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المؤلفون: Sonia Messina, Claudio Bruno, E. Mazzone, Eugenio Mercuri, Valeria A. Sansone, Claudia Brogna, Gianluca Vita, Francesco Muntoni, Marika Pane, Tiziana Mongini, Giovanni Baranello, Erik H. Niks, Mary Chesshyre, Francesca Magri, Volker Straub, Enrico Bertini, Elena Pegoraro, Luca Bello, Alice Donati, Silvana De Lucia, Stefano C. Previtali, Valeria Ricotti, Adele D'Amico, Jean-Yves Hogrel, Nathalie Goemans, Roberta Battini, Giacomo P. Comi, Laurent Servais, Giorgia Coratti, Federica Ricci, Imelda J. M. de Groot, Luisa Politano, Angela Berardinelli
المصدر: PLoS ONE, 16(6). PUBLIC LIBRARY SCIENCE
PLoS ONE
PLoS ONE, Vol 16, Iss 6, p e0253882 (2021)مصطلحات موضوعية: Male, Heredity, Genetic Linkage, Epidemiology, Physiology, Duchenne muscular dystrophy, Walking, Duchenne Muscular Dystrophy, Severity of Illness Index, Muscular Dystrophies, Dystrophin, Exon, 0302 clinical medicine, Medical Conditions, Medicine and Health Sciences, 030212 general & internal medicine, Muscular Dystrophy, Longitudinal Studies, Child, Baseline values, Multidisciplinary, Settore MED/48 - SCIENZE INFERMIERISTICHE E TECNICHE NEURO-PSICHIATRICHE E RIABILITATIVE, Organic Compounds, Men, Exons, Multidisciplinary Sciences, Chemistry, Deletion Mutation, Neurology, X-Linked Traits, Sex Linkage, Ambulatory, Physical Sciences, Disease Progression, Medicine, Science & Technology - Other Topics, Steroids, exon skipping, Research Article, medicine.medical_specialty, Science, Natural history of disease, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Internal medicine, medicine, Genetics, Humans, Clinical Genetics, Science & Technology, business.industry, Biological Locomotion, Organic Chemistry, Chemical Compounds, Biology and Life Sciences, Human Genetics, medicine.disease, Duchenne, Human genetics, Exon skipping, Follow-Up Studies, Muscular Dystrophy, Duchenne, Mutation, Clinical trial, Natural History of Disease, Medical Risk Factors, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf; Electronic-eCollection
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de7208ef0a5c3984e1eb8d2853199ed7Test
http://hdl.handle.net/1887/3249481Test -
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المؤلفون: Craig M. McDonald, Kathryn R. Wagner, Erica Koenig, Jyoti Malhotra, Navid Khan, Perry B. Shieh, Promovi Trial Clinical Investigators, Baoguang Han, Hoda Z. Abdel-Hamid, Anne M. Connolly, Nathalie Goemans, Wenfei Zhang, Emma Ciafaloni, Eugenio Mercuri, Jerry R. Mendell
المصدر: Journal of Neuromuscular Diseases
مصطلحات موضوعية: Male, Research Report, 0301 basic medicine, safety, medicine.medical_specialty, Adolescent, Duchenne muscular dystrophy, Vital Capacity, Clinical Neurology, Eteplirsen, Morpholinos, Dystrophin, 03 medical and health sciences, 0302 clinical medicine, treatment efficacy, Internal medicine, medicine, Humans, Muscular dystrophy, Child, Adverse effect, Science & Technology, biology, business.industry, duchenne, Neurosciences, clinical trial, Exons, medicine.disease, Duchenne, Exon skipping, Muscular Dystrophy, Duchenne, Clinical trial, AMBULATION, 030104 developmental biology, Neurology, phase 3, Mutation, Cohort, Disease Progression, biology.protein, Neurology (clinical), Neurosciences & Neurology, business, Life Sciences & Biomedicine, 030217 neurology & neurosurgery
وصف الملف: Print
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d98e1fd113eb9e7f0a3d44bbc526d535Test
https://lirias.kuleuven.be/handle/20.500.12942/706497Test -
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المؤلفون: Nathalie Goemans, Brenda Wong, Marleen Van den Hauwe, James Signorovitch, Gautam Sajeev, David Cox, John Landry, Madeline Jenkins, Ibrahima Dieye, Zhiwen Yao, Intekhab Hossain, Susan J Ward, Collaborative Trajectory Analysis Project (cTAP)
المصدر: PLoS ONE, Vol 15, Iss 6, p e0232870 (2020)
