Backhovens, S. J. Richards, Konrad Beyreuther, C. Van Broeckhoven, A. Holland, Robert Williamson, Colin L. Masters, Peter Raeymaekers, Patrick Cras
المصدر: Nature
مصطلحات موضوعية: Adult, Male, Amyloid, Chromosomes, Human, Pair 21, Genetic Linkage, Locus (genetics), Disease, Biology, Alzheimer Disease, Genetic linkage, medicine, Humans, Senile plaques, Protein Precursors, Genetics, Amyloid beta-Peptides, Polymorphism, Genetic, Multidisciplinary, Molecular pathology, Chromosome Mapping, medicine.disease, Pedigree, Genes, Female, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73777dee0f802153a1b26c3c1a5967aTest
https://doi.org/10.1038/329153a0Test -
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المؤلفون: Victor Chan, Claude Stoll, Philippe Latour, François Ziegler, Elisabeth Ollagnon, Serge Perelman, Tanya Stojkovic, Christophe Vial, Antoon Vandenberghe, Pierre-Marie Gonnaud, Irène Maire
المصدر: Journal of the Peripheral Nervous System. 11:148-155
مصطلحات موضوعية: Adult, Male, Adolescent, DNA Mutational Analysis, Disease, Biology, medicine.disease_cause, Charcot-Marie-Tooth Disease, Sequence Analysis, Protein, Lysosome, medicine, Humans, Missense mutation, Coding region, Child, Gene, Late endosome, Aged, Genes, Dominant, Retrospective Studies, Family Health, Genetics, Mutation, General Neuroscience, Infant, Nuclear Proteins, Exons, Middle Aged, Pedigree, Phenotype, medicine.anatomical_structure, Child, Preschool, Mutation testing, Female, Neurology (clinical), Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d34af2f9a99e1e289ed83775a6598aTest
https://doi.org/10.1111/j.1085-9489.2006.00080.xTest -
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المؤلفون: Xavier Ferrer, Anne Vital, Yusuf A. Rajabally, Alain Lagueny, Jean Julien, Antoon Vandenberghe, Philippe Latour, Claude Vital
المصدر: Journal of the Peripheral Nervous System. 5:158-162
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, Biopsy, HIV Infections, Chronic inflammatory demyelinating polyneuropathy, Disease, Asymptomatic, Charcot-Marie-Tooth Disease, Gene duplication, Genetic predisposition, medicine, Humans, medicine.diagnostic_test, business.industry, General Neuroscience, Superficial peroneal nerve, Peroneal Nerve, medicine.disease, nervous system diseases, Chromosome 17 (human), Microscopy, Electron, Polyradiculoneuropathy, Chronic Inflammatory Demyelinating, Neurology (clinical), medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e693cb4c2e5671e8d421fdad1f3261Test
https://doi.org/10.1046/j.1529-8027.2000.00014.xTest -
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المؤلفون: Jean-Michel Vallat, Philippe Sindou, Antoon Vandenberghe, E. Lagrange, F. Tabaraud, Nicolas Lévy
المصدر: Muscle & Nerve. 22:1442-1447
مصطلحات موضوعية: education.field_of_study, Pathology, medicine.medical_specialty, Nerve biopsy, medicine.diagnostic_test, Physiology, business.industry, Motor nerve, Disease, medicine.disease, Central nervous system disease, Cellular and Molecular Neuroscience, Electrophysiology, Tooth disease, Degenerative disease, Physiology (medical), medicine, Connexin 32, Neurology (clinical), education, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6276f2b6da5ab0484b5e979e59a9aca3Test
https://doi.org/10.1002Test/(sici)1097-4598(199910)22:10<1442::aid-mus16>3.0.co;2-6 -
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المؤلفون: J.L Besse, Pierre-Marie Gonnaud, G. Chazot, Franck Sturtz, Antoon Vandenberghe
المصدر: Archives de Pédiatrie. 2:70-78
مصطلحات موضوعية: Pathology, medicine.medical_specialty, business.industry, Disease, medicine.disease, Muscle hypertrophy, Chromosome 17 (human), Central nervous system disease, Degenerative disease, Pediatrics, Perinatology and Child Health, medicine, Abnormality, business, Hereditary motor and sensory neuropathy, Pathological
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c2f16676a97e3bffbb9361ab0dc2999bTest
https://doi.org/10.1016/0929-693xTest(96)89813-7 -
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المؤلفون: Nicole Philip, Philippe Latour, Perrine Malzac, Amandine Boyer, P. Negre, Rafaëlle Bernard, Antoon Vandenberghe, Nicolas Lévy
المصدر: European journal of human genetics : EJHG. 10(5)
