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American Journal of Diseases of Children (1960)|December 1, 1993
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysisV Schuster, W Kress, W Friedrich, et al.
Archives of Dermatology|April 1, 1998
Focal hyperhidrosis: effective treatment with intracutaneous botulinum toxinM Naumann, U Hofmann, I Bergmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 1998
Imaging the pre- and postsynaptic side of striatal dopaminergic synapses in idiopathic cervical dystonia: a SPECT study using [123I] epidepride and [123I] beta-CITM Naumann, W Pirker, K Reiners, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.
The British Journal of Ophthalmology|May 26, 1999
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase geneU Felbor, Y Mutsch, F Grehn, et al.
American Journal of Medical Genetics|April 29, 1998
Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3B Petersen, H M Strassburg, W Feichtinger, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|December 4, 2002
Atrophic dermatofibroma: a case report and review of the literatureAli Hendi, Drazen M Jukic, Douglas W Kress, et al.
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