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Journal of Neurology
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October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature
Gauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation
Irene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine
|
January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)
Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International
|
June 20, 2013
Mitochondrial fusion proteins and human diseases
Michela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
Developmental Medicine and Child Neurology
|
May 18, 2012
A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance
Romina Romaniello, Alessandra Tonelli, Filippo Arrigoni, et al.
Human Genetics
|
February 22, 2003
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot
Manuela Sironi, Uberto Pozzoli, Rachele Cagliani, et al.
Genome Research
|
May 3, 2003
Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature
Uberto Pozzoli, Greg Elgar, Rachele Cagliani, et al.
Genome Biology
|
September 27, 2008
The signature of long-standing balancing selection at the human defensin beta-1 promoter
Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
BMC Evolutionary Biology
|
June 21, 2011
Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolving
Rachele Cagliani, Stefania Riva, Uberto Pozzoli, et al.
BMC Neurology
|
August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations
Silvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Page
of 35
Search research articles
Search
Showing results (81-90 of 346) with videos related to
Sort By:
Page
of 35
Journal of Neurology
|
October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature
Gauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation
Irene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine
|
January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)
Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International
|
June 20, 2013
Mitochondrial fusion proteins and human diseases
Michela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
Developmental Medicine and Child Neurology
|
May 18, 2012
A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance
Romina Romaniello, Alessandra Tonelli, Filippo Arrigoni, et al.
Human Genetics
|
February 22, 2003
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot
Manuela Sironi, Uberto Pozzoli, Rachele Cagliani, et al.
Genome Research
|
May 3, 2003
Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature
Uberto Pozzoli, Greg Elgar, Rachele Cagliani, et al.
Genome Biology
|
September 27, 2008
The signature of long-standing balancing selection at the human defensin beta-1 promoter
Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
BMC Evolutionary Biology
|
June 21, 2011
Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolving
Rachele Cagliani, Stefania Riva, Uberto Pozzoli, et al.
BMC Neurology
|
August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations
Silvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Page
of 35