Synthesis and tyrosinase inhibitory properties of some novel derivatives of kojic acid
Saghaie, L, Pourfarzam, M, Fassihi, A, Sartippour, B
Published in Research in pharmaceutical sciences (01.10.2013)
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Published in Research in pharmaceutical sciences (01.10.2013)
Journal Article
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
Olsen, Rikke K. J., Olpin, Simon E., Andresen, Brage S., Miedzybrodzka, Zofia H., Pourfarzam, Morteza, Merinero, Begoña, Frerman, Frank E., Beresford, Michael W., Dean, John C. S., Cornelius, Nanna, Andersen, Oluf, Oldfors, Anders, Holme, Elisabeth, Gregersen, Niels, Turnbull, Douglass M., Morris, Andrew A. M.
Published in Brain (London, England : 1878) (01.08.2007)
Published in Brain (London, England : 1878) (01.08.2007)
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Journal Article
Are antioxidants helpful for disease prevention?
Hajhashemi, V, Vaseghi, G, Pourfarzam, M, Abdollahi, A
Published in Research in pharmaceutical sciences (01.01.2010)
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Published in Research in pharmaceutical sciences (01.01.2010)
Journal Article
Methylmalonic acidaemia: Examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group
Merinero, B., Pérez, B., Pérez-Cerdá, C., Rincón, A., Desviat, L. R., Martínez, M. A., Sala, P. Ruiz, García, M. J., Aldamiz-Echevarría, L., Campos, J., Cornejo, V., del Toro, M., Mahfoud, A., Martínez-Pardo, M., Parini, R., Pedrón, C., Peña-Quintana, L., Pérez, M., Pourfarzam, M., Ugarte, M.
Published in Journal of inherited metabolic disease (01.02.2008)
Published in Journal of inherited metabolic disease (01.02.2008)
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Journal Article
Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency
Pourfarzam, Morteza, Morris, Andrew, Appleton, Marie, Craft, Alan, Bartlett, Kim
Published in The Lancet (British edition) (29.09.2001)
Published in The Lancet (British edition) (29.09.2001)
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Journal Article
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency
Olpin, S. E., Clark, S., Andresen, B. S., Bischoff, C., Olsen, R. K. J., Gregersen, N., Chakrapani, A., Downing, M., Manning, N. J., Sharrard, M., Bonham, J. R., Muntoni, F., Turnbull, D. N., Pourfarzam, M.
Published in Journal of inherited metabolic disease (01.08.2005)
Published in Journal of inherited metabolic disease (01.08.2005)
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Journal Article
Plasma free and total carnitine measured in children by tandem mass spectrometry
Osorio, J H, Pourfarzam, M
Published in Brazilian journal of medical and biological research (01.11.2002)
Published in Brazilian journal of medical and biological research (01.11.2002)
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Journal Article
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency
Olpin, S. E., Afifi, A., Clark, S., Manning, N. J., Bonham, J. R., Dalton, A., Leonard, J. V., Land, J. M., Andresen, B. S., Morris, A. A., Muntoni, F., Turnbull, D., Pourfarzam, M., Rahman, S., Pollitt, R. J.
Published in Journal of inherited metabolic disease (01.01.2003)
Published in Journal of inherited metabolic disease (01.01.2003)
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Journal Article
The mitochondrial trifunctional protein: centre of a beta-oxidation metabolon?
Eaton, S, Bursby, T, Middleton, B, Pourfarzam, M, Mills, K, Johnson, A W, Bartlett, K
Published in Biochemical Society transactions (01.02.2000)
Published in Biochemical Society transactions (01.02.2000)
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Journal Article
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen
Kölker, S, Hoffmann, G F, Schor, D S M, Feyh, P, Wagner, L, Jeffrey, I, Pourfarzam, M, Okun, J G, Zschocke, J, Baric, I, Bain, M D, Jakobs, C, Chalmers, R A
Published in Neuropediatrics (01.10.2003)
Published in Neuropediatrics (01.10.2003)
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Journal Article
Lipid‐storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late‐onset multiple acyl‐CoA dehydrogenation deficiency
Olsen, R. K. J., Pourfarzam, M., Morris, A. A. M., Dias, R. C., Knudsen, I., Andresen, B. S., Gregersen, N., Olpin, S. E.
Published in Journal of inherited metabolic disease (01.01.2004)
Published in Journal of inherited metabolic disease (01.01.2004)
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Journal Article
Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria
Ogilvie, I, Pourfarzam, M, Jackson, S, Stockdale, C, Bartlett, K, Turnbull, D M
Published in Neurology (01.03.1994)
Published in Neurology (01.03.1994)
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Journal Article
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation
Kler, R S, Jackson, S, Bartlett, K, Bindoff, L A, Eaton, S, Pourfarzam, M, Frerman, F E, Goodman, S I, Watmough, N J, Turnbull, D M
Published in The Journal of biological chemistry (05.12.1991)
Published in The Journal of biological chemistry (05.12.1991)
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Journal Article
Combined enzyme defect of mitochondrial fatty acid oxidation
JACKSON, S, RAJINDER SINGH KLER, BARTLETT, K, BRIGGS, H, BINDOFF, L. A, POURFARZAM, M, GARDNER-MEDWIN, D, TURNBULL, D. M
Published in The Journal of clinical investigation (01.10.1992)
Published in The Journal of clinical investigation (01.10.1992)
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Journal Article
Determinación de valores normales de acilcarnitinas en una población infantil sana como herramienta diagnóstica de errores hereditarios de la β-oxidación mitocondrial de los ácidos grasos
Osorio, J.H., Pourfarzam, M.
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.12.2007)
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.12.2007)
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Journal Article
Decreased Na+/K+-ATPase Activity and Altered Susceptibility to Peroxidation and Lipid Composition in the Erythrocytes of Metabolic Syndrome Patients with Coronary Artery Disease
Namazi, Gholamreza, Asa, Parastoo, Sarrafzadegan, Nizal, Pourfarzam, Morteza
Published in Annals of nutrition and metabolism (01.01.2019)
Published in Annals of nutrition and metabolism (01.01.2019)
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