Mercuri E - Search Results

1

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. Neuropediatrics. 2002 Feb;33(1):10-4. doi: 10.1055/s-2002-23593. Neuropediatrics. 2002. PMID: 11930270

2

Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.

Mercuri E, Dubowitz L, Berardinelli A, Pennock J, Jongmans M, Henderson S, Muntoni F, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Neuropediatrics. 1995 Jun;26(3):156-62. doi: 10.1055/s-2007-979746. Neuropediatrics. 1995. PMID: 7477754

3

Neurological 'soft' signs may identify children with sickle cell disease who are at risk for stroke.

Mercuri E, Faundez JC, Roberts I, Flora S, Bouza H, Cowan F, Pennock J, Bydder G, Dubowitz L. Mercuri E, et al. Eur J Pediatr. 1995 Feb;154(2):150-6. Eur J Pediatr. 1995. PMID: 7720746

4

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.

Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Neuropediatrics. 1995 Feb;26(1):3-7. doi: 10.1055/s-2007-979711. Neuropediatrics. 1995. PMID: 7791947

5

The protein defect in congenital muscular dystrophy.

Sewry CA, Naom I, D'Alessandro M, Ferlini A, Philpot J, Mercuri E, Dubowitz V, Muntoni F. Sewry CA, et al. Among authors: mercuri e. Biochem Soc Trans. 1996 May;24(2):281S. doi: 10.1042/bst024281s. Biochem Soc Trans. 1996. PMID: 8736939 No abstract available.

6

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. Neuromuscul Disord. 1996 Dec;6(6):425-9. doi: 10.1016/s0960-8966(96)00383-5. Neuromuscul Disord. 1996. PMID: 9027850

7

Cerebellar infarction and atrophy in infants and children with a history of premature birth.

Mercuri E, He J, Curati WL, Dubowitz LM, Cowan FM, Bydder GM. Mercuri E, et al. Pediatr Radiol. 1997 Feb;27(2):139-43. doi: 10.1007/s002470050085. Pediatr Radiol. 1997. PMID: 9028846

8

Evaluation of the corpus callosum in clumsy children born prematurely: a functional and morphological study.

Mercuri E, Jongmans M, Henderson S, Pennock J, Chung YL, de Vries L, Dubowitz L. Mercuri E, et al. Neuropediatrics. 1996 Dec;27(6):317-22. doi: 10.1055/s-2007-973801. Neuropediatrics. 1996. PMID: 9050050

9

Visual function in full-term infants with hypoxic-ischaemic encephalopathy.

Mercuri E, Atkinson J, Braddick O, Anker S, Cowan F, Rutherford M, Pennock J, Dubowitz L. Mercuri E, et al. Neuropediatrics. 1997 Jun;28(3):155-61. doi: 10.1055/s-2007-973693. Neuropediatrics. 1997. PMID: 9266553

10

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. Pediatr Neurol. 1998 May;18(5):399-401. doi: 10.1016/s0887-8994(97)00222-1. Pediatr Neurol. 1998. PMID: 9650678

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