المؤلفون: Claudio Bruno, Gian Luca Vita, Jacqueline Montes, Maria Sframeli, Tina Duong, Valeria Sansone, Annalia Frongia, Mariacristina Scoto, John W. Day, Francesco Muntoni, Giorgia Coratti, Enrico Bertini, Jessica Exposito Escudero, Simona Lucibello, Marika Pane, Sonia Messina, Allan M. Glanzman, Eugenio Mercuri, Roberto De Sanctis, Elena S. Mazzone, Anna Mayhew, Laura Antonaci, Francesca Bovis, Andrés Nascimento Osorio, Matthew Civitello, Sara Carnicella, Rachel Salazar, Richard S. Finkel, Chiara Marini Bettolo, Adele D'Amico, Nathalie Goemans, Robert Muni Lofra, Darryl C. De Vivo, Marleen Van den Hauwe, Maria Carmela Pera, Evelin Milev, Amy Pasternak, Sally Dunaway Young, Emilio Albamonte, Basil T. Darras

المصدر: ANNALS OF NEUROLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Longitudinal study, Adolescent, Models, Neurological, Gene Dosage, Spinal Muscular Atrophies of Childhood, Young Adult, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, 0302 clinical medicine, Age of Onset, Child, Child, Preschool, Disease Progression, Female, Humans, Survival of Motor Neuron 2 Protein, Models, Internal medicine, medicine, Preschool, business.industry, Repeated measures design, Retrospective cohort study, Spinal muscular atrophy, medicine.disease, SMA, 030104 developmental biology, Neurology, Neurological, Cohort, Neurology (clinical), sma, Age of onset, business, 030217 neurology & neurosurgery, Cohort study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7eff96e16ed9ca4d83cccff947b5eecTest
https://doi.org/10.1002/ana.25900Test

المؤلفون: Rocio N, Villar-Quiles, Maja, von der Hagen, Corinne, Métay, Victoria, Gonzalez, Sandra, Donkervoort, Enrico, Bertini, Claudia, Castiglioni, Denys, Chaigne, Jaume, Colomer, Maria Luz, Cuadrado, Marianne, de Visser, Isabelle, Desguerre, Bruno, Eymard, Nathalie, Goemans, Angela, Kaindl, Emmanuelle, Lagrue, Jürg, Lütschg, Edoardo, Malfatti, Michèle, Mayer, Luciano, Merlini, David, Orlikowski, Ulrike, Reuner, Mustafa A, Salih, Beate, Schlotter-Weigel, Mechthild, Stoetter, Volker, Straub, Haluk, Topaloglu, J Andoni, Urtizberea, Anneke, van der Kooi, Ekkehard, Wilichowski, Norma B, Romero, Michel, Fardeau, Carsten G, Bönnemann, Brigitte, Estournet, Pascale, Richard, Susana, Quijano-Roy, Ulrike, Schara, Ana, Ferreiro

المصدر: Neurology

مصطلحات موضوعية: Adult, Male, Adolescent, Genotype, Muscle Proteins, Middle Aged, Article, Young Adult, Muscular Diseases, Child, Preschool, Humans, Female, Child, Selenoproteins, Follow-Up Studies, Retrospective Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::e88560683abbf952be2edde6fc9cd071Test
https://pubmed.ncbi.nlm.nih.gov/32796131Test

المؤلفون: Hilde Van Esch, Luc Dehaspe, Kristl G. Claeys, Joris Vermeesch, Nathalie Goemans, Thomy de Ravel, Kris Van Den Bogaert, Valerie Race, Hilde Peeters, Eric Legius, Jazz Storms, Koenraad Devriendt, Nathalie Brison, Darine Villela, Liesbeth De Waele

