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Sara Shanske

Showing results (21-30 of 45) with videos related to

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Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Headache|June 24, 2004
Study of mitochondrial DNA mutations in patients with migraine with prolonged auraTodd D Rozen, Sara Shanske, David Otaegui, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNACharalampos L Karadimas, Leonardo Salviati, Sabrina Sacconi, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Journal of Child Neurology|May 28, 2004
Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathyCigdem Inan Akman, Carolyn M Sue, Sara Shanske, et al.
Journal of Child Neurology|March 30, 2005
Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNAStacey K H Tay, Sara Shanske, Carol Crowe, et al.
Archives of Neurology|December 15, 2004
Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiencyStacey K H Tay, Claudia Nesti, Michelangelo Mancuso, et al.
American Journal of Medical Genetics. Part A|March 3, 2009
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELASMahsa Mehrazin, Sara Shanske, Petra Kaufmann, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Archives of Neurology|March 12, 2008
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 casesSara Shanske, Jorida Coku, Jiesheng Lu, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Headache|June 24, 2004
Study of mitochondrial DNA mutations in patients with migraine with prolonged auraTodd D Rozen, Sara Shanske, David Otaegui, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNACharalampos L Karadimas, Leonardo Salviati, Sabrina Sacconi, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Journal of Child Neurology|May 28, 2004
Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathyCigdem Inan Akman, Carolyn M Sue, Sara Shanske, et al.
Journal of Child Neurology|March 30, 2005
Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNAStacey K H Tay, Sara Shanske, Carol Crowe, et al.
Archives of Neurology|December 15, 2004
Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiencyStacey K H Tay, Claudia Nesti, Michelangelo Mancuso, et al.
American Journal of Medical Genetics. Part A|March 3, 2009
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELASMahsa Mehrazin, Sara Shanske, Petra Kaufmann, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Archives of Neurology|March 12, 2008
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 casesSara Shanske, Jorida Coku, Jiesheng Lu, et al.
Pageof 5