Muntoni F - Search Results

1

The Clinical Development of Taldefgrobep Alfa: An Anti-Myostatin Adnectin for the Treatment of Duchenne Muscular Dystrophy.

Muntoni F, Byrne BJ, McMillan HJ, Ryan MM, Wong BL, Dukart J, Bansal A, Cosson V, Dreghici R, Guridi M, Rabbia M, Staunton H, Tirucherai GS, Yen K, Yuan X, Wagner KR; Taldefgrobep Alfa Study Group. Muntoni F, et al. Neurol Ther. 2024 Feb;13(1):183-219. doi: 10.1007/s40120-023-00570-w. Epub 2024 Jan 8. Neurol Ther. 2024. PMID: 38190001 Free PMC article.

2

Congenital muscular dystrophies.

Mercuri E, Sewry C, Brown SC, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Semin Pediatr Neurol. 2002 Jun;9(2):120-31. doi: 10.1053/spen.2002.33802. Semin Pediatr Neurol. 2002. PMID: 12138996 Review.

3

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: muntoni f. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S169-74. doi: 10.1016/s0960-8966(02)00097-4. Neuromuscul Disord. 2002. PMID: 12206813 Clinical Trial.

4

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: muntoni f. Dev Med Child Neurol. 2002 Oct;44(10):695-8. doi: 10.1017/s0012162201002778. Dev Med Child Neurol. 2002. PMID: 12418795 Free article.

5

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. Among authors: muntoni f. Eur J Paediatr Neurol. 2003;7(4):155-9. doi: 10.1016/s1090-3798(03)00060-6. Eur J Paediatr Neurol. 2003. PMID: 12865054

6

Antenatal and postnatal brain magnetic resonance imaging in muscle-eye-brain disease.

Longman C, Mercuri E, Cowan F, Allsop J, Brockington M, Jimenez-Mallebrera C, Kumar S, Rutherford M, Toda T, Muntoni F. Longman C, et al. Among authors: muntoni f. Arch Neurol. 2004 Aug;61(8):1301-6. doi: 10.1001/archneur.61.8.1301. Arch Neurol. 2004. PMID: 15313851

7

Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders.

Mercuri E, Jungbluth H, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Curr Opin Neurol. 2005 Oct;18(5):526-37. doi: 10.1097/01.wco.0000183947.01362.fe. Curr Opin Neurol. 2005. PMID: 16155435 Review.

8

Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations.

Mercuri E, Topaloglu H, Brockington M, Berardinelli A, Pichiecchio A, Santorelli F, Rutherford M, Talim B, Ricci E, Voit T, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Arch Neurol. 2006 Feb;63(2):251-7. doi: 10.1001/archneur.63.2.251. Arch Neurol. 2006. PMID: 16476814

9

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. Among authors: muntoni f. 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.

10

Differential diagnosis of congenital muscular dystrophies.

Klein A, Clement E, Mercuri E, Muntoni F. Klein A, et al. Among authors: muntoni f. Eur J Paediatr Neurol. 2008 Sep;12(5):371-7. doi: 10.1016/j.ejpn.2007.10.002. Epub 2007 Dec 3. Eur J Paediatr Neurol. 2008. PMID: 18588847

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