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V Poole

Showing results (111-120 of 118) with videos related to

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European Journal of Neurology|March 19, 2019
Urogenital symptoms in mitochondrial disease: overlooked and undertreatedO V Poole, T Uchiyama, I Skorupinska, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2020
Primary mitochondrial diseases increase susceptibility to bipolar affective disorderAlessandro Colasanti, Enrico Bugiardini, Sami Amawi, et al.
Neurology. Genetics|February 12, 2020
Expanding the molecular and phenotypic spectrum of truncating <i>MT-ATP6</i> mutationsEnrico Bugiardini, Emanuela Bottani, Silvia Marchet, et al.
Cancer Medicine|June 3, 2021
The genomic landscape of teenage and young adult T-cell acute lymphoblastic leukemiaMarcela B Mansur, Caroline L Furness, Sirintra Nakjang, et al.
Human Molecular Genetics|May 1, 2019
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathyEnrico Bugiardini, Alice L Mitchell, Ilaria Dalla Rosa, et al.
Annals of Neurology|March 11, 2021
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological DiseasesOlivia V Poole, Chiara Pizzamiglio, David Murphy, et al.
Neurology. Genetics|May 17, 2017
Clinicopathologic and molecular spectrum of <i>RNASEH1</i>-related mitochondrial diseaseEnrico Bugiardini, Olivia V Poole, Andreea Manole, et al.
Physical Review Letters|April 22, 2014
Constraints on cosmic strings from the LIGO-Virgo gravitational-wave detectorsJ Aasi, J Abadie, B P Abbott, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
European Journal of Neurology|March 19, 2019
Urogenital symptoms in mitochondrial disease: overlooked and undertreatedO V Poole, T Uchiyama, I Skorupinska, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2020
Primary mitochondrial diseases increase susceptibility to bipolar affective disorderAlessandro Colasanti, Enrico Bugiardini, Sami Amawi, et al.
Neurology. Genetics|February 12, 2020
Expanding the molecular and phenotypic spectrum of truncating <i>MT-ATP6</i> mutationsEnrico Bugiardini, Emanuela Bottani, Silvia Marchet, et al.
Cancer Medicine|June 3, 2021
The genomic landscape of teenage and young adult T-cell acute lymphoblastic leukemiaMarcela B Mansur, Caroline L Furness, Sirintra Nakjang, et al.
Human Molecular Genetics|May 1, 2019
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathyEnrico Bugiardini, Alice L Mitchell, Ilaria Dalla Rosa, et al.
Annals of Neurology|March 11, 2021
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological DiseasesOlivia V Poole, Chiara Pizzamiglio, David Murphy, et al.
Neurology. Genetics|May 17, 2017
Clinicopathologic and molecular spectrum of <i>RNASEH1</i>-related mitochondrial diseaseEnrico Bugiardini, Olivia V Poole, Andreea Manole, et al.
Physical Review Letters|April 22, 2014
Constraints on cosmic strings from the LIGO-Virgo gravitational-wave detectorsJ Aasi, J Abadie, B P Abbott, et al.
Pageof 12