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Neuropediatrics|May 1, 1990
Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndromeN Illum, K Taudorf, C Heilmann, et al.Journal of Dental Research|July 5, 2002
Expression of N-acetyltransferases in periodontal granulation tissueP Meisel, J Giebel, M Peters, et al.Allergy|August 11, 2017
Hereditary angioedema with a mutation in the plasminogen geneK Bork, K Wulff, L Steinmüller-Magin, et al.Anaesthesia|August 23, 2016
Sleep disturbance in patients taking opioid medication for chronic back painJ A Robertson, R J Purple, P Cole, et al.Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|August 15, 1988
[Initial results of genetic carrier diagnosis in risk pedigrees with hemophilia A and B in East Germany]M Wehnert, F H Herrmann, H Metzke, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2006
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 geneF H Herrmann, G Auerswald, A Ruiz-Saez, et al.Disease Markers|April 1, 1997
Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysisK Wulff, U Ebener, C S Wehnert, et al.Journal of Medical Genetics|November 1, 1990
Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and HungaryA Speer, U Kräft, R Hanke, et al.Neuromuscular Disorders : NMD|June 26, 1999
Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophyM Hoeltzenbein, T Karow, J A Zeller, et al.British Journal of Haematology|April 12, 2001
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic dataV Ivaskevicius, R Jurgutis, S Rost, et al.Pageof 11