المساهمون: Medical Genetics

مصطلحات موضوعية: 0301 basic medicine, Adult, congenital, hereditary, and neonatal diseases and abnormalities, DNA Copy Number Variations, endocrine system diseases, Noninvasive Prenatal Testing, Population, Sequence Analysis, DNA/ethics, 030105 genetics & heredity, DNA Copy Number Variations/genetics, Noninvasive Prenatal Testing/ethics, Dystrophin, 03 medical and health sciences, Prenatal Diagnosis, Prenatal Diagnosis/ethics, mental disorders, medicine, Humans, Copy-number variation, education, Genetics (clinical), Genetics, Dystrophin/genetics, Pregnancy, education.field_of_study, Incidental Findings, business.industry, Sequence Analysis, DNA, medicine.disease, Pathogenicity, fetus, NIPS, 030104 developmental biology, Prenatal screening, Dmd gene, secondary findings, Female, pregnancy, business, DMD gene, maternal CNV

وصف الملف: Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b58ddfaa22b0a77211f3e82a0ce36e8Test
https://lirias.kuleuven.be/handle/123456789/638443Test

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

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

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

المؤلفون: Johan L.K. Van Hove, Tony Reybrouck, Patrice Givron, Ann Meulemans, Sara Seneca, Joél Smet, Nathalie Goemans, Raphael Sciot, Rudy Van Coster

المساهمون: Department of Embryology and Genetics

المصدر: Vrije Universiteit Brussel

مصطلحات موضوعية: Adult, Mitochondrial DNA, Biopsy, DNA Mutational Analysis, Molecular Sequence Data, mitochondrial DNA, Mitochondrion, Biology, medicine.disease_cause, tRNA genes, DNA, Mitochondrial, Mitochondrial myopathy, Genetics, medicine, Humans, Point Mutation, Muscle, Skeletal, Genetics (clinical), RNA, Transfer, Asp, Mutation, Muscle biopsy, Base Sequence, medicine.diagnostic_test, Point mutation, mitochondrial myopathy, Mitochondrial Myopathies, exercise intolerance, medicine.disease, Molecular biology, Heteroplasmy, Biochemistry, Transfer RNA, tRNAAsp, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359b88304805283e61a6e85d64c57709Test
https://doi.org/10.1002/ajmg.a.30854Test

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 DISEASES

مصطلحات 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

المؤلفون: R. de Vries, S Stein, R. De Sanctis, Concetta Palermo, Maria Pia Sormani, M. Vigo, Enrico Bertini, Alessandra D'Amico, M. de Visser, Nathalie Goemans, Francesco Muntoni, J. Fagoaga Mata, Marion Main, M. van den Hauwe, Rudolf Korinthenberg, Eugenio Mercuri, Lavinia Fanelli, M. Eagle, Flaviana Bianco, Marika Pane, Mariacristina Scoto, M. Ash, A. Febrer, Elena S. Mazzone, Anna Mayhew, K. Bushby

المساهمون: Neurology

المصدر: Neuromuscular disorders, 23(8), 624-628. Elsevier Limited

مصطلحات موضوعية: Adult, Male, Longitudinal study, Pediatrics, medicine.medical_specialty, SIX MINUTE WALK, Type III Spinal Muscular Atrophy, Adolescent, Adult, Analysis of Variance, Atrophy, Child, Child, Preschool, Exercise Test, Exercise Therapy, methods, Female, Humans, International Cooperation, Longitudinal Studies, Male, Middle Aged, Outcome Assessment (Health Care), Spinal Muscular Atrophies of Childhood, etiology/rehabilitation, Walking, Young Adult, Adolescent, International Cooperation, Walking, Spinal Muscular Atrophies of Childhood, Outcome measures, methods, Outcome Assessment (Health Care), Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Atrophy, 6MWT, Outcome Assessment, Health Care, medicine, Humans, Longitudinal Studies, Young adult, Preschool, Child, Genetics (clinical), Analysis of Variance, business.industry, Spinal muscular atrophy, Middle Aged, medicine.disease, SMA, Exercise Therapy, Neurology, Child, Preschool, Pediatrics, Perinatology and Child Health, Cohort, Exercise Test, Physical therapy, Female, Neurology (clinical), Analysis of variance, business, etiology/rehabilitation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c28b0885e826eef9c20cfb90fb33370aTest
https://pure.amc.nl/en/publications/six-minute-walk-test-in-type-iii-spinal-muscular-atrophy-a-12month-longitudinal-studyTest(46d0387e-3610-415d-b857-1ee944de2dcd).html

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