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European Journal of Neurology|June 17, 2010
Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegiaR Battini, A Fogli, D Borghetti, et al.American Journal of Human Genetics|September 14, 2001
Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humansC B Item, S Stöckler-Ipsiroglu, C Stromberger, et al.Neuropediatrics|March 6, 2004
Brain lactic alkalosis in Aicardi-Goutières syndromeN J Robertson, P Stafler, R Battini, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|May 18, 1999
Visual function in term infants with hypoxic-ischaemic insults: correlation with neurodevelopment at 2 years of ageE Mercuri, L Haataja, A Guzzetta, et al.Recenti Progressi in Medicina|December 1, 1996
[The use of echo-guided fine-needle biopsy in the diagnosis of nodular hepatic lesions]G Cioni, A Ferrari, P D'Alimonte, et al.AAPS Pharmscitech|January 20, 2004
Factorial analysis of the influence of dissolution medium on drug release from carrageenan-diltiazem complexesM C Bonferoni, S Rossi, F Ferrari, et al.Developmental Cognitive Neuroscience|February 3, 2022
Detection and analysis of cortical beta bursts in developmental EEG dataHolly Rayson, Ranjan Debnath, Sanaz Alavizadeh, et al.Annals of Human Biology|December 28, 1999
Anthropometry fails in classifying bone mineral status in postmenopausal womenG Bedogni, G Simonini, S Viaggi, et al.Cardiologia (Rome, Italy)|March 1, 1995
[Identification of multivessel coronary disease using myocardial Thallium-201 and dipyridamole scintigraphy in acute myocardial infarction in the thrombolytic era]B Palagi, J Heyman, A Belloni, et al.Biochemical and Biophysical Research Communications|May 14, 1993
Progesterone induced expression of alkaline phosphatase is associated with a secretory phenotype in T47D breast cancer cellsD Di Lorenzo, M Giannì, G F Savoldi, et al.Pageof 85