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Louis Mandel

Showing results (101-110 of 221) with videos related to

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European Journal of Medical Genetics|September 20, 2019
Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in FranceVlad Titerlea, Doulaye Dembélé, Jean-Louis Mandel, et al.
Journal of the American Dental Association (1939)|November 26, 2019
Parotid swellings in an adolescentKun H Yoon, Scott Peters, Daria Vasilyeva, et al.
Journal of Neurology|July 8, 2025
Vertigo and dizziness in genetic neurodevelopmental disorders: an international cross-sectional studyChristophe Lopez, Pauline Burger, Jean-Louis Mandel, et al.
Human Molecular Genetics|August 20, 2003
Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatasesJocelyn Laporte, Florence Bedez, Alessandra Bolino, et al.
Medecine Sciences : M/S|December 25, 2007
[Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy]Anne Toussaint, Anne-Sophie Nicot, Jean-Louis Mandel, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Chronic submasseteric abscess: anatomic, radiologic, and pathologic featuresKevin C Jones, John Silver, William S Millar, et al.
Journal of Medical Systems|November 22, 2017
Cerberus, an Access Control Scheme for Enforcing Least Privilege in Patient Cohort Study Platforms : A Comprehensive Access Control Scheme Applied to the GENIDA Project - Study of Genetic Forms of Intellectual Disabilities and Autism Spectrum DisordersPierre Parrend, Timothée Mazzucotelli, Florent Colin, et al.
The Journal of Biological Chemistry|October 21, 2004
Hsp70 and Hsp40 chaperones do not modulate retinal phenotype in SCA7 miceDominique Helmlinger, Jacques Bonnet, Jean-Louis Mandel, et al.
Journal of the American Dental Association (1939)|March 26, 2019
Facial paralysis of unknown etiologyKevin C Lee, Jason J Lee, Scott M Peters, et al.
Molecular Biology of the Cell|November 14, 2008
Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assemblyMarie-Cécile Didiot, Murugan Subramanian, Eric Flatter, et al.
Pageof 23

Showing results (101-110 of 221) with videos related to

Sort By:
Pageof 23
European Journal of Medical Genetics|September 20, 2019
Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in FranceVlad Titerlea, Doulaye Dembélé, Jean-Louis Mandel, et al.
Journal of the American Dental Association (1939)|November 26, 2019
Parotid swellings in an adolescentKun H Yoon, Scott Peters, Daria Vasilyeva, et al.
Journal of Neurology|July 8, 2025
Vertigo and dizziness in genetic neurodevelopmental disorders: an international cross-sectional studyChristophe Lopez, Pauline Burger, Jean-Louis Mandel, et al.
Human Molecular Genetics|August 20, 2003
Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatasesJocelyn Laporte, Florence Bedez, Alessandra Bolino, et al.
Medecine Sciences : M/S|December 25, 2007
[Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy]Anne Toussaint, Anne-Sophie Nicot, Jean-Louis Mandel, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Chronic submasseteric abscess: anatomic, radiologic, and pathologic featuresKevin C Jones, John Silver, William S Millar, et al.
Journal of Medical Systems|November 22, 2017
Cerberus, an Access Control Scheme for Enforcing Least Privilege in Patient Cohort Study Platforms : A Comprehensive Access Control Scheme Applied to the GENIDA Project - Study of Genetic Forms of Intellectual Disabilities and Autism Spectrum DisordersPierre Parrend, Timothée Mazzucotelli, Florent Colin, et al.
The Journal of Biological Chemistry|October 21, 2004
Hsp70 and Hsp40 chaperones do not modulate retinal phenotype in SCA7 miceDominique Helmlinger, Jacques Bonnet, Jean-Louis Mandel, et al.
Journal of the American Dental Association (1939)|March 26, 2019
Facial paralysis of unknown etiologyKevin C Lee, Jason J Lee, Scott M Peters, et al.
Molecular Biology of the Cell|November 14, 2008
Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assemblyMarie-Cécile Didiot, Murugan Subramanian, Eric Flatter, et al.
Pageof 23