Muntoni F - Search Results

1

Respiratory management of congenital myasthenic syndromes in childhood: Workshop 8th December 2009, UCL Institute of Neurology, London, UK.

Robb SA, Muntoni F, Simonds AK. Robb SA, et al. Among authors: muntoni f. Neuromuscul Disord. 2010 Dec;20(12):833-8. doi: 10.1016/j.nmd.2010.08.002. Epub 2010 Sep 17. Neuromuscul Disord. 2010. PMID: 20850318 No abstract available.

2

Expression of laminin subunits in congenital muscular dystrophy.

Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni F, Dubowitz V. Sewry CA, et al. Among authors: muntoni f. Neuromuscul Disord. 1995 Jul;5(4):307-16. doi: 10.1016/0960-8966(94)00072-h. Neuromuscul Disord. 1995. PMID: 7580244

3

Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: a possible sequel of drug toxicity in first trimester of pregnancy?

Philpot J, Muntoni F, Skellett S, Dubowitz V. Philpot J, et al. Among authors: muntoni f. Neuromuscul Disord. 1995 Jan;5(1):67-9. doi: 10.1016/0960-8966(94)e0028-7. Neuromuscul Disord. 1995. PMID: 7719144

4

Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy.

Mercuri E, Pennock J, Goodwin F, Sewry C, Cowan F, Dubowitz L, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: muntoni f. Neuromuscul Disord. 1996 Dec;6(6):425-9. doi: 10.1016/s0960-8966(96)00383-5. Neuromuscul Disord. 1996. PMID: 9027850

5

Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.

Sewry CA, Taylor J, Anderson LV, Ozawa E, Pogue R, Piccolo F, Bushby K, Dubowitz V, Muntoni F. Sewry CA, et al. Among authors: muntoni f. Neuromuscul Disord. 1996 Dec;6(6):467-74. doi: 10.1016/s0960-8966(96)00389-6. Neuromuscul Disord. 1996. PMID: 9027857 Clinical Trial.

6

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.

Sewry CA, Naom I, D'Alessandro M, Sorokin L, Bruno S, Wilson LA, Dubowitz V, Muntoni F. Sewry CA, et al. Among authors: muntoni f. Neuromuscul Disord. 1997 May;7(3):169-75. doi: 10.1016/s0960-8966(97)00425-2. Neuromuscul Disord. 1997. PMID: 9185180

7

Prenatal diagnosis in merosin-deficient congenital muscular dystrophy.

Naom I, Sewry C, D'Alessandro M, Topaloglu H, Ferlini A, Wilson L, Dubowitz V, Muntoni F. Naom I, et al. Among authors: muntoni f. Neuromuscul Disord. 1997 May;7(3):176-9. doi: 10.1016/s0960-8966(97)00448-3. Neuromuscul Disord. 1997. PMID: 9185181

8

Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype.

Talbot K, Rodrigues NR, Ignatius J, Muntoni F, Davies KE. Talbot K, et al. Among authors: muntoni f. Neuromuscul Disord. 1997 May;7(3):198-201. doi: 10.1016/s0960-8966(97)00450-1. Neuromuscul Disord. 1997. PMID: 9185185

9

Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?

Taylor J, Muntoni F, Robb S, Dubowitz V, Sewry C. Taylor J, et al. Among authors: muntoni f. Neuromuscul Disord. 1997 Jun;7(4):211-6. doi: 10.1016/s0960-8966(97)00461-6. Neuromuscul Disord. 1997. PMID: 9196901

10

Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy.

Muntoni F, Lichtarowicz-Krynska EJ, Sewry CA, Manilal S, Recan D, Llense S, Taylor J, Morris GE, Dubowitz V. Muntoni F, et al. Neuromuscul Disord. 1998 Apr;8(2):72-6. doi: 10.1016/s0960-8966(98)00006-6. Neuromuscul Disord. 1998. PMID: 9608559

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