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Dennis A Stephenson

Showing results (1-10 of 7) with videos related to

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Current Opinion in Neurology|March 14, 2007
Recent developments in neurofibromatosis type 1Ming-Jen Lee, Dennis A Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2012
Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemiaMing-Jen Lee, Kuo-Liong Chien, Ming-Fong Chen, et al.
Journal of Neurology|February 13, 2007
Characterization of a familial case with primary erythromelalgia from TaiwanMing-Jen Lee, Hsin-Su Yu, Sung-Tsang Hsieh, et al.
Human Mutation|July 13, 2006
Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1Ming-Jen Lee, Yi-Ning Su, Huey-Ling You, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 17, 2014
Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor miceSarah R Anderson, Inyoul Lee, Christine Ebeling, et al.
Human Molecular Genetics|July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) geneMing-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Cerebellum (London, England)|June 25, 2011
Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findingsHeike Jacobi, Till-Karsten Hauser, Paola Giunti, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Current Opinion in Neurology|March 14, 2007
Recent developments in neurofibromatosis type 1Ming-Jen Lee, Dennis A Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2012
Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemiaMing-Jen Lee, Kuo-Liong Chien, Ming-Fong Chen, et al.
Journal of Neurology|February 13, 2007
Characterization of a familial case with primary erythromelalgia from TaiwanMing-Jen Lee, Hsin-Su Yu, Sung-Tsang Hsieh, et al.
Human Mutation|July 13, 2006
Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1Ming-Jen Lee, Yi-Ning Su, Huey-Ling You, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 17, 2014
Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor miceSarah R Anderson, Inyoul Lee, Christine Ebeling, et al.
Human Molecular Genetics|July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) geneMing-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Cerebellum (London, England)|June 25, 2011
Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findingsHeike Jacobi, Till-Karsten Hauser, Paola Giunti, et al.
Pageof 1