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Results:
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Results: 8
Authors:
De Bruin, PF
Ueki, J
Bush, A
Manzur, AY
Watson, A
Pride, NB
Citation: Pf. De Bruin et al., Inspiratory flow reserve in boys with Duchenne muscular dystrophy, PEDIAT PULM, 31(6), 2001, pp. 451-457
Authors:
Jungbluth, H
Sewry, CA
Brown, SC
Nowak, KJ
Laing, NG
Wallgren-Pettersson, C
Pelin, K
Manzur, AY
Mercuri, E
Dubowitz, V
Muntoni, F
Citation: H. Jungbluth et al., Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene, NEUROMUSC D, 11(1), 2001, pp. 35-40
Authors:
Manzur, AY
Dubowitz, V
Citation: Ay. Manzur et V. Dubowitz, Muscular dystrophies, CONTEMPORARY TREATMENTS IN NEUROLOGY, 2001, pp. 264-282
Authors:
Jungbluth, H
Sewry, C
Brown, SC
Manzur, AY
Mercuri, E
Bushby, K
Rowe, P
Johnson, MA
Hughes, I
Kelsey, A
Dubowitz, V
Muntoni, F
Citation: H. Jungbluth et al., Minicore myopathy in children: a clinical and histopathological study of 19 cases, NEUROMUSC D, 10(4-5), 2000, pp. 264-273
Authors:
Jungbluth, H
Manzur, AY
Bydder, G
Muntoni, F
Citation: H. Jungbluth et al., Generalized calcification in a case of dermatomyositis, NEUROMUSC D, 10(2), 2000, pp. 150-150
Authors:
Mercuri, E
Manzur, AY
Jungbluth, H
Bonne, G
Muchir, A
Sewry, C
Schwartz, K
Muntoni, F
Citation: E. Mercuri et al., Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2), NEUROLOGY, 54(8), 2000, pp. 1704-1705
Authors:
Webb, DW
Jones, RR
Manzur, AY
Farrell, K
Citation: Dw. Webb et al., Retrospective study of late febrile seizures, PED NEUROL, 20(4), 1999, pp. 270-273
Authors:
Mercuri, E
Poulton, J
Buck, J
Broadbent, V
Bamford, M
Jungbluth, H
Manzur, AY
Muntoni, F
Citation: E. Mercuri et al., Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A, ARCH DIS CH, 81(5), 1999, pp. 442-443
Risultati:
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