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Neuroradiology|January 7, 1999
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patientsL Farina, L Morandi, I Milanesi, et al.Journal of Neurology|September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic studyC Mariotti, G Uziel, F Carrara, et al.Journal of Neurology|September 1, 1993
Dystrophin abnormalities in Duchenne and Becker dystrophy carriers: correlation with cytoskeletal proteins and myosinsM Mora, L Morandi, A Piccinelli, et al.International Journal of Sports Medicine|November 24, 2001
Hemoglobin mass and peak oxygen uptake in untrained and trained residents of moderate altitudeD Böning, J Rojas, M Serrato, et al.Actas Urologicas Espanolas|September 1, 1994
[Transitional carcinomas of the urinary tract: synchronous and metachronous lesions]M Arrizabalaga, J Navarro, M Mora, et al.Communicable Disease Report. CDR Review|May 2, 1997
Outbreak of trichinosis in France associated with eating horse meatH Laurichesse, M Cambon, D Perre, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 22, 2008
GSK-3beta and alpha-catenin binding regions of beta-catenin exert opposing effects on the terminal ventral optic axonal projectionA Wiley, K Edalat, P Chiang, et al.Environmental Research|January 9, 2020
Early immune stimulation and childhood acute lymphoblastic leukemia in Costa Rica: A comparison of statistical approachesSophia Colombari Figueroa, Chris J Kennedy, Catharina Wesseling, et al.Advanced Drug Delivery Reviews|March 9, 2018
Tackling muscle fibrosis: From molecular mechanisms to next generation engineered models to predict drug deliveryS Bersini, M Gilardi, M Mora, et al.Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.Pageof 126