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Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant.
Mercuri E, Poppe M, Quinlivan R, Messina S, Kinali M, Demay L, Bourke J, Richard P, Sewry C, Pike M, Bonne G, Muntoni F, Bushby K. Mercuri E, et al. Among authors: messina s. Arch Neurol. 2004 May;61(5):690-4. doi: 10.1001/archneur.61.5.690. Arch Neurol. 2004. PMID: 15148145
Can clinical signs identify newborns with neuromuscular disorders?
Vasta I, Kinali M, Messina S, Guzzetta A, Kapellou O, Manzur A, Cowan F, Muntoni F, Mercuri E. Vasta I, et al. Among authors: messina s. J Pediatr. 2005 Jan;146(1):73-9. doi: 10.1016/j.jpeds.2004.08.047. J Pediatr. 2005. PMID: 15644826
Feeding problems and weight gain in Duchenne muscular dystrophy.
Pane M, Vasta I, Messina S, Sorleti D, Aloysius A, Sciarra F, Mangiola F, Kinali M, Ricci E, Mercuri E. Pane M, et al. Among authors: messina s. Eur J Paediatr Neurol. 2006 Sep-Nov;10(5-6):231-6. doi: 10.1016/j.ejpn.2006.08.008. Epub 2006 Oct 10. Eur J Paediatr Neurol. 2006. PMID: 17045498
Predictive factors for the development of scoliosis in Duchenne muscular dystrophy.
Kinali M, Main M, Eliahoo J, Messina S, Knight RK, Lehovsky J, Edge G, Mercuri E, Manzur AY, Muntoni F. Kinali M, et al. Among authors: messina s. Eur J Paediatr Neurol. 2007 May;11(3):160-6. doi: 10.1016/j.ejpn.2006.12.002. Epub 2007 Jan 25. Eur J Paediatr Neurol. 2007. PMID: 17257866 Clinical Trial.
432 results