학술논문
'학술논문'
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1~10
Academic Journal
H. Mosbah; B. Donadille; C. Vatier; S. Janmaat; M. Atlan; C. Badens; P. Barat; S. Béliard; J. Beltrand; R. Ben Yaou; E. Bismuth; F. Boccara; B. Cariou; M. Chaouat; G. Charriot; S. Christin-Maitre; M. De Kerdanet; B. Delemer; E. Disse; N. Dubois; B. Eymard; B. Fève; O. Lascols; P. Mathurin; E. Nobécourt; A. Poujol-Robert; G. Prevost; P. Richard; J. Sellam; I. Tauveron; D. Treboz; B. Vergès; V. Vermot-Desroches; K. Wahbi; I. Jéru; M. C. Vantyghem; C. Vigouroux
Orphanet Journal of Rare Diseases, Vol 17, Iss S1, Pp 1-23 (2022)
Academic Journal
Adam Jackson; Sheng-Jia Lin; Elizabeth A. Jones; Kate E. Chandler; David Orr; Celia Moss; Zahra Haider; Gavin Ryan; Simon Holden; Mike Harrison; Nigel Burrows; Wendy D. Jones; Mary Loveless; Cassidy Petree; Helen Stewart; Karen Low; Deirdre Donnelly; Simon Lovell; Konstantina Drosou; Gaurav K. Varshney; Siddharth Banka; J.C. Ambrose; P. Arumugam; R. Bevers; M. Bleda; F. Boardman-Pretty; C.R. Boustred; H. Brittain; M.A. Brown; M.J. Caulfield; G.C. Chan; A. Giess; J.N. Griffin; A. Hamblin; S. Henderson; T.J.P. Hubbard; R. Jackson; L.J. Jones; D. Kasperaviciute; M. Kayikci; A. Kousathanas; L. Lahnstein; A. Lakey; S.E.A. Leigh; I.U.S. Leong; F.J. Lopez; F. Maleady-Crowe; M. McEntagart; F. Minneci; J. Mitchell; L. Moutsianas; M. Mueller; N. Murugaesu; A.C. Need; P. O‘Donovan; C.A. Odhams; C. Patch; D. Perez-Gil; M.B. Pereira; J. Pullinger; T. Rahim; A. Rendon; T. Rogers; K. Savage; K. Sawant; R.H. Scott; A. Siddiq; A. Sieghart; S.C. Smith; A. Sosinsky; A. Stuckey; M. Tanguy; A.L. Taylor Tavares; E.R.A. Thomas; S.R. Thompson; A. Tucci; M.J. Welland; E. Williams; K. Witkowska; S.M. Wood; M. Zarowiecki; Olaf Riess; Tobias B. Haack; Holm Graessner; Birte Zurek; Kornelia Ellwanger; Stephan Ossowski; German Demidov; Marc Sturm; Julia M. Schulze-Hentrich; Rebecca Schüle; Christoph Kessler; Melanie Wayand; Matthis Synofzik; Carlo Wilke; Andreas Traschütz; Ludger Schöls; Holger Hengel; Peter Heutink; Han Brunner; Hans Scheffer; Nicoline Hoogerbrugge; Alexander Hoischen; Peter A.C. ’t Hoen; Lisenka E.L.M. Vissers; Christian Gilissen; Wouter Steyaert; Karolis Sablauskas; Richarda M. de Voer; Erik-Jan Kamsteeg; Bart van de Warrenburg; Nienke van Os; Iris te Paske; Erik Janssen; Elke de Boer; Marloes Steehouwer; Burcu Yaldiz; Tjitske Kleefstra; Anthony J. Brookes; Colin Veal; Spencer Gibson; Marc Wadsley; Mehdi Mehtarizadeh; Umar Riaz; Greg Warren; Farid Yavari Dizjikan; Thomas Shorter; Ana Töpf; Volker Straub; Chiara Marini Bettolo; Sabine Specht; Jill Clayton-Smith; Elizabeth Alexander; Laurence Faivre; Christel Thauvin; Antonio Vitobello; Anne-Sophie Denommé-Pichon; Yannis Duffourd; Emilie Tisserant; Ange-Line Bruel; Christine Peyron; Aurore Pélissier; Sergi Beltran; Ivo Glynne Gut; Steven Laurie; Davide Piscia; Leslie Matalonga; Anastasios Papakonstantinou; Gemma Bullich; Alberto Corvo; Carles Garcia; Marcos