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Ecotoxicology and Environmental Safety
|
December 1, 2020
Relationship of arsenic and chromium availability with carbon functional groups, aluminum and iron in Little Washita River Experimental Watershed Reservoirs, Oklahoma, USA
L W Ngatia, L M De Oliveira, O C Betiku, et al.
Journal of Medical Genetics
|
October 7, 2004
Mutations of the mitochondrial ND1 gene as a cause of MELAS
D M Kirby, R McFarland, A Ohtake, et al.
Critical Care Medicine
|
January 15, 1998
Effects of inhaled nitric oxide in patients with acute respiratory distress syndrome: results of a randomized phase II trial. Inhaled Nitric Oxide in ARDS Study Group
R P Dellinger, J L Zimmerman, R W Taylor, et al.
Neurology
|
February 11, 2009
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
R G Whittaker, J K Blackwood, C L Alston, et al.
The International Journal of Behavioral Nutrition and Physical Activity
|
June 8, 2024
Correction: Validation of actigraphy sleep metrics in children aged 8 to 16 years: considerations for device type, placement and algorithms
K A Meredith-Jones, J J Haszard, A Graham-DeMello, et al.
Neurology
|
May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
G Hudson, M Deschauer, R W Taylor, et al.
The International Journal of Behavioral Nutrition and Physical Activity
|
April 16, 2024
Validation of actigraphy sleep metrics in children aged 8 to 16 years: considerations for device type, placement and algorithms
K A Meredith-Jones, J J Haszard, A Graham-DeMello, et al.
Annals of Neurology
|
August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutations
P F Chinnery, M A Johnson, T M Wardell, et al.
Biochimica Et Biophysica Acta
|
October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness
D Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain
A A Morris, R W Taylor, M A Birch-Machin, et al.
Page
of 26
Search research articles
Search
Showing results (221-230 of 254) with videos related to
Sort By:
Page
of 26
Ecotoxicology and Environmental Safety
|
December 1, 2020
Relationship of arsenic and chromium availability with carbon functional groups, aluminum and iron in Little Washita River Experimental Watershed Reservoirs, Oklahoma, USA
L W Ngatia, L M De Oliveira, O C Betiku, et al.
Journal of Medical Genetics
|
October 7, 2004
Mutations of the mitochondrial ND1 gene as a cause of MELAS
D M Kirby, R McFarland, A Ohtake, et al.
Critical Care Medicine
|
January 15, 1998
Effects of inhaled nitric oxide in patients with acute respiratory distress syndrome: results of a randomized phase II trial. Inhaled Nitric Oxide in ARDS Study Group
R P Dellinger, J L Zimmerman, R W Taylor, et al.
Neurology
|
February 11, 2009
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
R G Whittaker, J K Blackwood, C L Alston, et al.
The International Journal of Behavioral Nutrition and Physical Activity
|
June 8, 2024
Correction: Validation of actigraphy sleep metrics in children aged 8 to 16 years: considerations for device type, placement and algorithms
K A Meredith-Jones, J J Haszard, A Graham-DeMello, et al.
Neurology
|
May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
G Hudson, M Deschauer, R W Taylor, et al.
The International Journal of Behavioral Nutrition and Physical Activity
|
April 16, 2024
Validation of actigraphy sleep metrics in children aged 8 to 16 years: considerations for device type, placement and algorithms
K A Meredith-Jones, J J Haszard, A Graham-DeMello, et al.
Annals of Neurology
|
August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutations
P F Chinnery, M A Johnson, T M Wardell, et al.
Biochimica Et Biophysica Acta
|
October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness
D Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain
A A Morris, R W Taylor, M A Birch-Machin, et al.
Page
of 26