Mercuri E - Search Results

1

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study.

Mazzone E, Vasco G, Sormani MP, Torrente Y, Berardinelli A, Messina S, D'Amico A, Doglio L, Politano L, Cavallaro F, Frosini S, Bello L, Bonfiglio S, Zucchini E, De Sanctis R, Scutifero M, Bianco F, Rossi F, Motta MC, Sacco A, Donati MA, Mongini T, Pini A, Battini R, Pegoraro E, Pane M, Gasperini S, Previtali S, Napolitano S, Martinelli D, Bruno C, Vita G, Comi G, Bertini E, Mercuri E. Mazzone E, et al. Among authors: mercuri e. Neurology. 2011 Jul 19;77(3):250-6. doi: 10.1212/WNL.0b013e318225ab2e. Epub 2011 Jul 6. Neurology. 2011. PMID: 21734183

2

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.

Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Neuropediatrics. 1995 Feb;26(1):3-7. doi: 10.1055/s-2007-979711. Neuropediatrics. 1995. PMID: 7791947

3

Motor and perceptual-motor competence in children with Down syndrome: variation in performance with age.

Spanò M, Mercuri E, Randò T, Pantò T, Gagliano A, Henderson S, Guzzetta F. Spanò M, et al. Among authors: mercuri e. Eur J Paediatr Neurol. 1999;3(1):7-13. doi: 10.1053/ejpn.1999.0173. Eur J Paediatr Neurol. 1999. PMID: 10727186

4

Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy.

Dubowitz V, Kinali M, Main M, Mercuri E, Muntoni F. Dubowitz V, et al. Among authors: mercuri e. Eur J Paediatr Neurol. 2002;6(3):153-9. doi: 10.1053/ejpn.2002.0583. Eur J Paediatr Neurol. 2002. PMID: 12363102

5

Fracture prevalence in Duchenne muscular dystrophy.

McDonald DG, Kinali M, Gallagher AC, Mercuri E, Muntoni F, Roper H, Jardine P, Jones DH, Pike MG. McDonald DG, et al. Among authors: mercuri e. Dev Med Child Neurol. 2002 Oct;44(10):695-8. doi: 10.1017/s0012162201002778. Dev Med Child Neurol. 2002. PMID: 12418795 Free article.

6

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study.

Mercuri E, Messina S, Kinali M, Cini C, Longman C, Battini R, Cioni G, Muntoni F. Mercuri E, et al. Neuromuscul Disord. 2004 Feb;14(2):125-9. doi: 10.1016/j.nmd.2003.09.005. Neuromuscul Disord. 2004. PMID: 14733958

7

Pilot trial of phenylbutyrate in spinal muscular atrophy.

Mercuri E, Bertini E, Messina S, Pelliccioni M, D'Amico A, Colitto F, Mirabella M, Tiziano FD, Vitali T, Angelozzi C, Kinali M, Main M, Brahe C. Mercuri E, et al. Neuromuscul Disord. 2004 Feb;14(2):130-5. doi: 10.1016/j.nmd.2003.11.006. Neuromuscul Disord. 2004. PMID: 14733959 Clinical Trial.

8

Severe abnormalities of the pons in two infants with goldenhar syndrome.

Pane M, Baranello G, Battaglia D, Donvito V, Carnevale F, Stefanini MC, Guzzetta F, Mercuri E, Bertini E. Pane M, et al. Among authors: mercuri e. Neuropediatrics. 2004 Aug;35(4):234-8. doi: 10.1055/s-2004-820894. Neuropediatrics. 2004. PMID: 15328563

9

Prognostic value of EEG performed at term age in preterm infants.

Randò T, Ricci D, Luciano R, Frisone MF, Baranello G, Tonelli T, Pane M, Romagnoli C, Tortorolo G, Mercuri E, Guzzetta F. Randò T, et al. Among authors: mercuri e. Childs Nerv Syst. 2006 Mar;22(3):263-9. doi: 10.1007/s00381-005-1167-8. Epub 2005 Jun 1. Childs Nerv Syst. 2006. PMID: 15928967

10

Assessment of visual function in children with methylmalonic aciduria and homocystinuria.

Ricci D, Pane M, Deodato F, Vasco G, Randò T, Caviglia S, Dionisi-Vici C, Mercuri E. Ricci D, et al. Among authors: mercuri e. Neuropediatrics. 2005 Jun;36(3):181-5. doi: 10.1055/s-2005-865609. Neuropediatrics. 2005. PMID: 15944903

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