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Solenn Legallic

Showing results (1-10 of 12) with videos related to

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Journal of Alzheimer'S Disease : JAD|July 17, 2010
Frontotemporal dementia phenotype associated with MAPT gene duplicationAnne Rovelet-Lecrux, Didier Hannequin, Olivier Guillin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 9, 2008
No pathogenic rearrangement within the DISC 1 gene in psychosisSolenn Legallic, Jacqueline Bou, Sadeq Haouzir, et al.
Psychiatric Genetics|January 17, 2008
Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardationGabriella Di Rosa, Giuseppina Pustorino, Maria Spano, et al.
Neurobiology of Disease|May 16, 2008
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson diseaseAnne Rovelet-Lecrux, Vincent Deramecourt, Solenn Legallic, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Psychiatric Genetics|August 31, 2007
ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophreniaCaroline Demily, Solenn Legallic, Jacqueline Bou, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseAnne Rovelet-Lecrux, Solenn Legallic, David Wallon, et al.
Neurology|December 21, 2012
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, David Maltête, et al.
Human Mutation|June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlationsAudrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Archives of General Psychiatry|September 9, 2009
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationAudrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Alzheimer'S Disease : JAD|July 17, 2010
Frontotemporal dementia phenotype associated with MAPT gene duplicationAnne Rovelet-Lecrux, Didier Hannequin, Olivier Guillin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 9, 2008
No pathogenic rearrangement within the DISC 1 gene in psychosisSolenn Legallic, Jacqueline Bou, Sadeq Haouzir, et al.
Psychiatric Genetics|January 17, 2008
Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardationGabriella Di Rosa, Giuseppina Pustorino, Maria Spano, et al.
Neurobiology of Disease|May 16, 2008
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson diseaseAnne Rovelet-Lecrux, Vincent Deramecourt, Solenn Legallic, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Psychiatric Genetics|August 31, 2007
ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophreniaCaroline Demily, Solenn Legallic, Jacqueline Bou, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseAnne Rovelet-Lecrux, Solenn Legallic, David Wallon, et al.
Neurology|December 21, 2012
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, David Maltête, et al.
Human Mutation|June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlationsAudrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Archives of General Psychiatry|September 9, 2009
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationAudrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, et al.
Pageof 2