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DiMauro

Showing results (811-820 of 942) with videos related to

Pageof 95
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Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
European Journal of Medical Genetics|September 5, 2016
Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletionHemant Varma, Phyllis L Faust, Alejandro D Iglesias, et al.
Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 5, 2019
Macrophage derived TNFα promotes hepatic reprogramming to Warburg-like metabolismTatyana N Tarasenko, Maxim Jestin, Shingo Matsumoto, et al.
Annals of Neurology|June 27, 2013
Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1Johanna Nilsson, Benedikt Schoser, Pascal Laforet, et al.
Neurology|April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiencyO Musumeci, A Naini, A E Slonim, et al.
Neurology|May 1, 1997
Mitochondrial encephalomyopathy with coenzyme Q10 deficiencyC Sobreira, M Hirano, S Shanske, et al.
Archives of Neurology|January 14, 2009
Protean phenotypic features of the A3243G mitochondrial DNA mutationPetra Kaufmann, Kristin Engelstad, Ying Wei, et al.
Optics Express|September 15, 2015
Laser induced periodic surface structure formation in germanium by strong field mid IR laser solid interaction at oblique incidenceDrake R Austin, Kyle R P Kafka, Simeon Trendafilov, et al.
Pageof 95

Showing results (811-820 of 942) with videos related to

Sort By:
Pageof 95
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
European Journal of Medical Genetics|September 5, 2016
Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletionHemant Varma, Phyllis L Faust, Alejandro D Iglesias, et al.
Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 5, 2019
Macrophage derived TNFα promotes hepatic reprogramming to Warburg-like metabolismTatyana N Tarasenko, Maxim Jestin, Shingo Matsumoto, et al.
Annals of Neurology|June 27, 2013
Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1Johanna Nilsson, Benedikt Schoser, Pascal Laforet, et al.
Neurology|April 11, 2001
Familial cerebellar ataxia with muscle coenzyme Q10 deficiencyO Musumeci, A Naini, A E Slonim, et al.
Neurology|May 1, 1997
Mitochondrial encephalomyopathy with coenzyme Q10 deficiencyC Sobreira, M Hirano, S Shanske, et al.
Archives of Neurology|January 14, 2009
Protean phenotypic features of the A3243G mitochondrial DNA mutationPetra Kaufmann, Kristin Engelstad, Ying Wei, et al.
Optics Express|September 15, 2015
Laser induced periodic surface structure formation in germanium by strong field mid IR laser solid interaction at oblique incidenceDrake R Austin, Kyle R P Kafka, Simeon Trendafilov, et al.
Pageof 95