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DiMauro

Showing results (781-790 of 942) with videos related to

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Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
Archives of Neurology|February 10, 2010
A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromesBulent Kurt, Jaak Jaeken, Johan Van Hove, et al.
Bioorganic & Medicinal Chemistry Letters|February 10, 2012
Discovery and hit-to-lead optimization of pyrrolopyrimidines as potent, state-dependent Na(v)1.7 antagonistsNagasree Chakka, Howie Bregman, Bingfan Du, et al.
Neuromuscular Disorders : NMD|May 18, 2010
Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 geneHasan O Akman, Guido Davidzon, Kurenai Tanji, et al.
Spine Deformity|July 28, 2023
Does a dedicated "Scoliosis Team" and surgical standardization improve outcomes in adolescent idiopathic scoliosis surgery and is it reproducible?Vishal Sarwahi, Sayyida Hasan, Himanshu Rao, et al.
Nature Communications|June 16, 2026
Disentangling high harmonic generation from surface and bulk states of a topological insulatorSha Li, Wenyi Zhou, Kazi A Imroz, et al.
Nature Communications|May 5, 2023
High-order harmonic generation from a thin film crystal perturbed by a quasi-static terahertz fieldSha Li, Yaguo Tang, Lisa Ortmann, et al.
BMJ Open|March 28, 2013
Survival transcriptome in the coenzyme Q10 deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q10 deficienciesDaniel J M Fernández-Ayala, Ignacio Guerra, Sandra Jiménez-Gancedo, et al.
Scientific Reports|May 17, 2018
Structure-guided Discovery of Dual-recognition ChemibodiesAlan C Cheng, Elizabeth M Doherty, Sheree Johnstone, et al.
Neuromuscular Disorders : NMD|March 17, 2004
Fatal infantile neuromuscular presentation of glycogen storage disease type IVStacey K H Tay, Hasan O Akman, Wendy K Chung, et al.
Pageof 95

Showing results (781-790 of 942) with videos related to

Sort By:
Pageof 95
Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
Archives of Neurology|February 10, 2010
A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromesBulent Kurt, Jaak Jaeken, Johan Van Hove, et al.
Bioorganic & Medicinal Chemistry Letters|February 10, 2012
Discovery and hit-to-lead optimization of pyrrolopyrimidines as potent, state-dependent Na(v)1.7 antagonistsNagasree Chakka, Howie Bregman, Bingfan Du, et al.
Neuromuscular Disorders : NMD|May 18, 2010
Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 geneHasan O Akman, Guido Davidzon, Kurenai Tanji, et al.
Spine Deformity|July 28, 2023
Does a dedicated "Scoliosis Team" and surgical standardization improve outcomes in adolescent idiopathic scoliosis surgery and is it reproducible?Vishal Sarwahi, Sayyida Hasan, Himanshu Rao, et al.
Nature Communications|June 16, 2026
Disentangling high harmonic generation from surface and bulk states of a topological insulatorSha Li, Wenyi Zhou, Kazi A Imroz, et al.
Nature Communications|May 5, 2023
High-order harmonic generation from a thin film crystal perturbed by a quasi-static terahertz fieldSha Li, Yaguo Tang, Lisa Ortmann, et al.
BMJ Open|March 28, 2013
Survival transcriptome in the coenzyme Q10 deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q10 deficienciesDaniel J M Fernández-Ayala, Ignacio Guerra, Sandra Jiménez-Gancedo, et al.
Scientific Reports|May 17, 2018
Structure-guided Discovery of Dual-recognition ChemibodiesAlan C Cheng, Elizabeth M Doherty, Sheree Johnstone, et al.
Neuromuscular Disorders : NMD|March 17, 2004
Fatal infantile neuromuscular presentation of glycogen storage disease type IVStacey K H Tay, Hasan O Akman, Wendy K Chung, et al.
Pageof 95