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Neurology
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June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene
C M Sue, K Tanji, G Hadjigeorgiou, et al.
Journal of Viral Hepatitis
|
March 27, 2007
Peginterferon alpha-2b plus ribavirin vs interferon alpha-2b plus ribavirin for chronic hepatitis C in HIV-coinfected patients
M Crespo, S Sauleda, J I Esteban, et al.
Journal of Medical Genetics
|
January 7, 2009
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein
E López-Gallardo, A Solano, M D Herrero-Martín, et al.
Brain : a Journal of Neurology
|
July 26, 2013
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms
Celine Perier, Andreas Bender, Elena García-Arumí, et al.
European Journal of Applied Physiology
|
August 5, 2010
Excessive skeletal muscle recruitment during strenuous exercise in McArdle patients
Dale E Rae, Timothy D Noakes, Alejandro F San Juan, et al.
International Journal of Molecular Sciences
|
December 22, 2020
Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models
Aitana Almodóvar-Payá, Mónica Villarreal-Salazar, Noemí de Luna, et al.
Age (Dordrecht, Netherlands)
|
January 29, 2013
Association of the K153R polymorphism in the myostatin gene and extreme longevity
Nuria Garatachea, Tomàs Pinós, Yolanda Cámara, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 26, 2016
Taking advantage of an old concept, "illegitimate transcription", for a proposed novel method of genetic diagnosis of McArdle disease
Ines Garcia-Consuegra, Alberto Blázquez, Juan Carlos Rubio, et al.
Mitochondrion
|
August 23, 2011
Are mitochondrial haplogroups associated with elite athletic status? A study on a Spanish cohort
Gisela Nogales-Gadea, Tomàs Pinós, Jonatan R Ruiz, et al.
Journal of the Neurological Sciences
|
May 9, 2006
Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation
Rafael Artuch, Gloria Brea-Calvo, Paz Briones, et al.
Page
of 32
Search research articles
Search
Showing results (251-260 of 313) with videos related to
Sort By:
Page
of 32
Neurology
|
June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene
C M Sue, K Tanji, G Hadjigeorgiou, et al.
Journal of Viral Hepatitis
|
March 27, 2007
Peginterferon alpha-2b plus ribavirin vs interferon alpha-2b plus ribavirin for chronic hepatitis C in HIV-coinfected patients
M Crespo, S Sauleda, J I Esteban, et al.
Journal of Medical Genetics
|
January 7, 2009
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein
E López-Gallardo, A Solano, M D Herrero-Martín, et al.
Brain : a Journal of Neurology
|
July 26, 2013
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms
Celine Perier, Andreas Bender, Elena García-Arumí, et al.
European Journal of Applied Physiology
|
August 5, 2010
Excessive skeletal muscle recruitment during strenuous exercise in McArdle patients
Dale E Rae, Timothy D Noakes, Alejandro F San Juan, et al.
International Journal of Molecular Sciences
|
December 22, 2020
Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models
Aitana Almodóvar-Payá, Mónica Villarreal-Salazar, Noemí de Luna, et al.
Age (Dordrecht, Netherlands)
|
January 29, 2013
Association of the K153R polymorphism in the myostatin gene and extreme longevity
Nuria Garatachea, Tomàs Pinós, Yolanda Cámara, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 26, 2016
Taking advantage of an old concept, "illegitimate transcription", for a proposed novel method of genetic diagnosis of McArdle disease
Ines Garcia-Consuegra, Alberto Blázquez, Juan Carlos Rubio, et al.
Mitochondrion
|
August 23, 2011
Are mitochondrial haplogroups associated with elite athletic status? A study on a Spanish cohort
Gisela Nogales-Gadea, Tomàs Pinós, Jonatan R Ruiz, et al.
Journal of the Neurological Sciences
|
May 9, 2006
Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation
Rafael Artuch, Gloria Brea-Calvo, Paz Briones, et al.
Page
of 32