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Nature Reviews. Disease Primers
|
October 25, 2016
Mitochondrial diseases
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Optics Letters
|
September 29, 2017
Tunable mid-infrared source of light carrying orbital angular momentum in the femtosecond regime
Antoine Camper, Hyunwook Park, Yu Hang Lai, et al.
Cell
|
August 12, 1988
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface
E Bonilla, C E Samitt, A F Miranda, et al.
Therapeutic Advances in Rare Disease
|
March 6, 2024
A United States-based patient-reported adult polyglucosan body disease registry: initial results
Jacy Sparks, Francesco Michelassi, John L P Thompson, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
C T Moraes, F Ciacci, E Bonilla, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 12, 2021
Sex-based differences after a single bout of exercise on PGC1α isoforms in skeletal muscle: A pilot study
Daniela D'Amico, Antonella Marino Gammazza, Filippo Macaluso, et al.
The American Journal of Nursing
|
March 23, 2023
Affirmative Palliative Care for Transgender and Gender Nonconforming Individuals
Megan Pfitzinger Lippe, Joshua C Eyer, Kailey E Roberts, et al.
Structural Dynamics (Melville, N.Y.)
|
July 26, 2019
High-harmonic spectroscopy of transient two-center interference calculated with time-dependent density-functional theory
François Mauger, Paul M Abanador, Timothy D Scarborough, et al.
Journal of Child Neurology
|
October 18, 2005
Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutations
Stacey K H Tay, Sabrina Sacconi, H Ohran Akman, et al.
Placenta
|
February 22, 2008
Placental involvement in glycogen storage disease type IV
A E Konstantinidou, H Anninos, S Dertinger, et al.
Page
of 95
Search research articles
Search
Showing results (701-710 of 942) with videos related to
Sort By:
Page
of 95
Nature Reviews. Disease Primers
|
October 25, 2016
Mitochondrial diseases
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Optics Letters
|
September 29, 2017
Tunable mid-infrared source of light carrying orbital angular momentum in the femtosecond regime
Antoine Camper, Hyunwook Park, Yu Hang Lai, et al.
Cell
|
August 12, 1988
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface
E Bonilla, C E Samitt, A F Miranda, et al.
Therapeutic Advances in Rare Disease
|
March 6, 2024
A United States-based patient-reported adult polyglucosan body disease registry: initial results
Jacy Sparks, Francesco Michelassi, John L P Thompson, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
C T Moraes, F Ciacci, E Bonilla, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 12, 2021
Sex-based differences after a single bout of exercise on PGC1α isoforms in skeletal muscle: A pilot study
Daniela D'Amico, Antonella Marino Gammazza, Filippo Macaluso, et al.
The American Journal of Nursing
|
March 23, 2023
Affirmative Palliative Care for Transgender and Gender Nonconforming Individuals
Megan Pfitzinger Lippe, Joshua C Eyer, Kailey E Roberts, et al.
Structural Dynamics (Melville, N.Y.)
|
July 26, 2019
High-harmonic spectroscopy of transient two-center interference calculated with time-dependent density-functional theory
François Mauger, Paul M Abanador, Timothy D Scarborough, et al.
Journal of Child Neurology
|
October 18, 2005
Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutations
Stacey K H Tay, Sabrina Sacconi, H Ohran Akman, et al.
Placenta
|
February 22, 2008
Placental involvement in glycogen storage disease type IV
A E Konstantinidou, H Anninos, S Dertinger, et al.
Page
of 95