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المؤلفون: Monique M. Ryan, Craig Campbell, Juan J. Vílchez, Brigitte Chabrol, Panayiota Trifillis, Joseph McIntosh, Mar Tulinius, Eugenio Mercuri, Stuart W. Peltz, Kristi J. Jones, Yann Péreón, Basil T. Darras, Thomas Sejersen, Giacomo P. Comi, Kathryn Selby, Jean K. Mah, Marcio Souza, Enrico Bertini, Thomas Voit, Brenda L. Wong, Nathalie Goemans, Francesco Muntoni, Ulrike Schara, Jacinda B. Sampson, Susan T. Iannaccone, Gary Elfring, Janbernd Kirschner, Craig M. McDonald, Yoram Nevo, Lee-Jen Wei, Richard S. Finkel, J. Ben Renfroe, Katherine D. Mathews, Richard J. Barohn, Kevin M. Flanigan
المصدر: Paediatrics Publications
مصطلحات موضوعية: Duchenne muscular dystrophy, medicine.medical_specialty, nonsense mutation Duchenne muscular dystrophy, Nonsense mutation, efficacy, MULTICENTER, Medizin, Placebo, law.invention, Efficacy, 03 medical and health sciences, chemistry.chemical_compound, 6-MINUTE WALK TEST, 0302 clinical medicine, Randomized controlled trial, law, Internal medicine, END-POINTS, medicine, Humans, Muscular Dystrophy, Muscular dystrophy, Codon, 030304 developmental biology, Randomized Controlled Trials as Topic, 0303 health sciences, Oxadiazoles, Science & Technology, business.industry, Health Policy, ataluren, medicine.disease, Duchenne, Ataluren, Muscular Dystrophy, Duchenne, 6-minute walk distance, Health Care Sciences & Services, chemistry, Nonsense, meta-analyses, Codon, Nonsense, Ambulatory, randomized controlled trials, business, Life Sciences & Biomedicine, 030217 neurology & neurosurgery
وصف الملف: Print-Electronic; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::921c77381755297d0bab3f2e9a88f720Test
https://pubmed.ncbi.nlm.nih.gov/32851872Test -
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المؤلفون: Sofie Symoens, Riet De Rycke, Nathalie Goemans, Delfien Syx, Tibbe Dhooge, Anne Destree, Fransiska Malfait, Florence Petit, Sarah Delbaere, Olivier Vanakker
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 22(1)
مصطلحات موضوعية: Adult, Collagen Type XII, Male, Adolescent, Decorin, Collagen Type VI, Compound heterozygosity, Tenascin X, Extracellular matrix, Muscular Diseases, Protein Domains, Collagen VI, medicine, Humans, Child, Genetics (clinical), Cells, Cultured, biology, High-Throughput Nucleotide Sequencing, Tenascin, Sequence Analysis, DNA, medicine.disease, Molecular biology, Exon skipping, Extracellular Matrix, Pedigree, Fibronectin, Ehlers–Danlos syndrome, Child, Preschool, Mutation, biology.protein, Ehlers-Danlos Syndrome, Female, Collagen Type V
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7dab76dd98e837602a64e4f4f0320f7Test
https://pubmed.ncbi.nlm.nih.gov/31273343Test -
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المؤلفون: Christine Wittevrongel, Nathalie Goemans, Veerle Labarque, Marc Hoylaerts, Rita Vos, Chris Van Geet, Chantal Thys, Kathleen Freson
المصدر: Human Molecular Genetics. 17:357-366
مصطلحات موضوعية: Blood Platelets, Male, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Gs alpha subunit, Cytoskeleton organization, Duchenne muscular dystrophy, Blood Loss, Surgical, In Vitro Techniques, Dystrophin, Extracellular matrix, Von Willebrand factor, Laminin, Internal medicine, GTP-Binding Protein alpha Subunits, Gs, Genetics, medicine, Humans, Platelet, Child, Molecular Biology, Cytoskeleton, Genetics (clinical), biology, General Medicine, Platelet Activation, medicine.disease, Muscular Dystrophy, Duchenne, Spinal Fusion, Endocrinology, Case-Control Studies, Mutation, biology.protein, Collagen, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1091c5b84531e98de52d17c5e3fde29bTest
https://doi.org/10.1093/hmg/ddm312Test -
