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Jorida Coku

Showing results (1-10 of 14) with videos related to

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Pediatric Cardiology|September 4, 2007
Kearns-Sayre syndrome presenting as complete heart blockSanjay Chawla, Jorida Coku, Thomas Forbes, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Neuromuscular Disorders : NMD|March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegiaEvangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Plos Computational Biology|October 13, 2017
Systematic, network-based characterization of therapeutic target inhibitorsYao Shen, Mariano J Alvarez, Brygida Bisikirska, et al.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Mitochondrial myopathy associated with a novel mutation in mtDNAJacklyn Pancrudo, Sara Shanske, Jorida Coku, 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.
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.
Neuromuscular Disorders : NMD|May 28, 2008
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B geneBelén Bornstein, Estela Area, Kevin M Flanigan, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Pediatric Cardiology|September 4, 2007
Kearns-Sayre syndrome presenting as complete heart blockSanjay Chawla, Jorida Coku, Thomas Forbes, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Neuromuscular Disorders : NMD|March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegiaEvangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Plos Computational Biology|October 13, 2017
Systematic, network-based characterization of therapeutic target inhibitorsYao Shen, Mariano J Alvarez, Brygida Bisikirska, et al.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Mitochondrial myopathy associated with a novel mutation in mtDNAJacklyn Pancrudo, Sara Shanske, Jorida Coku, 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.
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.
Neuromuscular Disorders : NMD|May 28, 2008
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B geneBelén Bornstein, Estela Area, Kevin M Flanigan, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pageof 2