The striking differences in the bioenergetics of brain and liver mitochondria are enhanced in mitochondrial disease

Authors: Balmaceda, Valeria ^a, Komlódi, Timea ^{b, e}, Szibor, Marten ^{c, d}, Gnaiger, Erich ^e, Moore, Anthony L. ^{f, ⁎, 1}, Fernandez-Vizarra, Erika ^{a, g, ⁎⁎, 1}, Viscomi, Carlo ^{a, g, ⁎⁎, 1}

Source: In BBA - Molecular Basis of Disease March 2024 1870(3)

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment

Authors: Parham Habibzadeh, Soroor Inaloo, Mohammad Silawi, Hassan Dastsooz, Mohammad Ali Farazi Fard, Forough Sadeghipour, Zahra Faghihi, Mohaddeseh Rezaeian, Majid Yavarian, Johann Böhm, Mohammad Ali Faghihi

Source: Frontiers in Neurology, Vol 10 (2019)

Subject Terms: mitochondrial diseases, mitochondrial encephalomyopathies, TTC19, mitochondrial complex III deficiency, neurodegenerative diseases, Neurology. Diseases of the nervous system, RC346-429

File Description: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fneur.2019.00944/full; https://doaj.org/toc/1664-2295

Access URL: https://doaj.org/article/d312bc71ba574865a1c9b67a15653618

Complex III deficiency due to an in-frame MT-CYB deletion presenting as ketotic hypoglycemia and lactic acidosis

Authors: Mari Mori, Jennifer Goldstein, Sarah P. Young, Edward H. Bossen, John Shoffner, Dwight D. Koeberl

Source: Molecular Genetics and Metabolism Reports, Vol 4, Iss C, Pp 39-41 (2015)

Subject Terms: Mitochondrial myopathy, Cytochrome b, Complex III deficiency, Ketotic hypoglycemia, Carnitine deficiency, Medicine (General), R5-920, Biology (General), QH301-705.5

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214426915300161; https://doaj.org/toc/2214-4269

Access URL: https://doaj.org/article/9eb665720dd54638bbbe8baae626be02

NUCLEAR GENE MUTATIONS AS THE CAUSE OF MITOCHONDRIAL COMPLEX III DEFICIENCY

Authors: Erika eFernandez-Vizarra, Massimo eZeviani

Source: Frontiers in Genetics, Vol 6 (2015)

Subject Terms: Mitochondrial Diseases, oxidative phosphorylation (OXPHOS), Genetic mutations, Complex III deficiency, Complex III assembly, Genetics, QH426-470

File Description: electronic resource

Relation: http://journal.frontiersin.org/Journal/10.3389/fgene.2015.00134/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/6b75d2d95ced4988a101e014a7cc7dd0

A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia and bilateral basal ganglia lesions

Authors: Laura eMelchionda, Nadirah S Damseh, Bassam Y Abu Libdeh, Alessia eNasca, Orly eElpeleg, Alice eZanolini, Daniele eGhezzi

Source: Frontiers in Genetics, Vol 5 (2014)

Subject Terms: Mitochondrial Diseases, novel mutations, Encephalomyopathy, Complex III deficiency, TTC19, Bilateral basal ganglia lesions, Genetics, QH426-470

File Description: electronic resource

Relation: http://journal.frontiersin.org/Journal/10.3389/fgene.2014.00397/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/fbefafdb8e38451289aae80a1356032c

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.

This result is not displayed to guests.
Login for full access.