Fernandez-Callejo; Carles Hernández; Daniel Picó; Ida Paramonov; Hanns Lochmüller; Gulcin Gumus; Virginie Bros-Facer; Ana Rath; Marc Hanauer; Annie Olry; David Lagorce; Svitlana Havrylenko; Katia Izem; Fanny Rigour; Giovanni Stevanin; Alexandra Durr; Claire-Sophie Davoine; Léna Guillot-Noel; Anna Heinzmann; Giulia Coarelli; Gisèle Bonne; Teresinha Evangelista; Valérie Allamand; Isabelle Nelson; Rabah Ben Yaou; Corinne Metay; Bruno Eymard; Enzo Cohen; Antonio Atalaia; Tanya Stojkovic; Milan Macek, Jr.; Marek Turnovec; Dana Thomasová; Radka Pourová Kremliková; Vera Franková; Markéta Havlovicová; Vlastimil Kremlik; Helen Parkinson; Thomas Keane; Dylan Spalding; Alexander Senf; Peter Robinson; Daniel Danis; Glenn Robert; Alessia Costa; Christine Patch; Mike Hanna; Henry Houlden; Mary Reilly; Jana Vandrovcova; Francesco Muntoni; Irina Zaharieva; Anna Sarkozy; Vincent Timmerman; Jonathan Baets; Liedewei Van de Vondel; Danique Beijer; Peter de Jonghe; Vincenzo Nigro; Sandro Banfi; Annalaura Torella; Francesco Musacchia; Giulio Piluso; Alessandra Ferlini; Rita Selvatici; Rachele Rossi; Marcella Neri; Stefan Aretz; Isabel Spier; Anna Katharina Sommer; Sophia Peters; Carla Oliveira; Jose Garcia Pelaez; Ana Rita Matos; Celina São José; Marta Ferreira; Irene Gullo; Susana Fernandes; Luzia Garrido; Pedro Ferreira; Fátima Carneiro; Morris A. Swertz; Lennart Johansson; Joeri K. van der Velde; Gerben van der Vries; Pieter B. Neerincx; Dieuwke Roelofs-Prins; Sebastian Köhler; Alison Metcalfe; Alain Verloes; Séverine Drunat; Caroline Rooryck; Aurelien Trimouille; Raffaele Castello; Manuela Morleo; Michele Pinelli; Alessandra Varavallo; Manuel Posada De la Paz; Eva Bermejo Sánchez; Estrella López Martín; Beatriz Martínez Delgado; F. Javier Alonso García de la Rosa; Andrea Ciolfi; Bruno Dallapiccola; Simone Pizzi; Francesca Clementina Radio; Marco Tartaglia; Alessandra Renieri; Elisa Benetti; Peter Balicza; Maria Judit Molnar; Ales Maver; Borut Peterlin; Alexander Münchau; Katja Lohmann; Rebecca Herzog; Martje Pauly; Alfons Macaya; Anna Marcé-Grau; Andres Nascimiento Osorio; Daniel Natera de Benito; Rachel Thompson; Kiran Polavarapu; David Beeson; Judith Cossins; Pedro M. Rodriguez Cruz; Peter Hackman; Mridul Johari; Marco Savarese; Bjarne Udd; Rita Horvath; Gabriel Capella; Laura Valle; Elke Holinski-Feder; Andreas Laner; Verena Steinke-Lange; Evelin Schröck; Andreas Rump
HGG Advances, Vol 4, Iss 2, Pp 100186- (2023)
Academic Journal
Mosbah, H.; Donadille, B.; Vatier, C.; Janmaat, S.; Atlan, M.; Badens, C.; Barat, P.; Béliard, S.; Beltrand, J.; Ben Yaou, R.; Bismuth, E.; Boccara, F.; Cariou, B.; Chaouat, M.; Charriot, G.; Christin-Maitre, S.; De Kerdanet, M.; Delemer, B.; Disse, E.; Dubois, N.; Eymard, B.; Fève, B.; Lascols, O.; Mathurin, P.; Nobécourt, E.; Poujol-Robert, A.; Prevost, G.; Richard, P.; Sellam, J.; Tauveron, I.; Treboz, D.; Vergès, B.; Vermot-Desroches, V.; Wahbi, K.; Jéru, I.; Vantyghem, M. C.; Vigouroux, C.
