Search research articles
Contact Us
Filters
Showing results (41-50 of 59) with videos related to
Page
of 6
Sort By:
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 males
I Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG
|
June 15, 2000
Preserved speech variant is allelic of classic Rett syndrome
C 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 pain
D 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 spasms
E 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 cells
M 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 Africans
B Longo-Mbenza, M Mvitu Muaka, E Cibanda Yokobo, et al.
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I 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 patients
I Longo, S G M Frints, J-P Fryns, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C Pescucci, R Caselli, F Mari, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 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 males
I Meloni, M Bruttini, I Longo, et al.
European Journal of Human Genetics : EJHG
|
June 15, 2000
Preserved speech variant is allelic of classic Rett syndrome
C 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 pain
D 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 spasms
E 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 cells
M 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 Africans
B Longo-Mbenza, M Mvitu Muaka, E Cibanda Yokobo, et al.
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I 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 patients
I Longo, S G M Frints, J-P Fryns, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C Pescucci, R Caselli, F Mari, et al.
Page
of 6