Bydder G - 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. Among authors: bydder g. Neuropediatrics. 2002 Feb;33(1):10-4. doi: 10.1055/s-2002-23593. Neuropediatrics. 2002. PMID: 11930270

2

A short protocol for muscle MRI in children with muscular dystrophies.

Mercuri E, Pichiecchio A, Counsell S, Allsop J, Cini C, Jungbluth H, Uggetti C, Bydder G. Mercuri E, et al. Among authors: bydder g. Eur J Paediatr Neurol. 2002;6(6):305-7. doi: 10.1016/s1090-3798(02)90617-3. Eur J Paediatr Neurol. 2002. PMID: 12401454

3

Magnetic resonance imaging of muscle in nemaline myopathy.

Jungbluth H, Sewry CA, Counsell S, Allsop J, Chattopadhyay A, Mercuri E, North K, Laing N, Bydder G, Pelin K, Wallgren-Pettersson C, Muntoni F. Jungbluth H, et al. Among authors: bydder g. Neuromuscul Disord. 2004 Dec;14(12):779-84. doi: 10.1016/j.nmd.2004.08.005. Neuromuscul Disord. 2004. PMID: 15564032

4

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: bydder g. Neuromuscul Disord. 1999 Mar;9(2):81-5. doi: 10.1016/s0960-8966(98)00110-2. Neuromuscul Disord. 1999. PMID: 10220862 Clinical Trial.

5

Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy.

Mercuri E, Rutherford M, De Vile C, Counsell S, Sewry C, Brown S, Bydder G, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: bydder g. Neuromuscul Disord. 2001 Apr;11(3):297-9. doi: 10.1016/s0960-8966(00)00190-5. Neuromuscul Disord. 2001. PMID: 11297945

6

Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?

Philpot J, Counsell S, Bydder G, Sewry CA, Dubowitz V, Muntoni F. Philpot J, et al. Among authors: bydder g. Neuromuscul Disord. 2001 Jul;11(5):489-93. doi: 10.1016/s0960-8966(00)00221-2. Neuromuscul Disord. 2001. PMID: 11404123

7

Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations.

Jungbluth H, Davis MR, Müller C, Counsell S, Allsop J, Chattopadhyay A, Messina S, Mercuri E, Laing NG, Sewry CA, Bydder G, Muntoni F. Jungbluth H, et al. Among authors: bydder g. Neuromuscul Disord. 2004 Dec;14(12):785-90. doi: 10.1016/j.nmd.2004.08.006. Neuromuscul Disord. 2004. PMID: 15564033

8

Early prognostic indicators of outcome in infants with neonatal cerebral infarction: a clinical, electroencephalogram, and magnetic resonance imaging study.

Mercuri E, Rutherford M, Cowan F, Pennock J, Counsell S, Papadimitriou M, Azzopardi D, Bydder G, Dubowitz L. Mercuri E, et al. Among authors: bydder g. Pediatrics. 1999 Jan;103(1):39-46. doi: 10.1542/peds.103.1.39. Pediatrics. 1999. PMID: 9917437

9

Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status.

Mercuri E, Gruter-Andrew J, Philpot J, Sewry C, Counsell S, Henderson S, Jensen A, Naom I, Bydder G, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: bydder g. Neuromuscul Disord. 1999 Oct;9(6-7):383-7. doi: 10.1016/s0960-8966(99)00034-6. Neuromuscul Disord. 1999. PMID: 10545041

10

Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.

Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F. Philpot J, et al. Among authors: bydder g. Eur J Paediatr Neurol. 2000;4(3):109-14. doi: 10.1053/ejpn.2000.0277. Eur J Paediatr Neurol. 2000. PMID: 10872105

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