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1
المؤلفون: Valeria A. Sansone, Matthew Civitello, Mariacristina Scoto, Adele D'Amico, Emilio Albamonte, Irene Mizzoni, Anna Lia Frongia, Maria Carmela Pera, Basil T. Darras, John W. Day, Amy Pasternak, Francesca Bovis, Sally Dunaway Young, Giorgia Coratti, Laura Antonaci, Eugenio Mercuri, Maria Sframeli, Tina Duong, Claudio Bruno, Annemarie Rohwer, Jacqueline Montes, Richard S. Finkel, Marika Pane, Darryl C. De Vivo, Enrico Bertini, Giovanni Baranello, Evelin Milev, Roberto De Sanctis, Francesco Muntoni, Sonia Messina, Allan M. Glanzman, Elena S. Mazzone, Massimo Russo
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Spinal, Natural history, Spinal Muscular Atrophies of Childhood, Outcome measures, Cohort Studies, Muscular Atrophy, Spinal, Upper Extremity, Neuromuscular disorders, Revised upper limb module, Spinal muscular atrophy, Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Internal medicine, medicine, Humans, Child, Child, Preschool, Disease Progression, Female, Longitudinal Studies, Middle Aged, Preschool, Genetics (clinical), business.industry, SMA, medicine.disease, Relative stability, Large cohort, Settore MED/26 - NEUROLOGIA, Muscular Atrophy, medicine.anatomical_structure, Neurology, Pediatrics, Perinatology and Child Health, Cardiology, Upper limb, Neurology (clinical), business, Real world data
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862b23e9e6b08e24fee4b1754d6d00fcTest
http://hdl.handle.net/10807/197786Test -
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المؤلفون: Carmelo Messina, Elena Passeri, G. Meola, Valeria A. Sansone, Luca Maria Sconfienza, Sabrina Corbetta
المصدر: Neuromuscular Disorders. 30:28-34
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Osteoporosis, Myotonic dystrophy, Body Mass Index, Fractures, Bone, 03 medical and health sciences, Absorptiometry, Photon, 0302 clinical medicine, Insulin resistance, Bone Density, Internal medicine, medicine, Humans, Myotonic Dystrophy, Testosterone, Mass index, Muscle, Skeletal, Pelvic Bones, Genetics (clinical), Bone mineral, business.industry, Skeletal muscle, Middle Aged, medicine.disease, Osteopenia, Bone Diseases, Metabolic, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, Neurology, Pediatrics, Perinatology and Child Health, Neurology (clinical), business, Body mass index, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f89558b3f08f80061fef61cb4c4dc0Test
https://doi.org/10.1016/j.nmd.2019.11.006Test -
3
المؤلفون: Jacqueline Montes, Marika Pane, Enrico Bertini, Francesco Muntoni, Maria Carmela Pera, Anna Lia Frongia, Amy Pasternak, Eugenio Mercuri, Valeria A. Sansone, John W. Day, Maria Sframeli, Francesca Salmin, Adele D'Amico, Matthew Civitello, Simona Lucibello, Sally Dunaway Young, Claudio Bruno, Laura Antonaci, Giorgia Coratti, Sara Carnicella, Tina Duong, Darryl C. De Vivo, Richard S. Finkel, Allan M. Glanzman, Sonia Messina, Paola Tacchetti, Basil T. Darras
مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Adolescent, Oligonucleotides, Spinal Muscular Atrophies of Childhood, Cohort Studies, Upper Extremity, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, 0302 clinical medicine, Internal medicine, Age related, Nusinersen, medicine, Functional outcome measures, Hammersmith Functional Motor Scale Expanded, Revised Upper Limb Module, Spinal Muscular Atrophy, Age Factors, Child, Child, Preschool, Female, Humans, Linear Models, Multivariate Analysis, Treatment effect, Preschool, Genetics (clinical), Settore MED/48 - SCIENZE INFERMIERISTICHE E TECNICHE NEURO-PSICHIATRICHE E RIABILITATIVE, business.industry, SMA, Spinal muscular atrophy type II, Natural history, 030104 developmental biology, medicine.anatomical_structure, Neurology, Pediatrics, Perinatology and Child Health, Cohort, Upper limb, Neurology (clinical), business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::506d0065b03b941235c643e5f4d33786Test
http://hdl.handle.net/11567/1087190Test -