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المؤلفون: Nathalie Goemans, Matthias Mörgelin, Kathryn N. North, Rachel A. Peat, Shireen R. Lamandé, John F. Bateman, Naomi L. Baker
المساهمون: University of Groningen
المصدر: Human Molecular Genetics, 14(2), 279-293. Oxford University Press
مصطلحات موضوعية: Adult, IN-FRAME DELETION, VONWILLEBRAND-FACTOR, TRIPLE-HELIX, Ullrich congenital muscular dystrophy, BETHLEM-MYOPATHY, ENDOPLASMIC-RETICULUM, Genes, Recessive, Collagen Type VI, Biology, medicine.disease_cause, Compound heterozygosity, Muscular Dystrophies, MICROFIBRIL FORMATION, Collagen VI, Genetics, medicine, Humans, RNA, Messenger, Child, Molecular Biology, Genetics (clinical), Genes, Dominant, Mutation, MESSENGER-RNA DECAY, Bethlem myopathy, Infant, Muscle weakness, Heterozygote advantage, GLOBULAR DOMAINS, General Medicine, Fibroblasts, medicine.disease, OLIGOMERIZATION DOMAINS, Osteogenesis imperfecta, OSTEOGENESIS IMPERFECTA, Child, Preschool, Microfibrils, medicine.symptom
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b4662eafe749a2b675730bdf29b58fcTest
https://research.rug.nl/en/publications/30a9d54f-1af2-4fc3-bc4a-2dadd46b6394Test -
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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 -
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المؤلفون: Fransiska Malfait, Anne De Paepe, Sheela Nampoothiri, Yolanda Gyftodimou, Vanesa López-González, Michael B. Petersen, Nathalie Goemans, Geert Mortier, Sofie Symoens, Eva Holmberg
المصدر: Orphanet journal of rare diseases
Malfait, F, Symoens, S, Goemans, N, Gyftodimou, Y, Holmberg, E, López-González, V, Mortier, G, Nampoothiri, S, Petersen, M B & De Paepe, A 2013, ' Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome ', Orphanet Journal of Rare Diseases, vol. 8, pp. 78 . https://doi.org/10.1186/1750-1172-8-78Test
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASESمصطلحات موضوعية: Male, COL1A2, ADULTHOOD, DOMAIN, Arterial fragility, Medicine and Health Sciences, Genetics(clinical), Pharmacology (medical), Child, Genetics (clinical), Medicine(all), ARTHROCHALASIA TYPE, Fibrillogenesis, Procollagen N-Endopeptidase, Overlap syndrome, General Medicine, Osteogenesis Imperfecta, Phenotype, Osteogenesis imperfecta, END, Female, medicine.symptom, Type I collagen, Procollagen, Adult, medicine.medical_specialty, Genotype, PROCOLLAGEN N-PROTEINASE, Short stature, Collagen Type I, Internal medicine, medicine, Humans, business.industry, Research, Biology and Life Sciences, medicine.disease, GENE, VIIA, Peptide Fragments, Collagen Type I, alpha 1 Chain, Procollagen peptidase, Endocrinology, DEFECT, Ehlers–Danlos syndrome, Mutation, CHAIN, Ehlers-Danlos Syndrome, Human medicine, business
وصف الملف: pdf; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca3d0d8c88ea8ee888d4486667a3888Test
https://hdl.handle.net/10067/1090000151162165141Test -
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المؤلفون: Nathalie Goemans, Erik Gerlo, Elena Levtchenko, Geert A. Martens, Rita Vos, Jaak Jaeken, Chris Van Geet, Gunnar M. Buyse, Chantal Thys, Michela Di Michele, Kathleen Freson, Christophe Goubau
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 15(1)
مصطلحات موضوعية: Adult, Blood Platelets, Glycerol, Male, medicine.medical_specialty, Adolescent, Aquaporin, Biology, medicine.disease_cause, Aquaporins, Young Adult, Internal medicine, medicine, Humans, Child, Codon, Genetics (clinical), Mutation, Aquaporin 3, Homozygote, Infant, Amino acid substitution, Middle Aged, Transport protein, Pedigree, Protein Transport, Endocrinology, Amino Acid Substitution, Platelet secretion, Child, Preschool, Female, Blood Platelet Disorders
