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Nature|July 11, 2008
Structure of the Ebola virus glycoprotein bound to an antibody from a human survivorJeffrey E Lee, Marnie L Fusco, Ann J Hessell, et al.
Archives of General Psychiatry|February 1, 1979
Psychotherapy in the goldfish bowl: the role of the indigenous therapistJ F Borus, M Anastasi, R Casoni, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2001
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VIO Camacho Vanegas, E Bertini, R Z Zhang, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
European Journal of Clinical Investigation|December 12, 2001
Glutathione in blood of patients with Friedreich's ataxiaF Piemonte, A Pastore, G Tozzi, et al.
Clinical Genetics|January 15, 2008
Genotype-phenotype correlation in five Pelizaeus-Merzbacher disease patients with PLP1 gene duplicationsS Regis, R Biancheri, E Bertini, et al.
Neuromuscular Disorders : NMD|July 10, 1999
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagenG Pepe, E Bertini, B Giusti, et al.
European Review for Medical and Pharmacological Sciences|June 19, 2010
Elasticity/distensibility of the ascending aorta: basal conditions and simulated conditions from space flightsN Alessandri, F Tufano, M Petrassi, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 23, 2023
Recombinant Soluble Henipavirus Glycoprotein PreparationLianying Yan, Spencer L Sterling, Deborah L Fusco, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
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