Search research articles
Contact Us
Filters
Showing results (91-100 of 95) with videos related to
Page
of 10
Sort By:
You have reached the last page of results.
This site can display upto 95 results.
The New England Journal of Medicine
|
July 17, 2025
Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA Disease
Louise A Hyslop, Emma L Blakely, Magomet Aushev, et al.
Brain : a Journal of Neurology
|
December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial disease
Yi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
Brain : a Journal of Neurology
|
April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
Gerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
Ebiomedicine
|
March 7, 2018
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Yi Shiau Ng, Nichola Z Lax, Paul Maddison, et al.
Nature Communications
|
February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological disease
Monika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 95) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 95 results.
The New England Journal of Medicine
|
July 17, 2025
Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA Disease
Louise A Hyslop, Emma L Blakely, Magomet Aushev, et al.
Brain : a Journal of Neurology
|
December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial disease
Yi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
Brain : a Journal of Neurology
|
April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
Gerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
Ebiomedicine
|
March 7, 2018
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Yi Shiau Ng, Nichola Z Lax, Paul Maddison, et al.
Nature Communications
|
February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological disease
Monika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
Page
of 10