Poenaru L - Search Results

1

[Gaucher's and Fabry's diseases: biochemical and genetic aspects].

Caillaud C, Poenaru L. Caillaud C, et al. Among authors: poenaru l. J Soc Biol. 2002;196(2):135-40. J Soc Biol. 2002. PMID: 12360742 Review. French.

2

Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease.

Germain DP, Puech JP, Caillaud C, Kahn A, Poenaru L. Germain DP, et al. Among authors: poenaru l. Am J Hum Genet. 1998 Aug;63(2):415-27. doi: 10.1086/301969. Am J Hum Genet. 1998. PMID: 9683600 Free PMC article.

3

Gaucher disease in Romanian patients: incidence of the most common mutations and phenotypic manifestations.

Drugan C, Procopciuc L, Jebeleanu G, Grigorescu-Sido P, Dussau J, Poenaru L, Caillaud C. Drugan C, et al. Among authors: poenaru l. Eur J Hum Genet. 2002 Sep;10(9):511-5. doi: 10.1038/sj.ejhg.5200845. Eur J Hum Genet. 2002. PMID: 12173027

4

Bicistronic lentiviral vector corrects beta-hexosaminidase deficiency in transduced and cross-corrected human Sandhoff fibroblasts.

Arfi A, Bourgoin C, Basso L, Emiliani C, Tancini B, Chigorno V, Li YT, Orlacchio A, Poenaru L, Sonnino S, Caillaud C. Arfi A, et al. Among authors: poenaru l. Neurobiol Dis. 2005 Nov;20(2):583-93. doi: 10.1016/j.nbd.2005.04.017. Epub 2005 Jun 13. Neurobiol Dis. 2005. PMID: 15953731

5

Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A gene.

Draghia R, Letourneur F, Drugan C, Manicom J, Blanchot C, Kahn A, Poenaru L, Caillaud C. Draghia R, et al. Among authors: poenaru l. Hum Mutat. 1997;9(3):234-42. doi: 10.1002/(SICI)1098-1004(1997)9:3<234::AID-HUMU4>3.0.CO;2-7. Hum Mutat. 1997. PMID: 9090526

6

Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice.

Guidotti JE, Mignon A, Haase G, Caillaud C, McDonell N, Kahn A, Poenaru L. Guidotti JE, et al. Among authors: poenaru l. Hum Mol Genet. 1999 May;8(5):831-8. doi: 10.1093/hmg/8.5.831. Hum Mol Genet. 1999. PMID: 10196372

7

Gene therapy in lysosomal diseases.

Caillaud C, Poenaru L. Caillaud C, et al. Among authors: poenaru l. Biomed Pharmacother. 2000 Oct;54(10):505-12. doi: 10.1016/s0753-3322(00)00009-3. Biomed Pharmacother. 2000. PMID: 11130848 Review.

8

Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease.

Germain DP, Salard D, Fellmann F, Azibi K, Caillaud C, Bernard MC, Poenaru L. Germain DP, et al. Among authors: poenaru l. Hum Mutat. 2001 Apr;17(4):353. doi: 10.1002/humu.41. Hum Mutat. 2001. PMID: 11295840 No abstract available.

9

Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitol.

Bourgoin C, Emiliani C, Kremer EJ, Gelot A, Tancini B, Gravel RA, Drugan C, Orlacchio A, Poenaru L, Caillaud C. Bourgoin C, et al. Among authors: poenaru l. Gene Ther. 2003 Oct;10(21):1841-9. doi: 10.1038/sj.gt.3302081. Gene Ther. 2003. PMID: 12960974

10

Reversion of the biochemical defects in murine embryonic Sandhoff neurons using a bicistronic lentiviral vector encoding hexosaminidase alpha and beta.

Arfi A, Zisling R, Richard E, Batista L, Poenaru L, Futerman AH, Caillaud C. Arfi A, et al. Among authors: poenaru l. J Neurochem. 2006 Mar;96(6):1572-9. doi: 10.1111/j.1471-4159.2006.03665.x. Epub 2006 Jan 25. J Neurochem. 2006. PMID: 16441513 Free article.

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