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43fae7fcc523bb826d47f30b65bef82fTest
https://pubmed.ncbi.nlm.nih.gov/22899094Test -
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المؤلفون: Radim Mazanec, Nathalie Goemans, Albena Jordanova, H.-J. Christen, Christine Verellen, James R. Lupski, Jan De Bleecker, Paolo Vinci, Matthias Van Hul, Kristien Verhoeven, Rudy Van Coster, Els De Vriendt, Andrzej Kochański, Wim Robberecht, Jeffery M. Vance, Velina Guergueltcheva, Peter De Jonghe, Ian J. Butler, Gulam Mustafa Saifi, Peter Vieregge, Vedrana Milic Rasic, Filip Roelens, J. Michael Schröder, Eva Nelis, Chantal Ceuterick, Kristl Claeys, Pavel Seeman, Kinga Szigeti, Barbara Ryniewicz, Pedro Mancias, Stephan Züchner, Yoram Nevo, I. Tournev, Vincent Timmerman, María Teresa García Moreno, Michaela Auer-Grumbach, Joachim Weis, Peter Van den Bergh, Michael E. Shy
المصدر: Brain
مصطلحات موضوعية: Pathology, medicine.disease_cause, Severity of Illness Index, GTP Phosphohydrolases, 0302 clinical medicine, Degenerative disease, Charcot-Marie-Tooth Disease, Genotype, mitofusin 2, Age of Onset, Child, 0303 health sciences, Mutation, education.field_of_study, Middle Aged, Electrophysiology, medicine.anatomical_structure, Phenotype, Child, Preschool, Sensory nerve, Adult, medicine.medical_specialty, Adolescent, Population, Sural nerve, Biology, genotype-phenotype correlation, Mitochondrial Proteins, 03 medical and health sciences, Atrophy, atrophy, Sural Nerve, medicine, features, Humans, education, gene, 030304 developmental biology, Aged, Membrane Proteins, medicine.disease, charcot-marie-tooth type 2, mitofusin-2, Surgery, Microscopy, Electron, disease type-2, neuropathy, Neurology (clinical), Age of onset, 030217 neurology & neurosurgery
وصف الملف: Print-Electronic; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fbd19685d12f10b9f298f3ffdd049b5Test
https://pubmed.ncbi.nlm.nih.gov/16714318Test -
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المؤلفون: Liese Verstraete, Hilde Feys, Katrijn Klingels, Charlotte Peeters, Marleen Van den Hauwe, Gunnar Buyse, Nathalie Goemans, Stefanie Boons
المساهمون: Schuelke, Markus
المصدر: PLoS ONE
PLoS ONE, Vol 8, Iss 12, p e84120 (2013)مصطلحات موضوعية: Male, Percentile, medicine.medical_specialty, Anatomy and Physiology, Science, Population, Walking, Developmental and Pediatric Neurology, Social and Behavioral Sciences, Pediatrics, Muscular Dystrophies, Child Development, Predictive Value of Tests, Reference Values, Outcome Assessment, Health Care, Humans, Medicine, Sports and Exercise Medicine, Exercise physiology, Child, education, Musculoskeletal System, Exercise, education.field_of_study, Models, Statistical, Multidisciplinary, Anthropometry, business.industry, Age Factors, Neuromuscular Diseases, Test (assessment), Muscular Dystrophy, Duchenne, Neurology, Anthropology, Child, Preschool, Predictive value of tests, Reference values, Ambulatory, Exercise Test, Physical therapy, Physiotherapy and Rehabilitation, Physical Anthropology, business, Research Article
وصف الملف: Electronic-eCollection
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0c25a0a7d454c409bf86723cbcfdda7Test
https://doi.org/10.1371/journal.pone.0084120Test -
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المصدر: Journal of Pediatric Gastroenterology & Nutrition. 57:e19
مصطلحات موضوعية: Glycerol, Male, Genetics, business.industry, Gastroenterology, MEDLINE, Aquaporin, Gene mutation, Pediatrics, Perinatology and Child Health, Humans, Medicine, Female, Hemochromatosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89507a61f6f12cc30d1b1d5d8f13ac7aTest
https://doi.org/10.1097/mpg.0b013e31829a4ff3Test
