Main M - Search Results

1

Longitudinal changes in respiratory and upper limb function in a pediatric type III spinal muscular atrophy cohort after loss of ambulation.

Wolfe A, Scoto M, Milev E, Muni Lofra R, Abbott L, Wake R, Rohwer A, Main M, Baranello G, Mayhew A, Marini-Bettolo C, Muntoni F. Wolfe A, et al. Among authors: main m. Muscle Nerve. 2021 Nov;64(5):545-551. doi: 10.1002/mus.27404. Epub 2021 Sep 4. Muscle Nerve. 2021. PMID: 34432301

2

An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy.

Kinali M, Mercuri E, Main M, Muntoni F, Dubowitz V. Kinali M, et al. Among authors: main m. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S169-74. doi: 10.1016/s0960-8966(02)00097-4. Neuromuscul Disord. 2002. PMID: 12206813 Clinical Trial.

3

The Hammersmith functional motor scale for children with spinal muscular atrophy: a scale to test ability and monitor progress in children with limited ambulation.

Main M, Kairon H, Mercuri E, Muntoni F. Main M, et al. Eur J Paediatr Neurol. 2003;7(4):155-9. doi: 10.1016/s1090-3798(03)00060-6. Eur J Paediatr Neurol. 2003. PMID: 12865054

4

Serial casting of the ankles in Duchenne muscular dystrophy: can it be an alternative to surgery?

Main M, Mercuri E, Haliloglu G, Baker R, Kinali M, Muntoni F. Main M, et al. Neuromuscul Disord. 2007 Mar;17(3):227-30. doi: 10.1016/j.nmd.2006.12.002. Epub 2007 Feb 15. Neuromuscul Disord. 2007. PMID: 17303425 Clinical Trial.

5

Daily salbutamol in young patients with SMA type II.

Pane M, Staccioli S, Messina S, D'Amico A, Pelliccioni M, Mazzone ES, Cuttini M, Alfieri P, Battini R, Main M, Muntoni F, Bertini E, Villanova M, Mercuri E. Pane M, et al. Among authors: main m. Neuromuscul Disord. 2008 Jul;18(7):536-40. doi: 10.1016/j.nmd.2008.05.004. Epub 2008 Jun 24. Neuromuscul Disord. 2008. PMID: 18579379 Clinical Trial.

6

Is there post-natal muscle growth in amyoplasia? A sequential MRI study.

Mercuri E, Manzur A, Main M, Alsopp J, Muntoni F. Mercuri E, et al. Among authors: main m. Neuromuscul Disord. 2009 Jun;19(6):444-5. doi: 10.1016/j.nmd.2009.03.006. Epub 2009 May 27. Neuromuscul Disord. 2009. PMID: 19477646 No abstract available.

7

Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trials.

Arechavala-Gomeza V, Kinali M, Feng L, Guglieri M, Edge G, Main M, Hunt D, Lehovsky J, Straub V, Bushby K, Sewry CA, Morgan JE, Muntoni F. Arechavala-Gomeza V, et al. Among authors: main m. Neuromuscul Disord. 2010 May;20(5):295-301. doi: 10.1016/j.nmd.2010.03.007. Epub 2010 Apr 14. Neuromuscul Disord. 2010. PMID: 20395141 Free article.

8

Assessing upper limb function in nonambulant SMA patients: development of a new module.

Mazzone E, Bianco F, Martinelli D, Glanzman AM, Messina S, De Sanctis R, Main M, Eagle M, Florence J, Krosschell K, Vasco G, Pelliccioni M, Lombardo M, Pane M, Finkel R, Muntoni F, Bertini E, Mercuri E. Mazzone E, et al. Among authors: main m. Neuromuscul Disord. 2011 Jun;21(6):406-12. doi: 10.1016/j.nmd.2011.02.014. Epub 2011 Mar 21. Neuromuscul Disord. 2011. PMID: 21421316

9

Development of a functional assessment scale for ambulatory boys with Duchenne muscular dystrophy.

Scott E, Eagle M, Mayhew A, Freeman J, Main M, Sheehan J, Manzur A, Muntoni F; North Star Clinical Network for Paediatric Neuromuscular Disease. Scott E, et al. Among authors: main m. Physiother Res Int. 2012 Jun;17(2):101-9. doi: 10.1002/pri.520. Epub 2011 Sep 23. Physiother Res Int. 2012. PMID: 21954141

10

Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations.

Burke G, Hiscock A, Klein A, Niks EH, Main M, Manzur AY, Ng J, de Vile C, Muntoni F, Beeson D, Robb S. Burke G, et al. Among authors: main m. Neuromuscul Disord. 2013 Feb;23(2):170-5. doi: 10.1016/j.nmd.2012.11.004. Epub 2012 Dec 5. Neuromuscul Disord. 2013. PMID: 23219351 Free article.

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