Showing results (271-280 of 346) with videos related to
Sort By:
Pageof 35
Neuromuscular Disorders : NMD|March 3, 2015
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian familyI Colombo, S Pagliarani, S Testolin, et al.Journal of the Neurological Sciences|April 24, 2012
Myotonia congenita: novel mutations in CLCN1 gene and functional characterizations in Italian patientsGianna Ulzi, Marzia Lecchi, Valeria Sansone, et al.Plos Genetics|March 29, 2014
An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selectionDiego Forni, Rachele Cagliani, Claudia Tresoldi, et al.Neurobiology of Aging|September 25, 2007
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutationAnna Bersano, Roberto Del Bo, Costanza Lamperti, et al.Molecular Biology and Evolution|February 8, 2013
Crohn's disease loci are common targets of protozoa-driven selectionRachele Cagliani, Uberto Pozzoli, Diego Forni, et al.Cell|September 1, 1976
Delta-beta-thalassemia is due to a gene deletionS Ottolenghi, P Comi, B Giglioni, et al.Frontiers in Neurology|July 5, 2022
Cognitive and Autonomic Dysfunction in Multiple System Atrophy Type P and C: A Comparative StudyGiulia Lazzeri, Giulia Franco, Teresa Difonzo, et al.Journal of Neuroimmunology|May 6, 2014
No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosisFranca R Guerini, Mario Clerici, Rachele Cagliani, et al.BMC Medical Genetics|March 15, 2011
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencingFrancesca Magri, Roberto Del Bo, Maria G D'Angelo, et al.Human Genetics|July 8, 2011
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysisRachele Cagliani, Matteo Fumagalli, Franca R Guerini, et al.Pageof 35