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Archives of Disease in Childhood|February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centresA Vellodi, E P Young, A Cooper, et al.
Archives of Disease in Childhood|November 3, 1998
Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometryP T Clayton, M Doig, S Ghafari, et al.
Human Gene Therapy|October 6, 1998
Biodistribution and gene expression of lipid/plasmid complexes after systemic administrationR I Mahato, K Anwer, F Tagliaferri, et al.
Cancer Gene Therapy|September 7, 2000
Cationic lipid-based delivery system for systemic cancer gene therapyK Anwer, C Meaney, G Kao, et al.
Clinical and Experimental Immunology|August 24, 2004
Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiencyD Eastwood, K C Gilmour, K Nistala, et al.
The Journal of Hospital Infection|May 13, 2022
Repeated transmission of SARS-CoV-2 in an overcrowded Irish emergency department elucidated by whole-genome sequencingD Hare, C Meaney, J Powell, et al.
European Review for Medical and Pharmacological Sciences|February 26, 2020
Total cholesterol affects the outcome of patients with anterior cerebral artery-occluded acute ischemic stroke treated with thrombolysisL Niu, S-W Jiang, Y Wang, et al.
Dementia and Geriatric Cognitive Disorders Extra|September 11, 2012
Roles of Education and IQ in Cognitive Reserve in Parkinson's Disease-Mild Cognitive ImpairmentM J Armstrong, G Naglie, S Duff-Canning, et al.
Neurology|July 15, 2011
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriersC Marras, B Schüle, B Schuele, et al.
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