Manzur A - Search Results

1

Development of a functional assessment scale for ambulatory boys with Duchenne muscular dystrophy.

Scott E, Eagle M, Mayhew A, Freeman J, Main M, Sheehan J, Manzur A, Muntoni F; North Star Clinical Network for Paediatric Neuromuscular Disease. Scott E, et al. Among authors: manzur a. Physiother Res Int. 2012 Jun;17(2):101-9. doi: 10.1002/pri.520. Epub 2011 Sep 23. Physiother Res Int. 2012. PMID: 21954141

2

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

3

Generalized calcification in a case of dermatomyositis.

Jungbluth H, Manzur AY, Bydder G, Muntoni F. Jungbluth H, et al. Among authors: manzur ay. Neuromuscul Disord. 2000 Feb;10(2):150. doi: 10.1016/s0960-8966(99)00067-x. Neuromuscul Disord. 2000. PMID: 10714592 No abstract available.

4

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.

5

Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowing.

Bolland E, Manzur AY, Milward TM, Muntoni F. Bolland E, et al. Among authors: manzur ay. Eur J Paediatr Neurol. 2000;4(2):73-6. doi: 10.1053/ejpn.2000.0266. Eur J Paediatr Neurol. 2000. PMID: 10817488

6

An unusual case of hyperekplexia.

Jungbluth H, Rees MI, Manzur AY, Mercuri E, Sewry CA, Gobbi P, Muntoni F. Jungbluth H, et al. Among authors: manzur ay. Eur J Paediatr Neurol. 2000;4(2):77-80. doi: 10.1053/ejpn.1999.0267. Eur J Paediatr Neurol. 2000. PMID: 10817489

7

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

8

Muscular dystrophy campaign sponsored workshop: recommendation for respiratory care of children with spinal muscular atrophy type II and III. 13th February 2002, London, UK.

Manzur AY, Muntoni F, Simonds A. Manzur AY, et al. Neuromuscul Disord. 2003 Feb;13(2):184-9. doi: 10.1016/s0960-8966(02)00212-2. Neuromuscul Disord. 2003. PMID: 12565919 No abstract available.

9

Glucocorticoid corticosteroids for Duchenne muscular dystrophy.

Manzur AY, Kuntzer T, Pike M, Swan A. Manzur AY, et al. Cochrane Database Syst Rev. 2004;(2):CD003725. doi: 10.1002/14651858.CD003725.pub2. Cochrane Database Syst Rev. 2004. Update in: Cochrane Database Syst Rev. 2008 Jan 23;(1):CD003725. doi: 10.1002/14651858.CD003725.pub3. PMID: 15106215 Updated. Review.

10

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.

Kinali M, Jungbluth H, Eunson LH, Sewry CA, Manzur AY, Mercuri E, Hanna MG, Muntoni F. Kinali M, et al. Among authors: manzur ay. Neuromuscul Disord. 2004 Oct;14(10):689-93. doi: 10.1016/j.nmd.2004.06.007. Neuromuscul Disord. 2004. PMID: 15351427

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