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European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.Cancer Genetics and Cytogenetics|July 15, 1994
Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterationsI Magnani, S Guerneri, B Pollo, et al.Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.American Journal of Human Genetics|June 1, 1996
Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10qR Albarosa, B M Colombo, L Roz, et al.Human Gene Therapy|July 20, 1997
Limited efficacy of the HSV-TK/GCV system for gene therapy of malignant gliomas and perspectives for the combined transduction of the interleukin-4 geneS Benedetti, F Dimeco, B Pollo, et al.Neurobiology of Disease|May 22, 2007
Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stagesK Varani, A-C Bachoud-Lévi, C Mariotti, et al.Pageof 5