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1
المؤلفون: Philippe Latour, Jérôme De Seze, Patrick Vermersch, Antoon Vandenberghe, J.-F. Hurtevent, Tanya Stojkovic, Ghislaine Viet
المصدر: Neuromuscular Disorders. 14:261-264
مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, Pes cavus, Cord, DNA Mutational Analysis, Neural Conduction, Nerve Tissue Proteins, medicine.disease_cause, Frameshift mutation, Charcot-Marie-Tooth Disease, Reaction Time, Paralysis, Humans, Medicine, Vocal cord paralysis, Evoked Potentials, Genetics (clinical), Family Health, Mutation, business.industry, Genetic heterogeneity, Muscles, Siblings, Anatomy, medicine.disease, Respiratory Paralysis, Electric Stimulation, Stop codon, Neurology, Pediatrics, Perinatology and Child Health, Female, France, Neurology (clinical), medicine.symptom, business, Vocal Cord Paralysis, Thymidine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296f8faeeb710abed311eb508be974b7Test
https://doi.org/10.1016/j.nmd.2004.01.003Test -
2
المؤلفون: I Bernard, Alain Lagueny, A. Vital, Antoon Vandenberghe, G Le Masson, Yusuf A. Rajabally, Xavier Ferrer, Philippe Latour, Jean Julien, Claude Vital
المصدر: Neuromuscular Disorders. 9:361-367
مصطلحات موضوعية: Adult, Male, Restriction Mapping, Peripheral myelin, Biology, Gene mutation, medicine.disease_cause, Myelin, Nerve Fibers, Charcot-Marie-Tooth Disease, Peripheral nerve, Extracellular, medicine, Humans, Point Mutation, Peripheral Nerves, Muscle, Skeletal, Myelin Sheath, Polymorphism, Single-Stranded Conformational, Genetics (clinical), Genetics, Mutation, Chromosome Mapping, Exons, Middle Aged, Phenotype, Pedigree, Molecular analysis, medicine.anatomical_structure, Amino Acid Substitution, Neurology, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), Myelin P0 Protein, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39af762c45bb17f2a88c5a2a5e1e2afcTest
https://doi.org/10.1016/s0960-8966Test(99)00031-0 -
3
المؤلفون: Franck Sturtz, Guy Chazot, Antoon Vandenberghe, Cruz S, Mabin D, Philippe Latour, Mocquard Y, Fenoll B, LeFur Jm
المصدر: European Neurology. 38:26-30
مصطلحات موضوعية: Adult, Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Neural Conduction, Motor nerve, Biology, Nerve conduction velocity, Central nervous system disease, Degenerative disease, Charcot-Marie-Tooth Disease, Gene duplication, medicine, Humans, Age of Onset, Child, Genetics, Homozygote, Heterozygote advantage, DNA, Anatomy, medicine.disease, Phenotype, Pedigree, Electrophysiology, Chromosome 17 (human), Scoliosis, Neurology, Multigene Family, Female, Neurology (clinical), Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f900f9fac1443a26c257bec7be0d45bTest
https://doi.org/10.1159/000112898Test -
4
المؤلفون: C. Bonnebouche, B. Bady, Guy Chazot, F. Chauvin, M. Bost, Philippe Latour, Franck Sturtz, E. Ollagnon-Roman, Antoon Vandenberghe, Pierre-Marie Gonnaud
المصدر: European Neurology. 36:224-228
مصطلحات موضوعية: Pathology, medicine.medical_specialty, business.industry, Motor nerve conduction velocity, Motor nerve, Anatomy, medicine.disease, Median nerve, Central nervous system disease, Chromosome 17 (human), Degenerative disease, Neurology, Peripheral nerve, Gene duplication, medicine, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0b4e889ac538f3b0fa8795145d82d18fTest
https://doi.org/10.1159/000117254Test -
5
المؤلفون: Philippe Sindou, A. J. Steck, Jean-Michel Vallat, F. Tabaraud, Pierre-Marie Preux, Antoon Vandenberghe
المساهمون: Service de Neurologie [CHU Limoges], CHU Limoges, Department of Neurology, University Hospital, 2 Avenue Martin Luther King, 87042 Limoges, Franc, Neuroépidémiologie Tropicale (NET), Institut Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST), Université de Limoges (UNILIM)-Université de Limoges (UNILIM)-CHU Limoges-Institut d'Epidémiologie Neurologique et de Neurologie Tropicale-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Molecular Neurogenetics, Claude Bernard University, Lyon I, France, Department of Neurology, UniversityClinics, Basel, Switzerland.
