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Movement Disorders : Official Journal of the Movement Disorder Society
|
July 6, 2022
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study
Marco Percetti, Giulia Franco, Edoardo Monfrini, et al.
Scientific Reports
|
July 24, 2025
The origin of modern North Africans as depicted by a massive survey of mitogenomes
Giulia Colombo, Elisabetta Moroni, Alessandro Raveane, et al.
American Journal of Ophthalmology
|
December 10, 2022
Safety of Lenadogene Nolparvovec Gene Therapy Over 5 Years in 189 Patients With Leber Hereditary Optic Neuropathy
Catherine Vignal-Clermont, Patrick Yu-Wai-Man, Nancy J Newman, et al.
Human Mutation
|
May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance
Valeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Science Advances
|
July 3, 2021
The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replication
Min Jiang, Xie Xie, Xuefeng Zhu, et al.
Scientific Reports
|
March 18, 2020
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
Chiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Neurogenetics
|
January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey
Chiara Ticci, Federico Sicca, Anna Ardissone, et al.
Ophthalmology
|
February 16, 2017
Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series
Tiffany Jean Hwang, Rustum Karanjia, Milton Nunes Moraes-Filho, et al.
Frontiers in Neurology
|
June 10, 2021
Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A <i>ND4</i> Mutation: Systematic Review and Indirect Comparison
Nancy J Newman, Patrick Yu-Wai-Man, Valerio Carelli, et al.
Scientific Reports
|
June 25, 2020
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
Chiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
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of 34
Search research articles
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Showing results (271-280 of 332) with videos related to
Sort By:
Page
of 34
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 6, 2022
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study
Marco Percetti, Giulia Franco, Edoardo Monfrini, et al.
Scientific Reports
|
July 24, 2025
The origin of modern North Africans as depicted by a massive survey of mitogenomes
Giulia Colombo, Elisabetta Moroni, Alessandro Raveane, et al.
American Journal of Ophthalmology
|
December 10, 2022
Safety of Lenadogene Nolparvovec Gene Therapy Over 5 Years in 189 Patients With Leber Hereditary Optic Neuropathy
Catherine Vignal-Clermont, Patrick Yu-Wai-Man, Nancy J Newman, et al.
Human Mutation
|
May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance
Valeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Science Advances
|
July 3, 2021
The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replication
Min Jiang, Xie Xie, Xuefeng Zhu, et al.
Scientific Reports
|
March 18, 2020
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
Chiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Neurogenetics
|
January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey
Chiara Ticci, Federico Sicca, Anna Ardissone, et al.
Ophthalmology
|
February 16, 2017
Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series
Tiffany Jean Hwang, Rustum Karanjia, Milton Nunes Moraes-Filho, et al.
Frontiers in Neurology
|
June 10, 2021
Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A <i>ND4</i> Mutation: Systematic Review and Indirect Comparison
Nancy J Newman, Patrick Yu-Wai-Man, Valerio Carelli, et al.
Scientific Reports
|
June 25, 2020
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
Chiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Page
of 34