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1
المساهمون: Revalidatiegeneeskunde, RS: CAPHRI School for Public Health and Primary Care
المصدر: Spinal Cord, 51, 739-44
Spinal Cord, 51(10), 739-744. Nature Publishing Group
Spinal Cord, 51, 10, pp. 739-44مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, medicine.medical_treatment, Statistics as Topic, Patient subgroups, tetraplegia, Quadriplegia, Disability Evaluation, Young Adult, Physical medicine and rehabilitation, Activities of Daily Living, medicine, upper extremity, Humans, hand function test, Tetraplegia, Scale type, Spinal Cord Injuries, Level measurement, Aged, Rehabilitation, Rasch model, Hand function, Rasch analysis, General Medicine, Middle Aged, medicine.disease, Hand, Mitochondrial medicine [IGMD 8], Cross-Sectional Studies, Neurology, Physical therapy, Female, Neurology (clinical), Completeness (statistics), Psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfd1c83db10567a92737d91ee3d45ef1Test
https://doi.org/10.1038/sc.2013.54Test -
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المؤلفون: Henk A.M. Seelen, Rob J. E. M. Smeets, Annemie Spooren, G.J. Snoek, C. Arnould
المساهمون: Revalidatiegeneeskunde, RS: CAPHRI School for Public Health and Primary Care
المصدر: Spinal Cord, 51, 10, pp. 745-9
Spinal Cord, 51, 745-9
Spinal Cord, 51(10), 745-749. Nature Publishing Groupمصطلحات موضوعية: Adult, Male, medicine.medical_specialty, medicine.medical_treatment, motor skill, Quadriplegia, Cohort Studies, Physical medicine and rehabilitation, test, medicine, upper extremity, Humans, Longitudinal Studies, Longitudinal cohort, Tetraplegia, Spinal Cord Injuries, Aged, Hand function, Rehabilitation, Rasch model, business.industry, General Medicine, Middle Aged, reference values, Interval Scale, medicine.disease, spinal cord injury, Test (assessment), Mitochondrial medicine [IGMD 8], Neurology, Reference values, Physical therapy, Female, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86c58352c387e213fe07f87a124cafaTest
https://doi.org/10.1038/sc.2013.73Test -
3
المؤلفون: J. van Reeuwijk, L. De Meirleir, J Ranells, G Gillessen Kaesbach, Maciej Adamowicz, Emmanuelle Lemyre, I Salafsky, Jolanta Sykut-Cegielska, Eva Morava, Han G. Brunner, Peter Meinecke, Zsolt Urban, Ron A. Wevers, Dirk J. Lefeber
المساهمون: Pediatrics
المصدر: European Journal of Human Genetics, 16, 1, pp. 28-35
European Journal of Human Genetics, 16, 28-35مصطلحات موضوعية: Male, Systemic disease, medicine.medical_specialty, Pathology, cutis laxa syndrome, Glycosylation, Energy and redox metabolism [NCMLS 4], Genetics and epigenetic pathways of disease [NCMLS 6], Hearing loss, Central nervous system, Genes, Recessive, Biology, Neuroinformatics [DCN 3], Cutis Laxa, Genomic disorders and inherited multi-system disorders [IGMD 3], Internal medicine, Genetics, medicine, Perception and Action [DCN 1], Humans, Abnormalities, Multiple, isoelectric focusing, Child, Genetics (clinical), Genetic heterogeneity, Infant, Syndrome, Glycostation disorders [IGMD 4], medicine.disease, Phenotype, Neuromuscular development and genetic disorders [UMCN 3.1], Pedigree, Endocrinology, medicine.anatomical_structure, Palpebral fissure, Mitochondrial medicine [IGMD 8], Genetic defects of metabolism [UMCN 5.1], Child, Preschool, Female, glycosylation defect, medicine.symptom, Congenital disorder of glycosylation, Metabolism, Inborn Errors, Cutis laxa, Immunity, infection and tissue repair [NCMLS 1]
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f54df43fb286e2c958ad3929c16252d9Test
https://hdl.handle.net/20.500.14017/77a97e3e-58b3-4672-8827-9b29485f396eTest
