Muntoni F - Search Results

1

Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.

Janghra N, Morgan JE, Sewry CA, Wilson FX, Davies KE, Muntoni F, Tinsley J. Janghra N, et al. Among authors: muntoni f. PLoS One. 2016 Mar 14;11(3):e0150818. doi: 10.1371/journal.pone.0150818. eCollection 2016. PLoS One. 2016. PMID: 26974331 Free PMC article.

2

Muscle development genes: their relevance in neuromuscular disorders.

Muntoni F, Brown S, Sewry C, Patel K. Muntoni F, et al. Neuromuscul Disord. 2002 Jun;12(5):438-46. doi: 10.1016/s0960-8966(01)00326-1. Neuromuscul Disord. 2002. PMID: 12031617 Review.

3

The 3'-untranslated region of the dystrophin gene - conservation and consequences of loss.

Greener MJ, Sewry CA, Muntoni F, Roberts RG. Greener MJ, et al. Among authors: muntoni f. Eur J Hum Genet. 2002 Jul;10(7):413-20. doi: 10.1038/sj.ejhg.5200822. Eur J Hum Genet. 2002. PMID: 12107815

4

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.

5

Steroids in Duchenne muscular dystrophy: from clinical trials to genomic research.

Muntoni F, Fisher I, Morgan JE, Abraham D. Muntoni F, et al. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S162-5. doi: 10.1016/s0960-8966(02)00101-3. Neuromuscul Disord. 2002. PMID: 12206811

6

Muscle MRI findings in a three-generation family affected by Bethlem myopathy.

Mercuri E, Cini C, Counsell S, Allsop J, Zolkipli Z, Jungbluth H, Sewry C, Brown SC, Pepe G, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Eur J Paediatr Neurol. 2002;6(6):309-14. doi: 10.1016/s1090-3798(02)90618-5. Eur J Paediatr Neurol. 2002. PMID: 12401455

7

What's new in neuromuscular disorders? The congenital myopathies.

Jungbluth H, Sewry CA, Muntoni F. Jungbluth H, et al. Among authors: muntoni f. Eur J Paediatr Neurol. 2003;7(1):23-30. doi: 10.1016/s1090-3798(02)00136-8. Eur J Paediatr Neurol. 2003. PMID: 12615171 Review.

8

Phenotypic spectrum associated with mutations in the fukutin-related protein gene.

Mercuri E, Brockington M, Straub V, Quijano-Roy S, Yuva Y, Herrmann R, Brown SC, Torelli S, Dubowitz V, Blake DJ, Romero NB, Estournet B, Sewry CA, Guicheney P, Voit T, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Ann Neurol. 2003 Apr;53(4):537-42. doi: 10.1002/ana.10559. Ann Neurol. 2003. PMID: 12666124

9

Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.

Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, Dubowitz V. Nevo Y, et al. Among authors: muntoni f. Isr Med Assoc J. 2003 Feb;5(2):94-7. Isr Med Assoc J. 2003. PMID: 12674656 Free article.

10

Profound skeletal muscle depletion of alpha-dystroglycan in Walker-Warburg syndrome.

Jiménez-Mallebrera C, Torelli S, Brown SC, Feng L, Brockington M, Sewry CA, Beltrán-Valero De Bernabé D, Muntoni F. Jiménez-Mallebrera C, et al. Among authors: muntoni f. Eur J Paediatr Neurol. 2003;7(3):129-37. doi: 10.1016/s1090-3798(03)00042-4. Eur J Paediatr Neurol. 2003. PMID: 12788039

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