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Medicina Intensiva|April 30, 2021
Mathematical model optimized for prediction and health care planning for COVID-19J M Garrido, D Martínez-Rodríguez, F Rodríguez-Serrano, et al.
Neuromuscular Disorders : NMD|June 18, 2005
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genesA D'Amico, G Haliloglu, P Richard, et al.
Endocrine Pathology|January 1, 1995
Immunohistochemical Analysis of the Cell Cycle-Associated Antigens Ki-67 and Retinoblastoma Protein in Parathyroid Carcinomas and AdenomasRicardo V. Lloyd, J. Aidan Carney, Jorge A. Ferreiro, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Mutation Research|June 12, 1996
Somatic recombination, gene amplification and cancerC Ramel, H Cederberg, J Magnusson, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, et al.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Neurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.
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