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I Longo

Showing results (41-50 of 59) with videos related to

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American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
Photomedicine and Laser Surgery|May 25, 2005
Analgesic effect of He-Ne (632.8 nm) low-level laser therapy on acute inflammatory painD M Ferreira, R A Zângaro, A Balbin Villaverde, et al.
Brain & Development|June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)A Renieri, F Mari, M A Mencarelli, et al.
Journal of Medical Genetics|February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasmsE Scala, F Ariani, F Mari, et al.
The Journal of Biological Chemistry|September 26, 2001
Expression of functional chemokine receptors CXCR3 and CXCR4 on human melanoma cellsM M Robledo, R A Bartolome, N Longo, et al.
Molecular Vision|July 10, 2012
Effects of biomarkers of oxidative stress damage on prevalence and severity of visual disability among black Central AfricansB Longo-Mbenza, M Mvitu Muaka, E Cibanda Yokobo, et al.
Neuroscience|January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architectureI Meloni, V Parri, R De Filippis, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
Human Mutation|September 20, 2006
The Italian XLMR bank: a clinical and molecular databaseC Pescucci, R Caselli, F Mari, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
Photomedicine and Laser Surgery|May 25, 2005
Analgesic effect of He-Ne (632.8 nm) low-level laser therapy on acute inflammatory painD M Ferreira, R A Zângaro, A Balbin Villaverde, et al.
Brain & Development|June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)A Renieri, F Mari, M A Mencarelli, et al.
Journal of Medical Genetics|February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasmsE Scala, F Ariani, F Mari, et al.
The Journal of Biological Chemistry|September 26, 2001
Expression of functional chemokine receptors CXCR3 and CXCR4 on human melanoma cellsM M Robledo, R A Bartolome, N Longo, et al.
Molecular Vision|July 10, 2012
Effects of biomarkers of oxidative stress damage on prevalence and severity of visual disability among black Central AfricansB Longo-Mbenza, M Mvitu Muaka, E Cibanda Yokobo, et al.
Neuroscience|January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architectureI Meloni, V Parri, R De Filippis, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
Human Mutation|September 20, 2006
The Italian XLMR bank: a clinical and molecular databaseC Pescucci, R Caselli, F Mari, et al.
Pageof 6