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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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F Piemonte

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Neurology|March 14, 2001

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.

Neuromuscular Disorders : NMD|August 30, 2001

Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.

Clinical Genetics|July 28, 2016

DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7M Di Nottia, M Masciullo, D Verrigni, et al.

Clinical Genetics|April 23, 2016

A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.

Pageof 4

Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Neurology|March 14, 2001

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.

Neuromuscular Disorders : NMD|August 30, 2001

Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.

Clinical Genetics|July 28, 2016

DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7M Di Nottia, M Masciullo, D Verrigni, et al.

Clinical Genetics|April 23, 2016

A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.

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