Dubowitz V - Search Results

1

68th ENMC international workshop (5th international workshop): On congenital muscular dystrophy, 9-11 April 1999, Naarden, The Netherlands.

Dubowitz V. Dubowitz V. Neuromuscul Disord. 1999 Oct;9(6-7):446-54. doi: 10.1016/s0960-8966(99)00074-7. Neuromuscul Disord. 1999. PMID: 10545052 No abstract available.

2

Prenatal diagnosis in congenital muscular dystrophy.

Muntoni F, Sewry C, Wilson L, Angelini C, Trevisan CP, Brambati B, Dubowitz V. Muntoni F, et al. Among authors: dubowitz v. Lancet. 1995 Mar 4;345(8949):591. doi: 10.1016/s0140-6736(95)90504-9. Lancet. 1995. PMID: 7776805 No abstract available.

3

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. Among authors: dubowitz v. Neuromuscul Disord. 1992;2(5-6):379-87. doi: 10.1016/s0960-8966(06)80009-x. Neuromuscul Disord. 1992. PMID: 1300186 Clinical Trial.

4

Prednisone in Duchenne dystrophy.

Dubowitz V. Dubowitz V. Neuromuscul Disord. 1991;1(3):161-3. doi: 10.1016/0960-8966(91)90019-o. Neuromuscul Disord. 1991. PMID: 1822789 Review. No abstract available.

5

Cardiac transplantation in Becker muscular dystrophy.

Quinlivan RM, Dubowitz V. Quinlivan RM, et al. Among authors: dubowitz v. Neuromuscul Disord. 1992;2(3):165-7. doi: 10.1016/0960-8966(92)90002-n. Neuromuscul Disord. 1992. PMID: 1483041 Review.

6

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. Among authors: dubowitz v. Neuromuscul Disord. 1992;2(4):269-76. doi: 10.1016/0960-8966(92)90059-f. Neuromuscul Disord. 1992. PMID: 1483053

7

What's in a name? Muscular dystrophy revisited.

Dubowitz V. Dubowitz V. Eur J Paediatr Neurol. 1998;2(6):279-84. doi: 10.1016/s1090-3798(98)80001-9. Eur J Paediatr Neurol. 1998. PMID: 10727193 Review. No abstract available.

8

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.

Wallgren-Pettersson C, Pelin K, Hilpelä P, Donner K, Porfirio B, Graziano C, Swoboda KJ, Fardeau M, Urtizberea JA, Muntoni F, Sewry C, Dubowitz V, Iannaccone S, Minetti C, Pedemonte M, Seri M, Cusano R, Lammens M, Castagna-Sloane A, Beggs AH, Laing NG, de la Chapelle A. Wallgren-Pettersson C, et al. Among authors: dubowitz v. Neuromuscul Disord. 1999 Dec;9(8):564-72. doi: 10.1016/s0960-8966(99)00061-9. Neuromuscul Disord. 1999. PMID: 10619714

9

A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis.

Wallgren-Pettersson C, Avela K, Marchand S, Kolehmainen J, Tahvanainen E, Hansen FJ, Muntoni F, Dubowitz V, De Visser M, Van Langen IM, et al. Wallgren-Pettersson C, et al. Among authors: dubowitz v. Neuromuscul Disord. 1995 Nov;5(6):441-3. doi: 10.1016/0960-8966(95)00022-f. Neuromuscul Disord. 1995. PMID: 8580725

10

Duchenne muscular dystrophy: Ringo to the rescue?

Cohn RD, Dubowitz V. Cohn RD, et al. Among authors: dubowitz v. Neuromuscul Disord. 2016 Jan;26(1):5-6. doi: 10.1016/j.nmd.2015.12.001. Neuromuscul Disord. 2016. PMID: 26801251 No abstract available.

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

Search Page

Search Results