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Der Nervenarzt|October 3, 1998
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]G Kuhlenbäumer, M Bocchicchio, W Kress, et al.Cytogenetics and Cell Genetics|February 15, 2001
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses)W Kress, H Collmann, M Büsse, et al.Klinische Padiatrie|May 3, 2012
Duchenne muscular dystrophy in a 4-year-old girl due to heterozygous frame shift deletion of the dystrophin gene and skewed X-inactivationA Schänzer, I Rau, W Kress, et al.BMC Research Notes|December 5, 2013
The coding region of the UFGT gene is a source of diagnostic SNP markers that allow single-locus DNA genotyping for the assessment of cultivar identity and ancestry in grapevine (Vitis vinifera L.)Silvia Nicolè, Gianni Barcaccia, David L Erickson, et al.Annals of Neurology|November 1, 1995
Monocyte/macrophage differentiation in early multiple sclerosis lesionsW Brück, P Porada, S Poser, et al.Acta Neurologica Scandinavica|September 1, 1995
Specificity of intrathecal IgG synthesis for HTLV-1 core and envelope proteins in HAM/TSPB Kitze, M Puccioni-Sohler, J Schäffner, et al.European Journal of Neurology|April 5, 2005
Whipple's disease presenting as an isolated lesion of the cervical spinal cordA Schröter, J Brinkhoff, T Günthner-Lengsfeld, et al.Neurology|November 1, 1993
Soluble ICAM-1 serum levels in multiple sclerosis and viral encephalitisH P Hartung, M Michels, K Reiners, et al.Neurology|September 25, 2003
Fatigue in MS is related to sympathetic vasomotor dysfunctionP Flachenecker, A Rufer, I Bihler, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Progressive sudomotor dysfunction in amyotrophic lateral sclerosisM Beck, R Giess, T Magnus, et al.Pageof 288