المصدر: Annals of Neurology
Annals of Neurology, Wiley, 2000, 47 (6), pp.808-811. ⟨10.1002/1531-8249(200006)47:63.0.CO;2-8⟩مصطلحات موضوعية: chemistry.chemical_classification, Pathology, medicine.medical_specialty, business.industry, Immunoelectron microscopy, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, medicine.disease, 3. Good health, law.invention, Myelin, medicine.anatomical_structure, Neurology, chemistry, law, Immunopathology, Monoclonal, Medicine, Neurology (clinical), Electron microscope, business, Dysglobulinemia, Glycoprotein, Polyneuropathy, ComputingMilieux_MISCELLANEOUS
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a7470259c8c55079659e7458d772b4Test
https://hal.archives-ouvertes.fr/hal-02504280Test -
6
المؤلفون: Jean-Christophe Antoine, Emmanuel Corbillon, Franck Sturtz, Françoise Chapon, Philippe Latour, Patrick Calvas, Anne Fabreguette, Antoon Vandenberghe, Guy Chazot, Danielle Pham-Dinh, André Dautigny, Catherine Ressot, Michel Boucherat, Françoise Blanquet-Grossard, Elisabeth Ollagnon
المصدر: European neurology. 37(1)
مصطلحات موضوعية: Male, X Chromosome, DNA Mutational Analysis, X-linked form, Biology, Polymerase Chain Reaction, Connexins, Degenerative disease, Charcot-Marie-Tooth Disease, medicine, Missense mutation, Humans, education, Gene, X chromosome, Polymorphism, Single-Stranded Conformational, Sex Chromosome Aberrations, Genetics, education.field_of_study, Chromosome, medicine.disease, Pedigree, Transmembrane domain, Neurology, Connexin 32, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac10de2b841de7b482e739be77109be0Test
https://pubmed.ncbi.nlm.nih.gov/9018031Test -
7
المؤلفون: C. Vial, Antoon Vandenberghe, J. M. Warter, C. Bonnebouche, Pierre-Marie Gonnaud, B. Bady, A. S. Brechard, V. Fourbil, C. Tranchant, Guy Chazot, Franck Sturtz
المصدر: Acta neurologica Scandinavica. 92(4)
مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, Adolescent, Genotype, Asymptomatic, Paralysis, medicine, Humans, Point Mutation, Allele, Genotyping, Alleles, Ulnar Nerve, Palsy, business.industry, Point mutation, Peroneal Nerve, General Medicine, DNA, Middle Aged, medicine.disease, Dermatology, Median Nerve, Neurology, Mutagenesis, Female, Neurology (clinical), medicine.symptom, Chromosome Deletion, Tibial Nerve, business, Hereditary Sensory and Motor Neuropathy, Polyneuropathy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba75f66a17e7081c34a569f73ae7c6cbTest
https://pubmed.ncbi.nlm.nih.gov/8848937Test -
8
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: Antoon Vandenberghe, Philippe Latour, A Brice, E. Le Guern, N. Ravisé, Judith Lopes, Victor Ionasescu, S. Tardieu
المصدر: Neuromuscular Disorders. 7:471
مصطلحات موضوعية: Genetics, Neurology, Pediatrics, Perinatology and Child Health, Crossover, Breakpoint, Neurology (clinical), Biology, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9dc7ce1f50a2a463586983652c553805Test
https://doi.org/10.1016/s0960-8966Test(97)87340-3 -
10
المؤلفون: M. Barat, Claude Vital, Alain Lagueny, A. Vital, Yusuf A. Rajabally, Antoon Vandenberghe, D. Fontan, P. Henry, Jean Julien, Philippe Latour, A. Arnaud
المصدر: Neuromuscular Disorders. 7:473
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Neurology, Chemistry, Pediatrics, Perinatology and Child Health, medicine, Neurology (clinical), Genetics (clinical), Onion bulb formation, Surgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c0d8ce5dcc5da08441ac3400ed83984aTest
https://doi.org/10.1016/s0960-8966Test(97)87348-8