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المؤلفون: Emilio Albamonte, Adele D'Amico, Sonia Messina, Valeria A. Sansone, Luca Mauro, Susanna Pozzi, Maria Carmela Pera, Marika Pane, Andrea Lizio, Enrico Bertini, Cristina Italiano, Claudio Bruno, Lucia Greco, Giorgia Coratti, Christine Zizzi, Alice Pirola, Maria Sframeli, Claudia Stancanelli, Chad Heatwole, Francesca Salmin, Jacopo Casiraghi, Eugenio Mercuri, Marina Pedemonte
مصطلحات موضوعية: 0301 basic medicine, Male, Severity of Illness Index, Internal validity, Cohort Studies, 0302 clinical medicine, Cost of Illness, Surveys and Questionnaires, Medicine, Child, Genetics (clinical), Settore MED/48 - SCIENZE INFERMIERISTICHE E TECNICHE NEURO-PSICHIATRICHE E RIABILITATIVE, Middle Aged, SMA, Muscular Atrophy, medicine.anatomical_structure, Test-retest reliability, Neurology, Italy, Cohort, Upper limb, Spinal muscular atrophy health index, Patient-reported outcome, Female, Adult, medicine.medical_specialty, Adolescent, Spinal, Muscular Atrophy, Spinal, 03 medical and health sciences, Patient-reported outcomes, Spinal muscular atrophy, Humans, Quality of Life, Reproducibility of Results, Translations, Patient Reported Outcome Measures, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Cronbach's alpha, Disease burden, business.industry, medicine.disease, 030104 developmental biology, Pediatrics, Perinatology and Child Health, Physical therapy, Neurology (clinical), business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f7d219115205388497280afb4c47d6aTest
http://hdl.handle.net/10807/182752Test -
5
المصدر: Neuromuscular Disorders. 24:365-367
مصطلحات موضوعية: musculoskeletal diseases, endocrine system, congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Myotonia Congenita, endocrine system diseases, Hormone Replacement Therapy, DNA Mutational Analysis, Muscle disorder, Asymptomatic, Diagnosis, Differential, Young Adult, Hypothyroidism, Channelopathy, Chloride Channels, Internal medicine, medicine, Humans, Genetics (clinical), CLCN1, biology, Myotonia congenita, business.industry, Skeletal muscle, medicine.disease, Myotonia, body regions, Thyroxine, Endocrinology, medicine.anatomical_structure, Neurology, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, Female, Neurology (clinical), medicine.symptom, Thyroid function, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63da7ef162127cb9a4549dc1d44ae08eTest
https://doi.org/10.1016/j.nmd.2014.01.006Test -
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المؤلفون: L. Colleoni, Massimiliano Filosto, Anna Ardissone, Tiziana Mongini, M. Lo Monaco, Sabrina Ravaglia, Giulia Ricci, Lorenzo Maggi, Gabriele Siciliano, Valeria A. Sansone, Antonella Pini, D. Kapetis, Pia Bernasconi, Renato Mantegazza, Isabella Moroni, Lucia Morandi, Elena Pegoraro, Liliana Vercelli, G. Meola, Raffaella Brugnoni
المصدر: Neuromuscular Disorders. 24:841-842
مصطلحات موضوعية: Genetics, CLCN1, Genetic heterogeneity, media_common.quotation_subject, Nonsense, Skeletal muscle, Periodic paralysis, Biology, Myotonia, medicine.disease, medicine.anatomical_structure, Neurology, Pediatrics, Perinatology and Child Health, medicine, biology.protein, Missense mutation, Neurology (clinical), Gene, Genetics (clinical), media_common
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::aa4bb10fc5cb83b0d214636597f04b93Test
https://doi.org/10.1016/j.nmd.2014.06.166Test -
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المؤلفون: Richard T. Moxley, Martin Schalling, Valeria A. Sansone, Qiu-Ping Yuan, Matt Krym, Donald Henderson, Maurice S. Swanson, Carl R. Urbinati, Ami Mankodi, Charles A. Thornton
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Mutant, Biology, Myotonic dystrophy, chemistry.chemical_compound, Ribonucleases, Trinucleotide Repeats, Genetics, medicine, Animals, Drosophila Proteins, Humans, Myotonic Dystrophy, MBNL1, Muscle, Skeletal, Molecular Biology, Gene, In Situ Hybridization, Fluorescence, Genetics (clinical), Aged, Cell Nucleus, Messenger RNA, Nuclear Proteins, RNA, General Medicine, Middle Aged, medicine.disease, Molecular biology, Cell nucleus, medicine.anatomical_structure, chemistry, Drosophila, Female, Trinucleotide repeat expansion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e736e609ea25f97a58381a65efa430d5Test
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034783271&partnerID=MN8TOARSTest