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Movement Disorders : Official Journal of the Movement Disorder Society
|
April 16, 2023
Reply to: "Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort"
Marco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2021
A novel ALG14 missense variant in an alive child with myopathy, epilepsy, and progressive cerebral atrophy
Flavia Palombo, Benedetta Piccolo, Elena Saccani, et al.
Ophthalmology
|
February 24, 2016
Re: Pilat et al.: High-resolution imaging of the optic nerve and retina in optic nerve hypoplasia (Ophthalmology 2015;122:1330-9)
Piero Barboni, Giacomo Savini, Valerio Carelli, et al.
Ophthalmology
|
June 5, 2002
First application of extremely high-resolution magnetic resonance imaging to study microscopic features of normal and LHON human optic nerve
Alfredo A Sadun, Valerio Carelli, Swaraj Bose, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2003
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients
Elena Pegoraro, Andrea Vettori, Maria L Valentino, et al.
Frontiers in Neuroscience
|
June 14, 2019
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy
Rosamaria Santarelli, Chiara La Morgia, Maria Lucia Valentino, et al.
Melanoma Research
|
May 23, 2019
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin
Mariaelena Pistoni, Giulia Tondelli, Cristina Gallo, et al.
Biochimica Et Biophysica Acta. Bioenergetics
|
December 23, 2017
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III
Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 14, 2022
Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts
Marco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
The Journal of Biological Chemistry
|
December 14, 2001
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis
Steven R Danielson, Alice Wong, Valerio Carelli, et al.
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Showing results (71-80 of 371) with videos related to
Sort By:
Page
of 38
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 16, 2023
Reply to: "Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort"
Marco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2021
A novel ALG14 missense variant in an alive child with myopathy, epilepsy, and progressive cerebral atrophy
Flavia Palombo, Benedetta Piccolo, Elena Saccani, et al.
Ophthalmology
|
February 24, 2016
Re: Pilat et al.: High-resolution imaging of the optic nerve and retina in optic nerve hypoplasia (Ophthalmology 2015;122:1330-9)
Piero Barboni, Giacomo Savini, Valerio Carelli, et al.
Ophthalmology
|
June 5, 2002
First application of extremely high-resolution magnetic resonance imaging to study microscopic features of normal and LHON human optic nerve
Alfredo A Sadun, Valerio Carelli, Swaraj Bose, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2003
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients
Elena Pegoraro, Andrea Vettori, Maria L Valentino, et al.
Frontiers in Neuroscience
|
June 14, 2019
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy
Rosamaria Santarelli, Chiara La Morgia, Maria Lucia Valentino, et al.
Melanoma Research
|
May 23, 2019
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin
Mariaelena Pistoni, Giulia Tondelli, Cristina Gallo, et al.
Biochimica Et Biophysica Acta. Bioenergetics
|
December 23, 2017
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III
Concetta Valentina Tropeano, Jessica Fiori, Valerio Carelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 14, 2022
Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts
Marco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
The Journal of Biological Chemistry
|
December 14, 2001
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis
Steven R Danielson, Alice Wong, Valerio Carelli, et al.
Page
of 38