Manzur AY - Search Results

1

Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom.

Maggi L, Scoto M, Cirak S, Robb SA, Klein A, Lillis S, Cullup T, Feng L, Manzur AY, Sewry CA, Abbs S, Jungbluth H, Muntoni F. Maggi L, et al. Among authors: manzur ay. Neuromuscul Disord. 2013 Mar;23(3):195-205. doi: 10.1016/j.nmd.2013.01.004. Epub 2013 Feb 8. Neuromuscul Disord. 2013. PMID: 23394784

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

A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance.

Manzur AY, Sewry CA, Ziprin J, Dubowitz V, Muntoni F. Manzur AY, et al. Neuromuscul Disord. 1998 Oct;8(7):467-73. doi: 10.1016/s0960-8966(98)00064-9. Neuromuscul Disord. 1998. PMID: 9829276

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

Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A.

Mercuri E, Poulton J, Buck J, Broadbent V, Bamford M, Jungbluth H, Manzur AY, Muntoni F. Mercuri E, et al. Among authors: manzur ay. Arch Dis Child. 1999 Nov;81(5):442-3. doi: 10.1136/adc.81.5.442. Arch Dis Child. 1999. PMID: 10519723 Free PMC article.

6

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.

7

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.

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

111 results

Search Page

Filters