학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 4건 | 목록 1~10
Academic Journal
Benkirane M; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; PhyMedExp Univ Montpellier, CNRS UMR 9214, INSERM U1046, 34090 Montpellier, France.; Department of Medical Genetics, Laboratory of Genomics Medicine, Sorbonne University, APHP, 75006 Paris, France.; Bonhomme M; CRBM (Centre de Recherche en Biologie cellulaire de Montpellier), CNRS, Université de Montpellier, 34293 Montpellier, France.; Morsy H; Department of Neuromuscular Diseases, UCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.; Human Genetics Department, Medical Research Institute, Alexandria University, Alexandria 21561, Egypt.; Safgren SL; Department of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.; Marelli C; MMDN, Univ Montpellier, EPHE, INSERM, Montpellier, France; Expert center for Neurogenetic Diseases, CHU of Montpellier, 34095 Montpellier, France.; Chaussenot A; Department of Medical Genetics, CHU of Nice, 06000 Nice, France.; Smedley D; William Harvey Research Institute, Clinical Pharmacology and Precision Medicine, Queen Mary University of London, London EC1M 6BQ, UK.; Cipriani V; William Harvey Research Institute, Clinical Pharmacology and Precision Medicine, Queen Mary University of London, London EC1M 6BQ, UK.; UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.; UCL Genetics Institute, University College London, London WC1E 6BT, UK.; de Sainte-Agathe JM; Department of Medical Genetics, Laboratory of Genomics Medicine, Sorbonne University, APHP, 75006 Paris, France.; Ding C; Institute of human genetics, University of Medicine Mainz, Mainz 55128, Germany.; Larrieu L; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; Vestito L; William Harvey Research Institute, Clinical Pharmacology and Precision Medicine, Queen Mary University of London, London EC1M 6BQ, UK.; Margot H; Department of Medical Genetics, CHU of Bordeaux, 33404 Bordeaux, France.; Lesca G; Department of Medical Genetics, University Hospitals of Lyon, and Université Claude Bernard Lyon1, 69500 Lyon, France.; Ramond F; Department of Medical Genetics, CHU of Saint-Etienne, 42055 Saint-Etienne, France.; Castrioto A; Univ. Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Neurology Department, 38706 Grenoble, France.; Baux D; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; INM, Institut des Neurosciences Montpellier, INSERM, 34000 Montpellier, France.; Montpellier BioInformatics for Clinical Diagnosis (MOBIDIC), Molecular Medicine and Genomics Platform (PMMG), CHU Montpellier, 34295 Montpellier, France.; Verheijen J; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.; Sansa E; Department of Neurogenetics, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, Institute of Neurology, London WC1N 3BG, UK.; Giunti P; Department of Neurogenetics, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, Institute of Neurology, London WC1N 3BG, UK.; Haetty A; INM, Institut des Neurosciences Montpellier, INSERM, 34000 Montpellier, France.; Bergougnoux A; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; PhyMedExp Univ Montpellier, CNRS UMR 9214, INSERM U1046, 34090 Montpellier, France.; Pointaux M; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; Ardouin O; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; Montpellier BioInformatics for Clinical Diagnosis (MOBIDIC), Molecular Medicine and Genomics Platform (PMMG), CHU Montpellier, 34295 Montpellier, France.; Van Goethem C; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; Montpellier BioInformatics for Clinical Diagnosis (MOBIDIC), Molecular Medicine and Genomics Platform (PMMG), CHU Montpellier, 34295 Montpellier, France.; Vincent MC; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; Hadjivassiliou M; Academic Department of Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield S10 2HQ, UK.; Cossée M; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; PhyMedExp Univ Montpellier, CNRS UMR 9214, INSERM U1046, 34090 Montpellier, France.; Rouaud T; Department of Neurology, CHU of Nantes, 44000 Nantes, France.; Bartsch O; Institute of human genetics, University of Medicine Mainz, Mainz 55128, Germany.; Freeman WD; Department of Neurology, Mayo Clinic Jacksonville, FL 32224, USA.; Wierenga KJ; Department of Clinical Genomics, Mayo Clinic, Jacksonville, FL 32224, USA.; Klee EW; Department of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55905, USA.; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.; Vandrovcova J; Department of Neuromuscular Diseases, UCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.; Houlden H; Department of Neuromuscular Diseases, UCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.; Debant A; CRBM (Centre de Recherche en Biologie cellulaire de Montpellier), CNRS, Université de Montpellier, 34293 Montpellier, France.; Koenig M; Laboratoire de Génétique moléculaire, Institut Universitaire de Recherche Clinique, CHU of Montpellier, 34090 Montpellier, France.; PhyMedExp Univ Montpellier, CNRS UMR 9214, INSERM U1046, 34090 Montpellier, France.
Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE
Academic Journal
Benkirane M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Da Cunha D; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Marelli C; Department of Neurology, Montpellier Hospital, Montpellier, France.; Molecular Mechanisms of Neurodegenerative Dementia (MMDN), EPHE University of Montpellier, INSERM, Montpellier, France.; Larrieu L; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Renaud M; Department of Medical Genetics, Nancy Hospital, Nancy, France.; Varilh J; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Pointaux M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Baux D; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Ardouin O; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Vangoethem C; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Taulan M; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Daumas Duport B; Department of Radiology, Nantes Hospital, Nantes, France.; Bergougnoux A; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Corbillé AG; Department of Neurology, Nantes Hospital, Nantes, France.; Cossée M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Juntas Morales R; Department of Neurology, Montpellier Hospital, Montpellier, France.; Tuffery-Giraud S; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Koenig M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.; Isidor B; Department of Medical Genetics, Nantes Hospital, Nantes, France.; Vincent MC; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE
Academic Journal
Benkirane M; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Marelli C; Expert Centre for Neurogenetic Diseases and Adult Mitochondrial and Metabolic Diseases, Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier; Molecular Mechanisms of Neurodegenerative Dementia (MMDN), EPHE, INSERM, Université de Montpellier, Montpellier, France.; Guissart C; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Roubertie A; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; INSERM, Institut des Neurosciences de Montpellier, Montpellier, France.; Ollagnon E; Department of Medical Genetics and Reference Centre for Neurological and Neuromuscular Diseases, Croix-Rousse Hospital, Lyon, France.; Choumert A; Department of Rare Neurological Diseases, CHU de la Réunion, Saint-Pierre, France.; Fluchère F; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Magne FO; Department of Neurology, Purpan Hospital, CHU de Toulouse, Toulouse, France.; Halleb Y; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Renaud M; Departments of Genetics and of Neurology, CHU de Nancy, Nancy, France.; Larrieu L; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Baux D; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Patat O; Department of Clinical Genetics, Purpan Hospital, CHU de Toulouse, Toulouse, France.; Bousquet I; Department of Medical Genetics and Reference Centre for Neurological and Neuromuscular Diseases, Croix-Rousse Hospital, Lyon, France.; Ravel JM; Departments of Genetics and of Neurology, CHU de Nancy, Nancy, France.; Cuntz-Shadfar D; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Sarret C; Department of Medical Genetics, Estaing Hospital, CHU de Clermont-Ferrand, Clermont-Ferrand, France.; Ayrignac X; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Rolland A; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Morales R; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Pointaux M; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Lieutard-Haag C; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France.; Laurens B; Departement of Neurology, Groupe Hospitalier Pellegrin, CHU de Bordeaux, Institute for Neurodegenerative Diseases, CNRS-UMR, Université de Bordeaux, Bordeaux, France.; Tillikete C; Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Bron, France.; Bernard E; Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Bron, France.; Institut NeuroMyoGène, INSERM-CNRS-UMR, Université Claude Bernard, Lyon, France.; Mallaret M; Department of Functional Explorations of the Nervous System, CHU de Grenoble, Grenoble, France.; Carra-Dallière C; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Tranchant C; Department of Neurology, Hautepierre Hospital, CHU de Strasbourg, Strasbourg, France.; Meyer P; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; PhyMedExp, INSERM, University of Montpellier, CNRS, Montpellier, France.; Damaj L; Department of Clinical Genetics, Centre de Référence Maladies Rares Anomalies du Développement, CHU de Rennes, Rennes, France.; Pasquier L; Department of Clinical Genetics, Centre de Référence Maladies Rares Anomalies du Développement, CHU de Rennes, Rennes, France.; Acquaviva C; Department of Hereditary Metabolic Diseases, Centre de Biologie et Pathologie Est, CHU de Lyon et UMR, Bron, France.; Chaussenot A; Department of Medical Genetics, National Centre for Mitochondrial Diseases, CHU de Nice, Nice, France.; Isidor B; Department of Medical Genetics, CHU de Nantes, Nantes, France.; Nguyen K; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Camu W; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Eusebio A; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Carrière N; Department of Neurology, Roger Salengro Hospital, CHU de Lille, Lille, France.; Riquet A; Department of Pediatrics Neurology, Roger Salengro Hospital, CHU de Lille, Lille, France.; Thouvenot E; Department of Neurology, CHU de Nîmes, Nîmes, France.; Gonzales V; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Carme E; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Attarian S; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Odent S; Department of Clinical Genetics, Centre de Référence Maladies Rares Anomalies du Développement, CHU de Rennes, Rennes, France.; Castrioto A; Department of Functional Explorations of the Nervous System, CHU de Grenoble, Grenoble, France.; Ewenczyk C; Neurogenetics Reference Centre, Hôpital de la Pitié-Salpêtrière, Assistance Publique- Hôpitaux de Paris (AP-HP), Paris, France.; Charles P; Neurogenetics Reference Centre, Hôpital de la Pitié-Salpêtrière, Assistance Publique- Hôpitaux de Paris (AP-HP), Paris, France.; Kremer L; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Sissaoui S; Department of Pediatrics, Hôpital Necker-Enfant Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Bahi-Buisson N; Department of Pediatrics, Hôpital Necker-Enfant Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Kaphan E; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Degardin A; Department of Neurology, Roger Salengro Hospital, CHU de Lille, Lille, France.; Doray B; Department of Medical Genetics, CHU de la Réunion, Saint-Denis, France.; Julia S; Department of Clinical Genetics, Purpan Hospital, CHU de Toulouse, Toulouse, France.; Remerand G; Department of Neonatology, Estaing Hospital, CHU de Clermont-Ferrand, Clermont-Ferrand, France.; Fraix V; Department of Functional Explorations of the Nervous System, CHU de Grenoble, Grenoble, France.; Haidar LA; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Lazaro L; Department of Pediatrics, CH de la Côte Basque-Bayonne, Bayonne, France.; Laugel V; Department of Pediatrics, Hautepierre Hospital, CHU de Strasbourg, Strasbourg, France.; Villega F; Department of Pediatrics, Groupe Hospitalier Pellegrin, CHU de Bordeaux; Institute for Interdisciplinary Neurosciences (IINS), CNRS -UMR, Université de Bordeaux, Bordeaux, France.; Charlin C; Department of Rare Neurological Diseases, CHU de la Réunion, Saint-Pierre, France.; Frismand S; Departments of Genetics and of Neurology, CHU de Nancy, Nancy, France.; Moreira MC; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Witjas T; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Francannet C; Department of Medical Genetics, Estaing Hospital, CHU de Clermont-Ferrand, Clermont-Ferrand, France.; Walther-Louvier U; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Fradin M; Department of Clinical Genetics, Centre de Référence Maladies Rares Anomalies du Développement, CHU de Rennes, Rennes, France.; Chabrol B; Departement of Pediatrics, La Timone Hospital, CHU de Marseille, Marseille, France.; Fluss J; Pediatric Neurology Unit, Geneva Children's Hospital, Genève, Switzerland.; Bieth E; Department of Clinical Genetics, Purpan Hospital, CHU de Toulouse, Toulouse, France.; Castelnovo G; Department of Neurology, CHU de Nîmes, Nîmes, France.; Vergnet S; Departement of Neurology, Groupe Hospitalier Pellegrin, CHU de Bordeaux, Institute for Neurodegenerative Diseases, CNRS-UMR, Université de Bordeaux, Bordeaux, France.; Meunier I; INSERM, Institut des Neurosciences de Montpellier, Montpellier, France.; Genetics of Sensory Diseases, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Verloes A; Federation of Genetics, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Brischoux-Boucher E; Department of Medical Genetics, Hôpital Saint-Jacques, CHU de Besançon, Centre de Génétique Humaine, Université de Franche-Comté, Besançon, France.; Coubes C; Department of Medical Genetics, Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Geneviève D; Department of Medical Genetics, Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Lebouc N; Department of Neuroradiology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Azulay JP; Department of Neurology, La Timone Hospital, CHU de Marseille, Marseille, France.; Anheim M; Department of Neurology, Hautepierre Hospital, CHU de Strasbourg, Strasbourg, France.; Goizet C; Department of Medical Genetics, Pellegrin Hospital, CHU de Bordeaux, Bordeaux, France.; Rivier F; Department of Pediatrics, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; PhyMedExp, INSERM, University of Montpellier, CNRS, Montpellier, France.; Labauge P; Department of Neurology, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France.; Calvas P; Department of Clinical Genetics, Purpan Hospital, CHU de Toulouse, Toulouse, France.; Koenig M; PhyMedExp, Institut Universitaire de Recherche Clinique, UMR_CNRS-Université de Montpellier, INSERM, CHU de Montpellier, Montpellier, France. michel.koenig@inserm.fr.
