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Scientific Reports
|
November 17, 2017
Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency
Syeda T Ahmed, Charlotte L Alston, Sila Hopton, et al.
Journal of Rare Diseases (Berlin, Germany)
|
August 11, 2025
Severe clinical manifestation of mitochondrial disease due to the m.3243A>T variant: a case report of early-onset, multi-organ involvement and premature death
Hannah Gillespie, Yi Shiau Ng, Katrina M Wood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations
Helen R Griffin, Angela Pyle, Emma L Blakely, et al.
The Cancer Journal From Scientific American
|
March 1, 1996
The accumulation of multiple genetic abnormalities in individual tumor cells in human breast cancers: clinical prognostic implications
S E Shackney, A A Pollice, C A Smith, et al.
The Journal of Infectious Diseases
|
May 15, 2020
Hepatitis C Virus (HCV) Direct-Acting Antiviral Therapy in Persons With Human Immunodeficiency Virus-HCV Genotype 1 Coinfection Resulting in High Rate of Sustained Virologic Response and Variable in Normalization of Soluble Markers of Immune Activation
Donald D Anthony, Mark S Sulkowski, Laura M Smeaton, et al.
JAMA Neurology
|
April 26, 2016
Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
Mika H Martikainen, Yi Shiau Ng, Gráinne S Gorman, et al.
Antiviral Therapy
|
February 17, 2007
Safety and efficacy of extended-release niacin for the treatment of dyslipidaemia in patients with HIV infection: AIDS Clinical Trials Group Study A5148
Michael P Dubé, Julia W Wu, Judith A Aberg, et al.
AIDS Research and Human Retroviruses
|
October 13, 2005
A randomized trial of the efficacy and safety of fenofibrate versus pravastatin in HIV-infected subjects with lipid abnormalities: AIDS Clinical Trials Group Study 5087
Judith A Aberg, Robert A Zackin, Susan W Brobst, et al.
Neurogenetics
|
November 25, 2014
A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Michael J Keogh, D Daud, A Pyle, et al.
Biochimica Et Biophysica Acta
|
October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
Abdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Page
of 18
Search research articles
Search
Showing results (91-100 of 174) with videos related to
Sort By:
Page
of 18
Scientific Reports
|
November 17, 2017
Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency
Syeda T Ahmed, Charlotte L Alston, Sila Hopton, et al.
Journal of Rare Diseases (Berlin, Germany)
|
August 11, 2025
Severe clinical manifestation of mitochondrial disease due to the m.3243A>T variant: a case report of early-onset, multi-organ involvement and premature death
Hannah Gillespie, Yi Shiau Ng, Katrina M Wood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations
Helen R Griffin, Angela Pyle, Emma L Blakely, et al.
The Cancer Journal From Scientific American
|
March 1, 1996
The accumulation of multiple genetic abnormalities in individual tumor cells in human breast cancers: clinical prognostic implications
S E Shackney, A A Pollice, C A Smith, et al.
The Journal of Infectious Diseases
|
May 15, 2020
Hepatitis C Virus (HCV) Direct-Acting Antiviral Therapy in Persons With Human Immunodeficiency Virus-HCV Genotype 1 Coinfection Resulting in High Rate of Sustained Virologic Response and Variable in Normalization of Soluble Markers of Immune Activation
Donald D Anthony, Mark S Sulkowski, Laura M Smeaton, et al.
JAMA Neurology
|
April 26, 2016
Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
Mika H Martikainen, Yi Shiau Ng, Gráinne S Gorman, et al.
Antiviral Therapy
|
February 17, 2007
Safety and efficacy of extended-release niacin for the treatment of dyslipidaemia in patients with HIV infection: AIDS Clinical Trials Group Study A5148
Michael P Dubé, Julia W Wu, Judith A Aberg, et al.
AIDS Research and Human Retroviruses
|
October 13, 2005
A randomized trial of the efficacy and safety of fenofibrate versus pravastatin in HIV-infected subjects with lipid abnormalities: AIDS Clinical Trials Group Study 5087
Judith A Aberg, Robert A Zackin, Susan W Brobst, et al.
Neurogenetics
|
November 25, 2014
A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Michael J Keogh, D Daud, A Pyle, et al.
Biochimica Et Biophysica Acta
|
October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
Abdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Page
of 18