Showing results (181-190 of 246) with videos related to
Sort By:
Pageof 25
Cartilage|November 4, 2017
Imaging of Folate Receptor Expressing Macrophages in the Rat Groove Model of Osteoarthritis: Using a New DOTA-Folate ConjugateHuub M de Visser, Nicoline M Korthagen, Cristina Müller, et al.Journal of Neurology|May 20, 2008
Interpretation of electrodiagnostic findings in sporadic progressive muscular atrophyJ Visser, M de Visser, R M Van den Berg-Vos, et al.Neuromuscular Disorders : NMD|July 1, 1993
Linkage and apparent heterogeneity in proximal spinal muscular atrophiesJ M Cobben, H Scheffer, M De Visser, et al.Journal of Medical Genetics|March 1, 1994
Apparent SMA I unlinked to 5qJ M Cobben, H Scheffer, M de Visser, et al.Human Genetics|December 1, 1991
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2J E Hoogendijk, G W Hensels, I Zorn, et al.Clinical Neurology and Neurosurgery|May 22, 2021
Distal muscle weakness and optic atrophy without central nervous system involvement in a patient with a homozygous missense mutation in the C19ORF12-geneR J de Vries, B Jaeger, D M E I Hellebrekers, et al.Nederlands Tijdschrift Voor Geneeskunde|October 6, 2005
[The practice guideline 'Dermatomyositis, polymyositis and sporadic inclusion body myositis']J E Hoogendijk, J W J Bijlsma, B G M van Engelen, et al.BMC Pregnancy and Childbirth|February 10, 2018
Development of a tailored strategy to improve postpartum hemorrhage guideline adherenceSuzan M de Visser, Mallory D Woiski, Richard P Grol, et al.Plos Genetics|March 17, 2011
Initial mutations direct alternative pathways of protein evolutionMerijn L M Salverda, Eynat Dellus, Florien A Gorter, et al.Journal of the Neurological Sciences|May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspectsG J Jöbsis, E S Louwerse, M de Visser, et al.Pageof 25