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JIMD Reports|February 28, 2016
Clinical Evolution After Enzyme Replacement Therapy in Twins with the Severe Form of Maroteaux-Lamy SyndromeM Pineda, M O'Callaghan, A Fernandez Lopez, et al.
International Journal of Cosmetic Science|May 22, 2009
Applications of ternary systems in specific cosmetic formulationsF Comelles, V Megias, J Sánchez, et al.
Investigative Ophthalmology & Visual Science|April 29, 2008
VIP and VIP gene silencing modulation of differentiation marker N-cadherin and cell shape of corneal endothelium in human corneas ex vivoShay-Whey M Koh, Krish Chandrasekara, Cara J Abbondandolo, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|December 1, 1996
The 5' part of the human H19 RNA contains cis-acting elements hampering its translatabilityA Joubel, J J Curgy, H Pelczar, et al.
Revista De Neurologia|October 21, 1999
[Diagnostic strategy for mitochondrial diseases]A Galán-Ortega, J Coll-Cantí, A Padrós-Fluvià, et al.
American Journal of Medical Genetics|May 9, 2001
Mutation and haplotype analyses in 26 Spanish Sanfilippo syndrome type A patients: possible single origin for 1091delC mutationA Chabás, M Montfort, M Martínez-Campos, et al.
Journal of Autoimmunity|August 11, 1999
Th1 predominance and perforin expression in minor salivary glands from patients with primary Sjögren's syndromeE C Kolkowski, P Reth, F Pelusa, et al.
Human Mutation|September 23, 1998
Mutation 1091delC is highly prevalent in Spanish Sanfilippo syndrome type A patientsM Montfort, L Vilageliu, N Garcia-Giralt, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 1, 1996
Increased radionuclide uptake on bone scintiscans: a common but not clinically significant finding for human immunodeficiency virus type 1-infected patients free of osteoarticular symptomsJ Rubiés-Prat, J Coll, L del Río, et al.
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