مصطلحات موضوعية: Genetic Markers, Male, Pediatrics, medicine.medical_specialty, Genetic counseling, Prenatal diagnosis, Disease, Genetic Heterogeneity, Charcot-Marie-Tooth Disease, Pregnancy, Prenatal Diagnosis, Gene duplication, Genetics, medicine, Humans, Genetics (clinical), Fetus, business.industry, Genetic heterogeneity, medicine.disease, Charcot-Marie-Tooth Disease Type 1A, Pedigree, Fetal Diseases, Female, business, Gene Deletion, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a586e28087ad8108865355fad3fe17fcTest
https://pubmed.ncbi.nlm.nih.gov/12082504Test -
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المؤلفون: Antoon Vandenberghe, Franck Sturtz, Guy Chazot
المصدر: Journal of the history of the neurosciences. 1(1)
مصطلحات موضوعية: medicine.medical_specialty, Neurology, medicine.diagnostic_test, business.industry, General Neuroscience, Genetic Diseases, Inborn, History, 19th Century, Disease, Current period, Electromyography, History, 20th Century, medicine.disease, United Kingdom, Tooth disease, History and Philosophy of Science, Charcot-Marie-Tooth Disease, medicine, Humans, Neurology (clinical), France, Hereditary motor and sensory neuropathy, business, Pathological, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02707d0e736c7ea4b34984281858080Test
https://pubmed.ncbi.nlm.nih.gov/11618415Test -
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المؤلفون: Ronald J. Polinsky, B. O'Donnell, Leonard L. Heston, A. Haynes, L. Bergamini, G. De Winter, H Backhovens, J. F. Foncin, L. Connor, C. Van Broeckhoven, Richard H. Myers, David A. Drachman, Stefano F. Cappa, K. Abe, Luigi Amaducci, John Hardy, J. J. Martin, Lindsay A. Farrer, Antoon Vandenberghe, H. Karlinsky, Richard Mayeux, L. Pinessi, C. Ruiz, M. E. Percy, Rossella Tupler, J. Henry, D. R. Crapper McLachlan, Robert G. Feldman, Martin N. Rossor, M.P. Montesi, Daniel A. Pollen, P. Frommelt, M. Mortilla, P Roques, James F. Gusella, M. Fracarro, Jonathan L. Haines, Voskresenskaya Ni, L James, Michael Mullan, Paul C. Watkins, V. A. Fried, Linda Nee, P. St. George-Hyslop, J. M. Cantu, Amalia C. Bruni, N. Nacmias, Sandro Sorbi, G. Vaula, Robert Williamson, Innocenzo Rainero, Alison Goate, Gavrilova Si, John H. Growdon, M. Vartanian, M. J. Owen, G. Gei, Marianne James, Stephen S. Rich, Rudolph E. Tanzi, J. Swearer, Marc Bruyland, Harry T. Orr, M. E. Franco, Silvia Piacentini, J. Gheuens
المصدر: Nature
مصطلحات موضوعية: Genetic Markers, Genetics, Heterozygote, Multidisciplinary, Chromosomes, Human, Pair 21, Genetic Linkage, Genetic heterogeneity, Pedigree chart, Disease, Biology, medicine.disease, Pedigree, Gene mapping, Alzheimer Disease, Genetic marker, Genetic linkage, medicine, Humans, Lod Score, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c81e757dca0d17ac30011aa71a54324Test
https://hdl.handle.net/10067/1434090151162165141Test -
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المؤلفون: Antoon Vandenberghe, A. Wehnert, J. J. Martin, W. Van Hul, G. Van Camp, C. Van Broeckhoven, H Backhovens, G. De Winter, J. Gheuens, Piet Stinissen, Marc Bruyland, P Raeymaekers
المصدر: Neuropsychopharmacology ISBN: 9783642740367
Neuropsychopharmacology / Bunney, W.E. [edit.]مصطلحات موضوعية: business.industry, Hippocampus, Pedigree chart, Autopsy, Disease, medicine.anatomical_structure, Cerebral cortex, Genetic marker, Immunology, Medicine, Human medicine, Senile plaques, Family history, business, Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2726cac7c4884c90f5c4cffe54fbee0fTest
https://doi.org/10.1007/978-3-642-74034-3_9Test -
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المؤلفون: Marc Bruyland, G. De Winter, Chantal Ceuterick, J. J. Martin, H. Van Heuverswijn, Konrad Beyreuther, Colin L. Masters, Patrick Cras, Antoon Vandenberghe, R. Dom, C. Van Broeckhoven, U. Lübke, J. Gheuens
المصدر: Neurology. 41:62-62
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Amyloid, Central nervous system, Disease, Degenerative disease, Belgium, Alzheimer Disease, medicine, Humans, Dementia, Early-onset Alzheimer's disease, Genes, Dominant, business.industry, Brain, medicine.disease, Immunohistochemistry, Pedigree, Microscopy, Electron, medicine.anatomical_structure, Neurofibrils, Female, Neurology (clinical), medicine.symptom, Alzheimer's disease, business, Myoclonus, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8444d32e61ef00fb6efc5fcafc9b6143Test
https://doi.org/10.1212/wnl.41.1.62Test