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
Academic Journal
Ravel JM; Service de Génétique Médicale, Hôpitaux de Brabois, CHRU de Nancy, Rue du Morvan, 54500, Vandoeuvre-lès-Nancy, France.; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Benkirane M; Laboratoire de Génétique Moléculaire, CHU Montpellier, EA7402, Montpellier, France.; EA7402 Institut Universitaire de Recherche Clinique, Université de Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier cedex 5, France.; Calmels N; Laboratoires de Diagnostic Génétique, Institut de Génétique Médicale D'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Marelli C; Expert Centre for Neurogenetic Diseases and Adult Mitochondrial and Metabolic Diseases, University Montpellier, CHU, Montpellier, France.; MMDN, University Montpellier, EPHE, INSERM, Montpellier, France.; Ory-Magne F; Service de Neurologie, CHU Purpan, Inserm U825, Toulouse, France.; Ewenczyk C; Sorbonne Université, Institut du Cerveau et de la Moelle Épinière (ICM), AP-HP, INSERM, CNRS, University Hospital Pitié-Salpêtrière, Paris, France.; Service de génétique clinique, Hôpital Pitié-Salpêtrière, APHP, Paris, France.; Halleb Y; Laboratoire de Génétique Moléculaire, CHU Montpellier, EA7402, Montpellier, France.; EA7402 Institut Universitaire de Recherche Clinique, Université de Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier cedex 5, France.; Tison F; Institut des Maladies Neurodégénératives, Univ. Bordeaux, CNRS, Bordeaux, France.; Centre Mémoire de Ressources et de Recherches, CHU de Bordeaux, Pôle de Neurosciences Cliniques, Bordeaux, France.; Lecocq C; Service de Neurologie, Centre Hospitalier de Haguenau, Haguenau, France.; Pische G; Service de Neurologie, Centre Hospitalier de Haguenau, Haguenau, France.; Casenave P; Service de Neurologie, Hôpital Robert Boulin, Libourne, France.; Chaussenot A; Service de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital de l'Archet 2, Nice, France.; Frismand S; Service de Neurologie, CHRU Nancy, Nancy, France.; Tyvaert L; Service de Neurologie, CHRU Nancy, Nancy, France.; Larrieu L; Laboratoire de Génétique Moléculaire, CHU Montpellier, EA7402, Montpellier, France.; EA7402 Institut Universitaire de Recherche Clinique, Université de Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier cedex 5, France.; Pointaux M; Laboratoire de Génétique Moléculaire, CHU Montpellier, EA7402, Montpellier, France.; EA7402 Institut Universitaire de Recherche Clinique, Université de Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier cedex 5, France.; Drouot N; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France.; Bossenmeyer-Pourié C; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Oussalah A; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital of Nancy, 54000, Nancy, France.; Guéant JL; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital of Nancy, 54000, Nancy, France.; Leheup B; Service de Génétique Médicale, Hôpitaux de Brabois, CHRU de Nancy, Rue du Morvan, 54500, Vandoeuvre-lès-Nancy, France.; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Bonnet C; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Laboratoire de génétique médicale, CHRU Nancy, Nancy, France.; Anheim M; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France.; Service de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1 avenue Molière, 67098, Cedex, Strasbourg, France.; Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.; Tranchant C; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France.; Service de Neurologie, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, 1 avenue Molière, 67098, Cedex, Strasbourg, France.; Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.; Lambert L; Service de Génétique Médicale, Hôpitaux de Brabois, CHRU de Nancy, Rue du Morvan, 54500, Vandoeuvre-lès-Nancy, France.; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France.; Chelly J; Laboratoires de Diagnostic Génétique, Institut de Génétique Médicale D'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France.; Koenig M; Laboratoire de Génétique Moléculaire, CHU Montpellier, EA7402, Montpellier, France. michel.koenig@inserm.fr.; EA7402 Institut Universitaire de Recherche Clinique, Université de Montpellier, 641 Avenue du Doyen Gaston Giraud, 34093, Montpellier cedex 5, France. michel.koenig@inserm.fr.; Renaud M; Service de Génétique Médicale, Hôpitaux de Brabois, CHRU de Nancy, Rue du Morvan, 54500, Vandoeuvre-lès-Nancy, France. m.renaud2@chru-nancy.fr.; University of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, 54000, Nancy, France. m.renaud2@chru-nancy.fr.; Service de Neurologie, CHRU Nancy, Nancy, France. m.renaud2@chru-nancy.fr.
Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1459 (Electronic) Linking ISSN: 03405354 NLM ISO Abbreviation: J Neurol Subsets: MEDLINE
검색 결과 제한하기
제한된 항목
[검색어] Pointaux, M.
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어