| Mammalian mitochondrial β-oxidation S EATON, KB BARTLETT, M POURFARZAM Biochemical Journal 320 (2), 345-357, 1996 | 598 | 1996 |
| Clear correlation of genotype with disease phenotype in very–long-chain Acyl-CoA dehydrogenase deficiency BS Andresen, S Olpin, BJHM Poorthuis, HR Scholte, C Vianey-Saban, ... The American Journal of Human Genetics 64 (2), 479-494, 1999 | 349 | 1999 |
| ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency RKJ Olsen, SE Olpin, BS Andresen, ZH Miedzybrodzka, M Pourfarzam, ... Brain 130 (8), 2045-2054, 2007 | 346 | 2007 |
| Combined enzyme defect of mitochondrial fatty acid oxidation. S Jackson, RS Kler, K Bartlett, H Briggs, LA Bindoff, M Pourfarzam, ... The Journal of clinical investigation 90 (4), 1219-1225, 1992 | 148 | 1992 |
| Are antioxidants helpful for disease prevention? V Hajhashemi, G Vaseghi, M Pourfarzam, A Abdollahi Research in pharmaceutical sciences 5 (1), 1, 2010 | 138 | 2010 |
| Very long‐chain acyl coenzyme A dehydrogenase deficiency presenting with exercise‐induced myoglobinuria I Ogilvie, M Pourfarzam, S Jackson, C Stockdale, K Bartlett, DM Turnbull Neurology 44 (3_part_1), 467-467, 1994 | 120 | 1994 |
| The mitochondrial trifunctional protein: centre of a β-oxidation metabolon? S Eaton, T Bursby, B Middleton, M Pourfarzam, K Mills, AW Johnson, ... Biochemical Society Transactions 28 (2), 177-182, 2000 | 110 | 2000 |
| Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation. RS Kler, S Jackson, K Bartlett, LA Bindoff, S Eaton, M Pourfarzam, ... Journal of Biological Chemistry 266 (34), 22932-22938, 1991 | 104 | 1991 |
| Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency M Pourfarzam, A Morris, M Appleton, A Craft, K Bartlett The Lancet 358 (9287), 1063-1064, 2001 | 103 | 2001 |
| Newborn screening for inherited metabolic disorders; news and views M Pourfarzam, F Zadhoush Journal of research in medical sciences: the official journal of Isfahan …, 2013 | 100 | 2013 |
| Synthesis and tyrosinase inhibitory properties of some novel derivatives of kojic acid L Saghaie, M Pourfarzam, A Fassihi, B Sartippour Research in pharmaceutical sciences 8 (4), 233, 2013 | 99 | 2013 |
| Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency SE Olpin, S Clark, BS Andresen, C Bischoff, RKJ Olsen, N Gregersen, ... Journal of inherited metabolic disease 28 (4), 533-544, 2005 | 83 | 2005 |
| Mitochondrial fatty acid β-oxidation in the retinal pigment epithelium T Tyni, M Johnson, S Eaton, M Pourfarzam, R Andrews, DM Turnbull Pediatric research 52 (4), 595-600, 2002 | 70 | 2002 |
| Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group B Merinero, B Perez, C Pérez‐Cerdá, A Rincon, LR Desviat, MA Martinez, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2008 | 69 | 2008 |
| Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency SE Olpin, A Afifi, S Clark, NJ Manning, JR Bonham, A Dalton, JV Leonard, ... Journal of inherited metabolic disease 26, 543-557, 2003 | 69 | 2003 |
| Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen S Kölker, GF Hoffmann, DSM Schor, P Feyh, L Wagner, I Jeffrey, ... Neuropediatrics 34 (05), 253-260, 2003 | 61 | 2003 |
| A review of strategies for untargeted urinary metabolomic analysis using gas chromatography–mass spectrometry M Khodadadi, M Pourfarzam Metabolomics 16, 1-14, 2020 | 51 | 2020 |
| Lipid‐storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late‐onset multiple acyl‐CoA dehydrogenation deficiency RKJ Olsen, M Pourfarzam, AAM Morris, RC Dias, I Knudsen, BS Andresen, ... Journal of inherited metabolic disease 27 (5), 671-678, 2004 | 51 | 2004 |
| Analysis of fatty acid oxidation intermediates in cultured fibroblasts to detect mitochondrial oxidation disorders M Pourfarzam, J Schaefer, DM Turnbull, K Bartlett Clinical chemistry 40 (12), 2267-2275, 1994 | 51 | 1994 |
| Associations between high density lipoprotein mean particle size and serum paraoxonase-1 activity AE Razavi, M Ani, M Pourfarzam, GA Naderi Journal of research in medical sciences: the official journal of Isfahan …, 2012 | 50 | 2012 |