PLoS ONEمصطلحات موضوعية: 0301 basic medicine, Male, Heredity, Physiology, Genetic Linkage, Duchenne muscular dystrophy, Walking, Duchenne Muscular Dystrophy, 030105 genetics & heredity, Pediatrics, Muscular Dystrophies, DISEASE, law.invention, Tadalafil, Efficacy, 0302 clinical medicine, Randomized controlled trial, DESIGN, law, Medicine and Health Sciences, Medicine, Child, Multidisciplinary, Organic Compounds, Prognosis, Phase III clinical investigation, Multidisciplinary Sciences, Chemistry, Neurology, Neuromuscular Agents, X-Linked Traits, Sex Linkage, Ambulatory, Physical Sciences, Disease Progression, Science & Technology - Other Topics, Steroids, TRIAL, Research Article, medicine.medical_specialty, Drug Research and Development, Adolescent, Science, ATALUREN, Placebo, Research and Analysis Methods, 03 medical and health sciences, DRISAPERSEN, Diagnostic Medicine, Genetics, Humans, Clinical Trials, Computer Simulation, Clinical Genetics, Pharmacology, Science & Technology, business.industry, Biological Locomotion, Clinical study design, Organic Chemistry, Chemical Compounds, Biology and Life Sciences, medicine.disease, Clinical trial, Muscular Dystrophy, Duchenne, Sample size determination, Sample Size, Physical therapy, Exercise Test, Clinical Medicine, business, 030217 neurology & neurosurgery, Follow-Up Studies
وصف الملف: Electronic-eCollection
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c05aa276ab26d60ebede754c9790ea90Test
https://lirias.kuleuven.be/handle/20.500.12942/704020Test -
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المؤلفون: Nathalie Goemans, Annemieke Aartsma-Rus
مصطلحات موضوعية: 0301 basic medicine, Duchenne muscular dystrophy, medicine.medical_specialty, Eteplirsen, Biochemistry, Morpholinos, Food and drug administration, 03 medical and health sciences, 0302 clinical medicine, Government Agencies, Drug Discovery, Genetics, Medicine, Humans, Molecular Biology, Drug Approval, clinical trials, business.industry, United States Food and Drug Administration, Negative opinion, United States, Clinical trial, Europe, Muscular Dystrophy, Duchenne, 030104 developmental biology, regulatory approval, 030220 oncology & carcinogenesis, Family medicine, Molecular Medicine, Patient representatives, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26193b2810925a0807833f8732e75c7bTest
https://hdl.handle.net/1887/88325Test -
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المؤلفون: S. de Kimpe, D. de Klerk, Monika Hiller, Jan J.G.M. Verschuuren, Annemieke Aartsma-Rus, R. Jean-Baptiste, Francesco Muntoni, Mar Tulinius, Afrodite Lourbakos, Peter Nilsson, Zaïda Koeks, K. Kozaczynska, G. Campion, Nathalie Goemans, Pietro Spitali, Burcu Ayoglu, Ron Wolterbeek, Vishna Devi Nadarajah, N. Yau, Peter A C 't Hoen, Erik H. Niks, Mojgan Reza, Hanns Lochmüller, P. de Bruijn, C. Al-Khalili Szigyarto, Irina Zaharieva
المصدر: Scientific Reports
Scientific Reports, 7
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, Male, medicine.medical_specialty, Adolescent, government.form_of_government, Duchenne muscular dystrophy, Placebo-controlled study, lcsh:Medicine, Muscle disorder, Article, Dystrophin, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Double-Blind Method, Internal medicine, Medicine, Humans, Longitudinal Studies, Muscular dystrophy, lcsh:Science, Child, Drisapersen, Randomized Controlled Trials as Topic, Antisense therapy, Multidisciplinary, biology, business.industry, lcsh:R, Exons, Oligonucleotides, Antisense, medicine.disease, Clinical trial, Muscular Dystrophy, Duchenne, 030104 developmental biology, Clinical Trials, Phase III as Topic, Matrix Metalloproteinase 9, Child, Preschool, government, biology.protein, lcsh:Q, Female, business, 030217 neurology & neurosurgery, Biomarkers
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e00690df27119c632541d5bb3e76d3aTest
https://hdl.handle.net/1887/115152Test -
