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Journal of the Neurological Sciences|July 30, 1999
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patientsM Gomez-Lira, C Perusi, M Mottes, et al.Human Genetics|October 1, 1995
A common beta hexosaminidase gene mutation in adult Sandhoff disease patientsM Gomez-Lira, A Sangalli, M Mottes, et al.Human Molecular Genetics|December 1, 1994
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helixA Forlino, F Zolezzi, M Valli, et al.Bone Marrow Transplantation|January 1, 1991
An assessment of chimeric transcript detection in CML patients after bone marrow transplantationG Martinelli, M Sessarego, P Gasparini, et al.Journal of Hypertension|June 8, 2001
Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery diseaseO Olivieri, C Stranieri, D Girelli, et al.Oncology|January 1, 1996
Vinorelbine and mitomycin C in anthracycline-pretreated patients with advanced breast cancerP Vici, L Di Lauro, S Carpano, et al.Journal of Medical Genetics|August 27, 1998
Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian populationE Trabetti, V Cusin, G Malerba, et al.ESMO Open|December 10, 2024
Uncertainties about the benefit-risk balance of oncology medicines assessed by the European Medicines AgencyA C Taams, C A Herberts, A C G Egberts, et al.Journal of Neuroimmunology|November 26, 2002
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosisM Gomez-Lira, G Moretto, D Bonamini, et al.Respiratory Medicine|October 30, 1999
alpha 1-antitrypsin TAQ I polymorphism and alpha 1-antichymotrypsin mutations in patients with obstructive pulmonary diseaseM G Benetazzo, L S Gilè, C Bombieri, et al.Pageof 15