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Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 8, 2013
Diagnostic measures for sarcopenia and bone mineral densityA Y Bijlsma, M C G Meskers, M Molendijk, et al.
Age (Dordrecht, Netherlands)|July 3, 2013
Diagnostic criteria for sarcopenia and physical performanceA Y Bijlsma, C G M Meskers, N van den Eshof, et al.
Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Neuromuscular Disorders : NMD|February 5, 2014
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patientsE Mazzone, R De Sanctis, L Fanelli, et al.
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