Manzur AY - Search Results

1

Management of scoliosis in Duchenne muscular dystrophy: a large 10-year retrospective study.

Kinali M, Messina S, Mercuri E, Lehovsky J, Edge G, Manzur AY, Muntoni F. Kinali M, et al. Among authors: manzur ay. Dev Med Child Neurol. 2006 Jun;48(6):513-8. doi: 10.1017/S0012162206001083. Dev Med Child Neurol. 2006. PMID: 16700946 Free article.

2

A randomized controlled trial of early surgery in Duchenne muscular dystrophy.

Manzur AY, Hyde SA, Rodillo E, Heckmatt JZ, Bentley G, Dubowitz V. Manzur AY, et al. Neuromuscul Disord. 1992;2(5-6):379-87. doi: 10.1016/s0960-8966(06)80009-x. Neuromuscul Disord. 1992. PMID: 1300186 Clinical Trial.

3

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability.

Hodgson SV, Abbs S, Clark S, Manzur A, Heckmatt JZ, Dubowitz V, Bobrow M. Hodgson SV, et al. Neuromuscul Disord. 1992;2(4):269-76. doi: 10.1016/0960-8966(92)90059-f. Neuromuscul Disord. 1992. PMID: 1483053

4

Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.

Naom I, D'Alessandro M, Sewry CA, Philpot J, Manzur AY, Dubowitz V, Muntoni F. Naom I, et al. Among authors: manzur ay. Neuromuscul Disord. 1998 Oct;8(7):495-501. doi: 10.1016/s0960-8966(98)00065-0. Neuromuscul Disord. 1998. PMID: 9829280

5

Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2).

Mercuri E, Manzur AY, Jungbluth H, Bonne G, Muchir A, Sewry C, Schwartz K, Muntoni F. Mercuri E, et al. Among authors: manzur ay. Neurology. 2000 Apr 25;54(8):1704-5. doi: 10.1212/wnl.54.8.1704. Neurology. 2000. PMID: 10762524 No abstract available.

6

Minicore myopathy in children: a clinical and histopathological study of 19 cases.

Jungbluth H, Sewry C, Brown SC, Manzur AY, Mercuri E, Bushby K, Rowe P, Johnson MA, Hughes I, Kelsey A, Dubowitz V, Muntoni F. Jungbluth H, et al. Among authors: manzur ay. Neuromuscul Disord. 2000 Jun;10(4-5):264-73. doi: 10.1016/s0960-8966(99)00125-x. Neuromuscul Disord. 2000. PMID: 10838253

7

Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?

Mercuri E, Sewry CA, Brown SC, Brockington M, Jungbluth H, DeVile C, Counsell S, Manzur A, Muntoni F. Mercuri E, et al. Neuropediatrics. 2000 Aug;31(4):186-9. doi: 10.1055/s-2000-7460. Neuropediatrics. 2000. PMID: 11071142

8

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.

Jungbluth H, Müller CR, Halliger-Keller B, Brockington M, Brown SC, Feng L, Chattopadhyay A, Mercuri E, Manzur AY, Ferreiro A, Laing NG, Davis MR, Roper HP, Dubowitz V, Bydder G, Sewry CA, Muntoni F. Jungbluth H, et al. Among authors: manzur ay. Neurology. 2002 Jul 23;59(2):284-7. doi: 10.1212/wnl.59.2.284. Neurology. 2002. PMID: 12136074

9

Pilot trial of albuterol in spinal muscular atrophy.

Kinali M, Mercuri E, Main M, De Biasia F, Karatza A, Higgins R, Banks LM, Manzur AY, Muntoni F. Kinali M, et al. Among authors: manzur ay. Neurology. 2002 Aug 27;59(4):609-10. doi: 10.1212/wnl.59.4.609. Neurology. 2002. PMID: 12196659 Clinical Trial.

10

Early and severe presentation of X-linked myotubular myopathy in a girl with skewed X-inactivation.

Jungbluth H, Sewry CA, Buj-Bello A, Kristiansen M, Ørstavik KH, Kelsey A, Manzur AY, Mercuri E, Wallgren-Pettersson C, Muntoni F. Jungbluth H, et al. Among authors: manzur ay. Neuromuscul Disord. 2003 Jan;13(1):55-9. doi: 10.1016/s0960-8966(02)00194-3. Neuromuscul Disord. 2003. PMID: 12467733

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