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Irène Maire

Showing results (1-10 of 15) with videos related to

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Bulletin De L'Academie Nationale De Medecine|December 10, 2013
[Lysosomal proteolysis; overview of lysosomal diseases]Irène Maire
Presse Medicale (Paris, France : 1983)|June 5, 2007
[Lysosomal storage diseases: functional classification and treatment principles]Irène Maire
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2007
Mucopolysaccharidosis type II: an update on mutation spectrumRoseline Froissart, Isabel Moreira Da Silva, Irène Maire
Brain & Development|February 18, 2006
Type 2 Gaucher disease: 15 new cases and review of the literatureCyril Mignot, Diana Doummar, Irène Maire, et al.
Human Mutation|October 1, 2003
Molecular pathology of NEU1 gene in sialidosisVolkan Seyrantepe, Helena Poupetova, Roseline Froissart, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 13, 2004
Improved behavior and neuropathology in the mouse model of Sanfilippo type IIIB disease after adeno-associated virus-mediated gene transfer in the striatumArnaud Cressant, Nathalie Desmaris, Lucie Verot, et al.
Chronobiology International|September 5, 2009
Liver circadian clock, a pharmacologic target of cyclin-dependent kinase inhibitor seliciclibIda Iurisci, Elisabeth Filipski, Hatem Sallam, et al.
Molecular Genetics and Metabolism|March 8, 2008
Abnormal expression of truncated CRMP-1 protein in the brain cortex of MPSIIIB miceDavid Cheillan, Céline Malleval, Jérôme Ausseil, et al.
Annales De Biologie Clinique|July 24, 2010
[Metachromatic leucodystrophy. Clinical, biological, and therapeutic aspects]Ilhem Barboura, Salima Ferchichi, Azza Dandana, et al.
Journal of the Peripheral Nervous System : JPNS|June 22, 2006
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutationsPhilippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Bulletin De L'Academie Nationale De Medecine|December 10, 2013
[Lysosomal proteolysis; overview of lysosomal diseases]Irène Maire
Presse Medicale (Paris, France : 1983)|June 5, 2007
[Lysosomal storage diseases: functional classification and treatment principles]Irène Maire
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2007
Mucopolysaccharidosis type II: an update on mutation spectrumRoseline Froissart, Isabel Moreira Da Silva, Irène Maire
Brain & Development|February 18, 2006
Type 2 Gaucher disease: 15 new cases and review of the literatureCyril Mignot, Diana Doummar, Irène Maire, et al.
Human Mutation|October 1, 2003
Molecular pathology of NEU1 gene in sialidosisVolkan Seyrantepe, Helena Poupetova, Roseline Froissart, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 13, 2004
Improved behavior and neuropathology in the mouse model of Sanfilippo type IIIB disease after adeno-associated virus-mediated gene transfer in the striatumArnaud Cressant, Nathalie Desmaris, Lucie Verot, et al.
Chronobiology International|September 5, 2009
Liver circadian clock, a pharmacologic target of cyclin-dependent kinase inhibitor seliciclibIda Iurisci, Elisabeth Filipski, Hatem Sallam, et al.
Molecular Genetics and Metabolism|March 8, 2008
Abnormal expression of truncated CRMP-1 protein in the brain cortex of MPSIIIB miceDavid Cheillan, Céline Malleval, Jérôme Ausseil, et al.
Annales De Biologie Clinique|July 24, 2010
[Metachromatic leucodystrophy. Clinical, biological, and therapeutic aspects]Ilhem Barboura, Salima Ferchichi, Azza Dandana, et al.
Journal of the Peripheral Nervous System : JPNS|June 22, 2006
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutationsPhilippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, et al.
Pageof 2