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المؤلفون: Janbernd Kirschner, S. Fontaine-Carbonnel, Giuseppe Vita, Enrico Bertini, François Rivier, Nathalie Goemans, W. Ludo van der Pol, Mariacristina Scoto, Brigitte Chabrol, Carole Vuillerot, Helen Roper, Alessandra Govoni, Maggie C. Walter, Jeppe Buchbjerg, Anna Lusakowska, Ulrike Schara, Eugenio Mercuri, Jean Louis Abitbol, Thomas Blaettler, Nicolas Deconinck, Michela Guglieri, Eduardo Vianna, Claudio Bruno, Jean Marie Cuisset, Francesco Muntoni, Carol Reid, Eric Dessaud, Hanns Lochmüller, Giacomo P. Comi, Brigitte Estournet, Patricia Sanwald Ducray, Carole André, Francesca Magri, Bruno Scherrer, Leonard H. van den Berg, Paulo Fontoura, Ksenija Gorni, Wolfgang Müller-Felber, Michèle Mayer
المساهمون: Schara, Ulrike (Beitragende*r)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Adolescent, Population, Medizin, Phases of clinical research, Spinal Muscular Atrophies of Childhood, Placebo, law.invention, 03 medical and health sciences, chemistry.chemical_compound, Young Adult, Outcome Assessment (Health Care), 0302 clinical medicine, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Randomized controlled trial, Double-Blind Method, law, Outcome Assessment, Health Care, Clinical endpoint, medicine, Humans, Mobility Limitation, education, Adverse effect, Child, Preschool, Cholestenones, education.field_of_study, business.industry, Child, Preschool, Female, Neuroprotective Agents, Neurology (clinical), Clinical trial, 030104 developmental biology, chemistry, N/A, Olesoxime, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bad810ec4902101d89d04fe23c17c79Test
http://hdl.handle.net/11570/3114831Test -
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المؤلفون: A. Johnson, Eugenio Mercuri, G. Campion, Robert Hemmings, Elizabeth Vroom, Edward M. Kaye, Nathalie Goemans, Virginia Arechavala-Gomeza, Bruno Sepodes, Annemieke Aartsma-Rus, Pavel Balabanov, Manuel Haas, Francesco Muntoni, Pat Furlong, Monica Ensini, Annamaria De Luca, Erik H. Niks, Aurélie Goyenvalle, Alejandra Pereda, O. Veldhuizen, Kate Bushby, Matthew J.A. Wood, Violeta Stoyanova-Beninska, Volker Straub
المصدر: ResearcherID
CIÊNCIAVITAE
The Lancet Neurology, 15(8), 882-890مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Orphan Drug Production, Duchenne muscular dystrophy, Alternative medicine, Disease, Public-Private Sector Partnerships, 03 medical and health sciences, 0302 clinical medicine, Health care, Outcome Assessment, Health Care, medicine, Humans, Muscular dystrophy, Intensive care medicine, Drug Approval, business.industry, Stakeholder, Genetic Therapy, medicine.disease, Clinical trial, Muscular Dystrophy, Duchenne, Settore MED/26 - NEUROLOGIA, 030104 developmental biology, Physical therapy, Neurology (clinical), business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11c0cb8b87625fffd262a4ed459b000bTest
https://hdl.handle.net/1887/112654Test -
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المؤلفون: Elyse Swallow, Collaborative Trajectory Analysis, Marleen Van den Hauwe, James Signorovitch, Jinlin Song, Nathalie Goemans
المصدر: PLoS ONE
PLoS ONE, Vol 11, Iss 10, p e0164684 (2016)مصطلحات موضوعية: Male, Heredity, Supine position, Physiology, Genetic Linkage, Epidemiology, Duchenne muscular dystrophy, Walking, Duchenne Muscular Dystrophy, Biochemistry, Muscular Dystrophies, Standard deviation, Dystrophin, Mathematical and Statistical Techniques, 0302 clinical medicine, Medicine and Health Sciences, Biomechanics, Child, Multidisciplinary, Organic Compounds, Age Factors, Prognosis, Explained variation, Chemistry, Neurology, X-Linked Traits, Sex Linkage, Child, Preschool, 030220 oncology & carcinogenesis, Physical Sciences, Ambulatory, Medicine, Steroids, Statistics (Mathematics), Research Article, medicine.medical_specialty, Drug Research and Development, Adolescent, Genotype, Science, Research and Analysis Methods, Natural history of disease, 03 medical and health sciences, Diagnostic Medicine, Genetics, medicine, Humans, Clinical Trials, Statistical Methods, Clinical Genetics, Pharmacology, Biological Locomotion, business.industry, Organic Chemistry, Chemical Compounds, Biology and Life Sciences, Proteins, Repeated measures design, Models, Theoretical, medicine.disease, Muscular Dystrophy, Duchenne, Clinical trial, Cytoskeletal Proteins, Natural History of Disease, Exercise Test, Physical therapy, Clinical Medicine, business, Mathematics, 030217 neurology & neurosurgery, Follow-Up Studies, Forecasting