Orphanet Journal of Rare Diseases. 17(Suppl 1)
Academic Journal
Perrin A; Laboratoire de Génétique Moléculaire, Centre Hospitalier Universitaire de Montpellier, Montpellier, France mireille.cossee@inserm.fr aurelien.perrin@ext.inserm.fr.; PhyMedExp, Université de Montpellier, INSERM, CNRS, Montpellier, France.; Métay C; Unité Fonctionnelle de Cardiogénétique et Myogénétique moléculaire et cellulaire, Centre de Génétique Moléculaire et Chromosomique, Groupe Hospitalier La Pitié-Salpêtrière-Charles Foix, Paris, France.; Sorbonne Université, INSERM, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.; Savarese M; Tampere Neuromuscular Center, Folkhälsan Research Center, Helsinki, Finland.; Ben Yaou R; Sorbonne Université, INSERM, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.; Demidov G; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tubingen, Germany.; Nelson I; Sorbonne Université, INSERM, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.; Solé G; CHU de Bordeaux, AOC National Reference Center for Neuromuscular Disorders, Bordeaux, France.; Péréon Y; Department of Clinical Neurophysiology, Reference Centre for Neuromuscular Diseases AOC, Filnemus, Euro-NMD, CHU Nantes, Nantes Université, Place Alexis-Ricordeau, Nantes, France.; Bertini ES; Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children Research Hospital, IRCCS, Rome, Italy.; Fattori F; Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children Research Hospital, IRCCS, Rome, Italy.; D'Amico A; Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children Research Hospital, IRCCS, Rome, Italy.; Ricci F; Division of Child and Adolescent Neuropsychiatry, University of Turin, Turin, Italy.; Ginsberg M; Department of Pediatric Neurology, Wolfson Medical Center, Holon, Israel.; Seferian A; Institut I-MOTION, Hôpital Armand Trousseau, Paris, France.; Boespflug-Tanguy O; Institut I-MOTION, Hôpital Armand Trousseau, Paris, France.; UMR 1141, INSERM, NeuroDiderot Université Paris Cité and APHP, Neuropédiatrie, French Reference Center for Leukodystrophies, LEUKOFRANCE, Hôpital Robert Debré, Paris, France.; Servais L; Institut I-MOTION, Hôpital Armand Trousseau, Paris, France.; MDUK Oxford Neuromuscular Centre & NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.; Neuromuscular Reference Center, Division of Paediatrics, University and Hospital University of Liège, Liège, Belgium.; Chapon F; Département de pathologie, Centre de Compétence des Maladies Neuromusculaires, Centre Hospitalier Universitaire de Caen, Caen, France.; Lagrange E; Centre de Compétences des Maladies Neuro Musculaires, Centre Hospitalier Universitaire Grenoble Alpes, Grenoble, France.; Gaudon K; Unité Fonctionnelle de Cardiogénétique et Myogénétique moléculaire et cellulaire, Centre de Génétique Moléculaire et Chromosomique, Groupe Hospitalier La Pitié-Salpêtrière-Charles Foix, Paris, France.; Bloch A; Unité Fonctionnelle de Cardiogénétique et Myogénétique moléculaire et cellulaire, Centre de Génétique Moléculaire et Chromosomique, Groupe Hospitalier La Pitié-Salpêtrière-Charles Foix, Paris, France.; Ghanem R; Unité Fonctionnelle de Cardiogénétique et Myogénétique moléculaire et cellulaire, Centre de Génétique Moléculaire et Chromosomique, Groupe Hospitalier La Pitié-Salpêtrière-Charles Foix, Paris, France.; Guyant-Maréchal L; Department of Neurophysiology, Rouen University Hospital, Rouen, France.; Johari M; Tampere Neuromuscular Center, Folkhälsan Research Center, Helsinki, Finland.; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Western Australia, Australia.; Van Goethem C; Laboratoire de Génétique Moléculaire, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; Montpellier BioInformatique pour le Diagnostic Clinique (MOBIDIC), Plateau de Médecine Moléculaire et Génomique (PMMG), CHU Montpellier, Montpellier, France.; Fardeau M; Sorbonne Université, INSERM, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.; Morales RJ; Department of