Ionasescu VV - Search Results

1

Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) gene.

Ionasescu VV, Hart M, DiMauro S, Moraes CT. Ionasescu VV, et al. Neurology. 1994 May;44(5):975-7. doi: 10.1212/wnl.44.5.975. Neurology. 1994. PMID: 8190311

2

Comparison of ribosomal protein synthesis in Becker and Duchenne muscular dystrophies.

Ionasescu V, Zellweger H, McCormick WF, Conway TW. Ionasescu V, et al. Neurology. 1973 Mar;23(3):245-53. doi: 10.1212/wnl.23.3.245. Neurology. 1973. PMID: 4348618 No abstract available.

3

Recombinant DNA study of Duchenne muscular dystrophy occurring in a myotonic dystrophy family.

Ionasescu V, Searby C, Ionasescu R, Burns T. Ionasescu V, et al. Acta Neurol Scand. 1988 May;77(5):382-6. doi: 10.1111/j.1600-0404.1988.tb05923.x. Acta Neurol Scand. 1988. PMID: 3414375

4

Becker muscular dystrophy recombinant DNA studies in identical twins.

Ionasescu V, Ionasescu R, Searby C, Burns T. Ionasescu V, et al. Muscle Nerve. 1988 Apr;11(4):287-90. doi: 10.1002/mus.880110402. Muscle Nerve. 1988. PMID: 3398874

5

Localization of the gene for X-linked spinal muscular atrophy.

Fischbeck KH, Ionasescu V, Ritter AW, Ionasescu R, Davies K, Ball S, Bosch P, Burns T, Hausmanowa-Petrusewicz I, Borkowska J, et al. Fischbeck KH, et al. Neurology. 1986 Dec;36(12):1595-8. doi: 10.1212/wnl.36.12.1595. Neurology. 1986. PMID: 3466055

6

Identification of carriers of Duchenne muscular dystrophy by muscle protein synthesis.

Ionasescu V, Zellweger H, Shirk P, Conway TW. Ionasescu V, et al. Neurology. 1973 May;23(5):497-502. doi: 10.1212/wnl.23.5.497. Neurology. 1973. PMID: 4735465 No abstract available.

7

A new approach for carrier detection in Duchenne muscular dystrophy. Protein synthesis of muscle polyribosomes in vitro.

Ionasescu V, Zellweger H, Conway TW. Ionasescu V, et al. Neurology. 1971 Jul;21(7):703-9. doi: 10.1212/wnl.21.7.703. Neurology. 1971. PMID: 4327312 No abstract available.

8

X-linked Charcot-Marie-Tooth disease and connexin32.

Ionasescu VV. Ionasescu VV. Cell Biol Int. 1998 Nov;22(11-12):807-13. doi: 10.1006/cbir.1998.0387. Cell Biol Int. 1998. PMID: 10873293

9

Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene.

Ionasescu VV, Searby CC, Ionasescu R, Reisin R, Ruggieri V, Arberas C. Ionasescu VV, et al. Muscle Nerve. 1997 Oct;20(10):1308-10. doi: 10.1002/(sici)1097-4598(199710)20:10<1308::aid-mus14>3.0.co;2-z. Muscle Nerve. 1997. PMID: 9324088

10

Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene.

Ionasescu VV, Searby CC, Ionasescu R, Chatkupt S, Patel N, Koenigsberger R. Ionasescu VV, et al. Muscle Nerve. 1997 Jan;20(1):97-9. doi: 10.1002/(sici)1097-4598(199701)20:1<97::aid-mus13>3.0.co;2-z. Muscle Nerve. 1997. PMID: 8995589

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