وصف الملف: Electronic-eCollection; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::549f2e150970d8e439ec6a09f9e507a6Test
http://dx.plos.org/10.1371/journal.pone.0164684Test -
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المؤلفون: Anna-Karin Kroksmark, G. Campion, Judith C. van Deutekom, Marleen Van den Hauwe, R. Wilson, Mar Tulinius, Nathalie Goemans, Afrodite Lourbakos, Sjef J. de Kimpe, Gunnar Buyse
المصدر: PLoS ONE, Vol 11, Iss 9, p e0161955 (2016)
PLoS ONEمصطلحات موضوعية: Male, 0301 basic medicine, Heredity, Muscle Physiology, Muscle Functions, Physiology, Genetic Linkage, Epidemiology, Biopsy, Duchenne muscular dystrophy, Oligonucleotides, Walking, Duchenne Muscular Dystrophy, Biochemistry, Muscular Dystrophies, Dystrophin, 0302 clinical medicine, Medicine and Health Sciences, Biomechanics, Muscular dystrophy, Child, Routes of Administration, Multidisciplinary, Treatment Outcome, Neurology, X-Linked Traits, Sex Linkage, Child, Preschool, Anesthesia, Cohort, Medicine, Research Article, medicine.medical_specialty, Adolescent, Science, Surgical and Invasive Medical Procedures, 03 medical and health sciences, Pharmacokinetics, Genetics, medicine, Humans, Dosing, Muscle, Skeletal, Adverse effect, Drisapersen, Pharmacology, Clinical Genetics, Biological Locomotion, business.industry, Biology and Life Sciences, Proteins, medicine.disease, Surgery, Muscular Dystrophy, Duchenne, Clinical trial, Cytoskeletal Proteins, Natural History of Disease, 030104 developmental biology, Subcutaneous Injections, Exercise Test, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a66d854fa2a6a9623e3f001f154722dTest
https://doi.org/10.1371/journal.pone.0161955Test -
10
المؤلفون: Adele D'Amico, Serena Sivo, Mariacristina Scoto, Nathalie Goemans, Maria Pia Sormani, Rachel Salazar, Janet Quigley, Gian Luca Vita, Jacqueline Montes, Francesco Muntoni, Richard S. Finkel, Eugenio Mercuri, Petra Kaufmann, Sonia Messina, Enrico Bertini, Marika Pane, Danielle Ramsey, Darryl C. De Vivo, Maria Carmela Pera, Amy Pasternak, Allan M. Glanzman, Elena S. Mazzone, Anna Mayhew, Maria Sframeli, Marion Main, Sally Dunaway, Basil T. Darras, Marleen Van den Hauwe
المصدر: ResearcherID
Neuromuscular Disordersمصطلحات موضوعية: 0301 basic medicine, Male, Hammersmith Functional Motor Scale, Outcome measures, Spinal muscular atrophy, Neurology (clinical), Pediatrics, Perinatology and Child Health, Genetics (clinical), Neurology, 030105 genetics & heredity, Spinal Muscular Atrophies of Childhood, Pediatrics, 0302 clinical medicine, Adolescent, Adult, Child, Child, Preschool, Clinical Trials as Topic, Female, Humans, Middle Aged, Retrospective Studies, Young Adult, Disease Progression, Mobility Limitation, Medicine, Genetics(clinical), Young adult, Baseline values, Perinatology and Child Health, SMA, medicine.medical_specialty, Clinical Neurology, Article, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Age groups, Internal medicine, Pediatrics, Perinatology, and Child Health, Preschool, business.industry, Disease progression, Retrospective cohort study, Large cohort, Clinical trial, Physical therapy, business, 030217 neurology & neurosurgery
وصف الملف: Print-Electronic
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http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000371652100002&KeyUID=WOS:000371652100002Test