Neurology, Hospital Universitario Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.; Genetti CA; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Marttila M; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; HiLIFE Helsinki Institute of Life Science, Tukholmankatu 8, FI-00014, University of Helsinki, Helsinki, Finland.; Koenig M; Laboratoire de Génétique Moléculaire, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; PhyMedExp, Université de Montpellier, INSERM, CNRS, Montpellier, France.; Beggs AH; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Udd B; Tampere Neuromuscular Center, Folkhälsan Research Center, Helsinki, Finland.; Bonne G; Sorbonne Université, INSERM, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.; Cossée M; Laboratoire de Génétique Moléculaire, Centre Hospitalier Universitaire de Montpellier, Montpellier, France mireille.cossee@inserm.fr aurelien.perrin@ext.inserm.fr.; PhyMedExp, Université de Montpellier, INSERM, CNRS, Montpellier, France.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Academic Journal
Cannie DE; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Syrris P; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Protonotarios A; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Bakalakos A; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Pruny JF; APHP, Sorbonne Université, Centre de Référence pour les Maladies Cardiaques Héréditaires ou rares, ICAN Institute, Hôpital Pitié-Salpêtrière, Paris, France.; Ditaranto R; Cardiology Unit, Cardiac Thoracic and Vascular Department, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Martinez-Veira C; Unidad de Cardiopatías Familiares, Complexo Hospitalario Universitario de A Coruña, Instituto de Investigación Biomédica de A Coruña (INIBIC/CIBERCV), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, A Coruña, Spain.; Larrañaga-Moreira JM; Unidad de Cardiopatías Familiares, Complexo Hospitalario Universitario de A Coruña, Instituto de Investigación Biomédica de A Coruña (INIBIC/CIBERCV), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, A Coruña, Spain.; Medo K; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Bermúdez-Jiménez FJ; Cardiology Department, Hospital Universitario Virgen de las Nieves, Instituto de Investigación Biosanitaria IBS Granada, Granada, Spain.; Ben Yaou R; APHP-Sorbonne Universite, Centre de Référence des Maladies Neuromusculaires, Inserm, Centre de Recherche en Myologie, Institut de Myologie, Hopital Pitie-Salpetriere, Paris, France.; Leturcq F; APHP, Cochin Hospital, Department of Genomic Medicine and Systemic Diseases, University of Paris, Paris, France.; Mezcua AR; Heart Failure and Familial Cardiomyopathies Unit, Department of Cardiology, IBIMA, Málaga. Spain.; Ciber-Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain.; Marini-Bettolo C; Department of Cardiology, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, UK.; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.; Cabrera E; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.; Reuter C; Stanford Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, 291 Campus Drive, Stanford, CA 94305, USA.; Limeres Freire J; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Ciber-Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain.; Inherited Cardiovascular Diseases Unit, Department of Cardiology, Hospital Universitari Vall d´Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.; Rodríguez-Palomares JF; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Ciber-Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain.; Inherited Cardiovascular Diseases Unit, Department of Cardiology, Hospital Universitari Vall d´Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.; Mestroni L; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Taylor MRG; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Parikh VN; Stanford Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, 291 Campus Drive, Stanford, CA 