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Neurobiology of Disease
|
September 25, 2002
Beta-amyloid fragment 25-35 causes mitochondrial dysfunction in primary cortical neurons
C S Casley, J M Land, M A Sharpe, et al.
Biochemical Society Transactions
|
October 10, 1998
Stimulation of glyceraldehyde-3-phosphate dehydrogenase by oxyhemoglobin
P S Brookes, J Haley, P Cutler, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
January 15, 2000
Neonatal hypoglycaemia in Nepal 1. Prevalence and risk factors
D K Pal, D S Manandhar, S Rajbhandari, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
January 15, 2000
Neonatal hypoglycaemia in Nepal 2. Availability of alternative fuels
A M de L Costello, D K Pal, D S Manandhar, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia
I P Hargreaves, S J R Heales, A Briddon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1995
Evidence for increased nitric oxide production in multiple sclerosis
A W Johnson, J M Land, E J Thompson, et al.
Annals of Clinical Biochemistry
|
January 1, 1996
Age dependent changes in the cerebrospinal fluid concentration of nitrite and nitrate
J D Clelland, M P Brand, J P Bolaños, et al.
Journal of Neurochemistry
|
June 1, 1997
Nitric oxide-mediated mitochondrial damage in the brain: mechanisms and implications for neurodegenerative diseases
J P Bolaños, A Almeida, V Stewart, et al.
Biochimica Et Biophysica Acta
|
March 17, 1999
Nitric oxide, mitochondria and neurological disease
S J Heales, J P Bolaños, V C Stewart, et al.
Journal of Inherited Metabolic Disease
|
May 15, 2002
Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion
P Hargreaves, S Rahman, P Guthrie, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 83) with videos related to
Sort By:
Page
of 9
Neurobiology of Disease
|
September 25, 2002
Beta-amyloid fragment 25-35 causes mitochondrial dysfunction in primary cortical neurons
C S Casley, J M Land, M A Sharpe, et al.
Biochemical Society Transactions
|
October 10, 1998
Stimulation of glyceraldehyde-3-phosphate dehydrogenase by oxyhemoglobin
P S Brookes, J Haley, P Cutler, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
January 15, 2000
Neonatal hypoglycaemia in Nepal 1. Prevalence and risk factors
D K Pal, D S Manandhar, S Rajbhandari, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
January 15, 2000
Neonatal hypoglycaemia in Nepal 2. Availability of alternative fuels
A M de L Costello, D K Pal, D S Manandhar, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia
I P Hargreaves, S J R Heales, A Briddon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1995
Evidence for increased nitric oxide production in multiple sclerosis
A W Johnson, J M Land, E J Thompson, et al.
Annals of Clinical Biochemistry
|
January 1, 1996
Age dependent changes in the cerebrospinal fluid concentration of nitrite and nitrate
J D Clelland, M P Brand, J P Bolaños, et al.
Journal of Neurochemistry
|
June 1, 1997
Nitric oxide-mediated mitochondrial damage in the brain: mechanisms and implications for neurodegenerative diseases
J P Bolaños, A Almeida, V Stewart, et al.
Biochimica Et Biophysica Acta
|
March 17, 1999
Nitric oxide, mitochondria and neurological disease
S J Heales, J P Bolaños, V C Stewart, et al.
Journal of Inherited Metabolic Disease
|
May 15, 2002
Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion
P Hargreaves, S Rahman, P Guthrie, et al.
Page
of 9