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N J Manning

Showing results (41-50 of 48) with videos related to

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Annals of Clinical Biochemistry|March 1, 1994
Quality assessment of urinary organic acid analysisJ R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, F Allison, G W Lowther, et al.
Antimicrobial Agents and Chemotherapy|June 1, 1997
Itraconazole resistance in Aspergillus fumigatusD W Denning, K Venkateswarlu, K L Oakley, et al.
Prenatal Diagnosis|June 1, 1994
Prenatal diagnosis of glutathione synthase deficiencyN J Manning, N P Davies, S E Olpin, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Annals of Clinical Biochemistry|March 1, 1994
Quality assessment of urinary organic acid analysisJ R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, F Allison, G W Lowther, et al.
Antimicrobial Agents and Chemotherapy|June 1, 1997
Itraconazole resistance in Aspergillus fumigatusD W Denning, K Venkateswarlu, K L Oakley, et al.
Prenatal Diagnosis|June 1, 1994
Prenatal diagnosis of glutathione synthase deficiencyN J Manning, N P Davies, S E Olpin, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Pageof 5