94305, USA.; Ashley EA; Stanford Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, 291 Campus Drive, Stanford, CA 94305, USA.; Barriales-Villa R; Unidad de Cardiopatías Familiares, Complexo Hospitalario Universitario de A Coruña, Instituto de Investigación Biomédica de A Coruña (INIBIC/CIBERCV), Servizo Galego de Saúde (SERGAS), Universidade da Coruña, A Coruña, Spain.; Jiménez-Jáimez J; Cardiology Department, Hospital Universitario Virgen de las Nieves, Instituto de Investigación Biosanitaria IBS Granada, Granada, Spain.; Garcia-Pavia P; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.; Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.; Charron P; APHP, Sorbonne Université, Centre de Référence pour les Maladies Cardiaques Héréditaires ou rares, ICAN Institute, Hôpital Pitié-Salpêtrière, Paris, France.; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; Biagini E; Cardiology Unit, Cardiac Thoracic and Vascular Department, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN-GUARDHEART).; García Pinilla JM; Heart Failure and Familial Cardiomyopathies Unit, Department of Cardiology, IBIMA, Málaga. Spain.; Ciber-Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain.; Departamento de Medicina y Dermatología, Universidad de Malaga, Malaga, Spain.; Bourke J; Department of Cardiology, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, UK.; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.; Savvatis K; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; William Harvey Institute, Queen Mary University London, London, United Kingdom.; National Institute for Health Research, University College London Hospitals Biomedical Research Centre, London, United Kingdom.; Wahbi K; AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.; AP-HP, Cochin Hospital, Cardiology Department, Paris Cedex, France.; Université de Paris, Paris, France; Paris Cardiovascular Research Center (PARCC), INSERM Unit 970, Paris, France.; Elliott PM; Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.
Publisher: Oxford University Press Country of Publication: England NLM ID: 8006263 Publication Model: Print Cited Medium: Internet ISSN: 1522-9645 (Electronic) Linking ISSN: 0195668X NLM ISO Abbreviation: Eur Heart J Subsets: MEDLINE
Electronic Resource
Ben Yaou, R; Yun, P; Dabaj, I; Norato, G; Donkervoort, S; Xiong, H; Nascimento, A; Maggi, L; Sarkozy, A; Monges, S; Bertoli, M; Komaki, H; Mayer, M; Mercuri, E; Zanoteli, E; Castiglioni, C; Marini-Bettolo, C; D'Amico, A; Deconinck, N; Desguerre, I; Erazo-Torricelli, R; Gurgel-Giannetti, J; Ishiyama, A; Kleinsteuber, KS; Lagrue, E; Laugel, V; Mercier, S; Messina, S; Politano, L; Ryan, MM; Sabouraud, P; Schara, U; Siciliano, G; Vercelli, L; Voit, T; Yoon, G; Alvarez, R; Muntoni, F; Pierson, TM; Gomez-Andres, D; Foley, AR; Quijano-Roy, S; Bonnemann, CG; Bonne, G
Academic Journal
Deconinck, N.; Dion, E.; Yaou, R. Ben; Ferreiro, A.; Eymard, B.; Briñas, L.; Payan, C.; Voit, T.; Guicheney, P.; Richard, P.; Allamand, V.; Bonne, G.; Stojkovic, T.
In Neuromuscular Disorders 2010 20(8):517-523
Academic Journal
Decostre, V.; Chikhaoui, C.; Vigouroux, C.; Behin, A.; Bassez, G.; Ferreiro, A.; Janmaat, S.; Masingue, M.; Stojkovic, T.; Vatier, C.; Quiles, R Villar; Roy, S Quijano; Wahbi, K.; Eymard, B.; Bonne, G.; Yaou, R Ben; Hogrel, J.
In Neuromuscular Disorders October 2023 33 Supplement 1:S159-S160
Academic Journal
Decostre, V.; Chikhaoui, C.; Vigouroux, C.; Behin, A.; Bassez, G.; Ferreiro, A.; Janmaat, S.; Masingue, M.; Stojkovic, T.; Vatier, C.; Quiles, R. Villar; Roy, S. Quijano; Wahbi, K.; Eymard, B.; Bonne, G.; Ben Yaou, R.; Hogrel, J.
Academic Journal
Atalaia, A.; Thompson, R.; Matalonga, L.; Hernandez-Ferrer, C.; Corvo, A.; Carmody, L.; Zurek, B.; Yaou, R Ben; Horvath, R.; Graessner, H.; Riess, O.; Robinson, P.; Lochmüller, H.; Beltran, S.; Bonne, G.
In Neuromuscular Disorders October 2023 33 Supplement 1:S142-S142
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