Muntoni F - Search Results

1

Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy.

Crilley JG, Boehm EA, Rajagopalan B, Blamire AM, Styles P, Muntoni F, Hilton-Jones D, Clarke K. Crilley JG, et al. Among authors: muntoni f. J Am Coll Cardiol. 2000 Nov 15;36(6):1953-8. doi: 10.1016/s0735-1097(00)00960-8. J Am Coll Cardiol. 2000. PMID: 11092670 Free article.

2

Correlative MR imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy.

Lodi R, Muntoni F, Taylor J, Kumar S, Sewry CA, Blamire A, Styles P, Taylor DJ. Lodi R, et al. Among authors: muntoni f. Neuromuscul Disord. 1997 Dec;7(8):505-11. doi: 10.1016/s0960-8966(97)00108-9. Neuromuscul Disord. 1997. PMID: 9447608

3

Reduced cytosolic acidification during exercise suggests defective glycolytic activity in skeletal muscle of patients with Becker muscular dystrophy. An in vivo 31P magnetic resonance spectroscopy study.

Lodi R, Kemp GJ, Muntoni F, Thompson CH, Rae C, Taylor J, Styles P, Taylor DJ. Lodi R, et al. Among authors: muntoni f. Brain. 1999 Jan;122 ( Pt 1):121-30. doi: 10.1093/brain/122.1.121. Brain. 1999. PMID: 10050900

4

Congenital muscular dystrophy with short stature, proximal contractures and distal laxity.

Mercuri E, Lampe A, Straub V, Yuva Y, Longman C, Wright M, Brown S, Sewry C, Bonnemann C, Kinali M, Brockington M, Hausser I, Hilton Jones D, Voit T, Bushby K, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Neuropediatrics. 2004 Aug;35(4):224-9. doi: 10.1055/s-2004-821084. Neuropediatrics. 2004. PMID: 15328561

5

Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy.

Spyrou N, Philpot J, Foale R, Camici PG, Muntoni F. Spyrou N, et al. Among authors: muntoni f. Am Heart J. 1998 Sep;136(3):474-6. doi: 10.1016/s0002-8703(98)70222-4. Am Heart J. 1998. PMID: 9736139

6

Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy.

Mercuri E, Anker S, Philpot J, Sewry C, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Pediatr Neurol. 1998 May;18(5):399-401. doi: 10.1016/s0887-8994(97)00222-1. Pediatr Neurol. 1998. PMID: 9650678

7

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.

Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, Muntoni F. Philpot J, et al. Among authors: muntoni f. Neuromuscul Disord. 1999 Mar;9(2):81-5. doi: 10.1016/s0960-8966(98)00110-2. Neuromuscul Disord. 1999. PMID: 10220862 Clinical Trial.

8

Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.

Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Neuropediatrics. 2002 Feb;33(1):10-4. doi: 10.1055/s-2002-23593. Neuropediatrics. 2002. PMID: 11930270

9

Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.

Mestroni L, Rocco C, Gregori D, Sinagra G, Di Lenarda A, Miocic S, Vatta M, Pinamonti B, Muntoni F, Caforio AL, McKenna WJ, Falaschi A, Giacca M, Camerini. Mestroni L, et al. Among authors: muntoni f. J Am Coll Cardiol. 1999 Jul;34(1):181-90. doi: 10.1016/s0735-1097(99)00172-2. J Am Coll Cardiol. 1999. PMID: 10400009 Free article.

10

Muscle histology vs MRI in Duchenne muscular dystrophy.

Kinali M, Arechavala-Gomeza V, Cirak S, Glover A, Guglieri M, Feng L, Hollingsworth KG, Hunt D, Jungbluth H, Roper HP, Quinlivan RM, Gosalakkal JA, Jayawant S, Nadeau A, Hughes-Carre L, Manzur AY, Mercuri E, Morgan JE, Straub V, Bushby K, Sewry C, Rutherford M, Muntoni F. Kinali M, et al. Among authors: muntoni f. Neurology. 2011 Jan 25;76(4):346-53. doi: 10.1212/WNL.0b013e318208811f. Neurology. 2011. PMID: 21263136 Free PMC article.

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