المؤلفون: Brigitte, Mueller, Raoul, Engelbert, Frances, Baratta-Ziska, Bart, Bartels, Nicole, Blanc, Evelise, Brizola, Paolo, Fraschini, Claire, Hill, Caroline, Marr, Lisa, Mills, Kathleen, Montpetit, Verity, Pacey, Miguel, Rodriguez Molina, Marleen, Schuuring, Chantal, Verhille, Olga, de Vries, Eric, Hiu Kwong Yeung, Oliver, Semler, Hogeschool van Amsterdam, Lectoraat Fysiotherapie - Transitie van Zorg bij Complexe Patiënten

المصدر: 13(158)

URL الوصول: https://pure.hva.nl/ws/files/5225099/engelbert_202018_202.pdf
https://research.hva.nl/en/publications/7f00d584-1cca-43ab-8996-69a865f2390b

الاتاحة: http://www.hbo-kennisbank.nl/en/page/hborecord.view/?uploadId=amsterdam_pure:oai:pure.hva.nl:publications/7f00d584-1cca-43ab-8996-69a865f2390b

المؤلفون: Brigitte Mueller, Raoul Engelbert, Frances Baratta-Ziska, Bart Bartels, Nicole Blanc, Evelise Brizola, Paolo Fraschini, Claire Hill, Caroline Marr, Lisa Mills, Kathleen Montpetit, Verity Pacey, Miguel Rodriguez Molina, Marleen Schuuring, Chantal Verhille, Olga de Vries, Eric Hiu Kwong Yeung, Oliver Semler

المصدر: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)

مصطلحات موضوعية: Osteogenesis imperfecta, Physiotherapy, Occupational therapy, Mobility, Rehabilitation, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13023-018-0905-4; https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/63a7f964372f474a8efedc7d4512fc2c

المؤلفون: Verity Pacey, Brigitte Mueller, Eric Hiu Kwong Yeung, Frances Baratta-Ziska, Nicole Blanc, Chantal Verhille, Bart Bartels, Miguel Rodriguez Molina, Kathleen Montpetit, Claire Hill, Paolo Fraschini, Olga de Vries, Caroline Marr, Evelise Brizola, Oliver Semler, Marleen Schuuring, Lisa Mills, Raoul H.H. Engelbert

المساهمون: Hogeschool van Amsterdam, Lectoraat Fysiotherapie - Transitie van Zorg bij Complexe Patiënten, APH - Aging & Later Life, Rehabilitation medicine, AMS - Restoration & Development, ANS - Neuroinfection & -inflammation

المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 13(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Orphanet Journal of Rare Diseases, 13(158)
Orphanet journal of rare diseases, 13:158. BioMed Central

مصطلحات موضوعية: Statement (logic), medicine.medical_treatment, CHILDHOOD, lcsh:Medicine, Research & Experimental Medicine, MUSCLE STRENGTH, 0302 clinical medicine, Surveys and Questionnaires, Pharmacology (medical), Position Statement, Child, Physiotherapy, Genetics (clinical), GENOTYPE-PHENOTYPE CORRELATIONS, Genetics & Heredity, Mobility, Rehabilitation, General Medicine, Osteogenesis Imperfecta, IMPAIRMENT, SPONDYLODESIS, Medicine, Research & Experimental, Osteogenesis imperfecta, Child, Preschool, BONE, Life Sciences & Biomedicine, Occupational therapy, musculoskeletal diseases, medicine.medical_specialty, Adolescent, Pharmacology toxicology, education, 030209 endocrinology & metabolism, 03 medical and health sciences, Occupational Therapists, medicine, Humans, In patient, SCOLIOSIS, Science & Technology, business.industry, DISABILITY, lcsh:R, medicine.disease, PERCEIVED COMPETENCE, Physical Therapists, Physical therapy, Quality of Life, Personal experience, business, FOLLOW-UP, 030217 neurology & neurosurgery

وصف الملف: Electronic; image/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55091e651f15df6a9a7540dc8cec6703
https://lirias.kuleuven.be/handle/20.500.12942/703532

المؤلفون: Duygu Selcen, Sandra Meulemans, Luc Régal, John W.M. Creemers, Chantal Verhille, Andrew G. Engel, Xin Ming Shen

المصدر: Neurology. 82:1254-1260

مصطلحات موضوعية: Proband, medicine.medical_specialty, Nonsense mutation, Neuromuscular transmission, Biology, Article, Growth hormone deficiency, Internal medicine, medicine, Humans, Muscle, Skeletal, Myasthenic Syndromes, Congenital, Cystinuria, Muscle Weakness, Serine Endopeptidases, Infant, Muscle weakness, Congenital myasthenic syndrome, medicine.disease, Phenotype, Endocrinology, Pyridostigmine, Chromosomes, Human, Pair 2, Female, Neurology (clinical), medicine.symptom, Prolyl Oligopeptidases, Gene Deletion, medicine.drug

وصف الملف: Print-Electronic; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb20c8b6466363fc844e9d0446e9e9f
https://doi.org/10.1212/wnl.0000000000000295