Livia Poënaru - Concepedia

Author

Livia Poënaru

Inserm

Also Known As

L Poenaru, L Poénaru, L. (a) Poenaru, L. (b) Poenaru, L. POENARU, L. Poenaru, Livia Poenaru, Livia Poënaru

118

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Inserm Université Paris Cité Institut Cochin Maternité Port Royal Centre National de la Recherche Scientifique

About

Livia Poënaru is an author at Inserm specializing in medicine, pathology, and pathogenesis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	32	1.7K
2	Natural Sciences	6	6	309
3	Public Health	4	4	137
4	Health Sciences	3	3	54
5	Engineering	1	1	13

Livia Poënaru

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Transfer of a foreign gene into the brain using adenovirus vectors Saïd Akli, Catherine Caillaud, Emmanuelle Vigne, Nature Genetics Foreign GeneGene TherapiesPathogenesisMolecular BiologyVirology	1993	534
Juvenile and adult-onset acid maltase deficiency in France Pascal Laforêt, Marc Nicolino, B. Eymard, Neurology	2000	213
Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragments Saïd Akli, Jamel Chelly, Jean‐Marc Lacorte, Genomics Molecular CharacterizationPcr-amplified Cdna FragmentsGenetic DisorderNatural SciencesGenetics	1991	101
A "G" to "A" mutation at position -1 of a 5' splice site in a late infantile form of Tay-Sachs disease. Saïd Akli, Jamel Chelly, Christine Mézard, Journal of Biological Chemistry Tay-sachs DiseasePoint Mutation GGeneticsPathologyMolecular Biology	1990	94
Electrophoretic study of hexosaminidases. Hexosaminidase C Livia Poënaru, J C Dreyfus Clinica Chimica Acta BiologyParasitologyParasitic ProtozoaHexosaminidase C	1973	90
Gene delivery into the central nervous system by nasal instillation in rats. R Draghia, Catherine Caillaud, R Manicom, PubMed	1995	83
Adenoviral Gene Therapy of the Tay-Sachs Disease in Hexosaminidase A-Deficient Knock-Out Mice Jacques‐Emmanuel Guidotti, Alexandre Mignon, G Haase, Human Molecular Genetics Tay-sachs DiseaseImmunologyPathologyImmunotherapyAntisense Therapy	1999	72
Gaucher Disease: The Origins of the Ashkenazi Jewish N370S and 84GG Acid β-Glucosidase Mutations George A. Díaz, Bruce D. Gelb, Neil Risch, The American Journal of Human Genetics Acid β-Glucosidase MutationsBiochemistryGeneticsInherited Metabolic DiseasePathogenesis	2000	72
Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease Michel Cohen‐Tannoudji, P. Marchand, Saïd Akli, Mammalian Genome ChromatinTay-sachs DiseaseMolecular NeuroscienceDevelopmental BiologyMendelian Disorder	1995	66
Absence of Hexosaminidase a and B in a Normal Adult Jean‐Claude Dreyfus, Livia Poënaru, Lars Svennerholm New England Journal of Medicine Autoimmune DiseaseBiochemistryGlycosylationGenetic DisorderArtificial Substrate	1975	66

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