| Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease Z Li, S Yang, H Lin, J Huang, PA Watkins, AB Moser, C DeSimone, ... Hepatology 37 (2), 343-350, 2003 | 1272 | 2003 |
| Functions of plasmalogen lipids in health and disease NE Braverman, AB Moser Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (9 …, 2012 | 1067 | 2012 |
| Peroxisome biogenesis disorders SJ Steinberg, G Dodt, GV Raymond, NE Braverman, AB Moser, ... Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1763 (12), 1733-1748, 2006 | 596 | 2006 |
| X-linked adrenoleukodystrophy HW Moser, KD Smith, AB Moser NEUROLOGICAL DISEASE AND THERAPY, 377, 1995 | 575* | 1995 |
| Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata N Braverman, G Steel, C Obie, A Moser, H Moser, SJ Gould, D Valle Nature genetics 15 (4), 369-376, 1997 | 522 | 1997 |
| Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders G Dodt, N Braverman, C Wong, A Moser, HW Moser, P Watkins, D Valle, ... Nature genetics 9 (2), 115-125, 1995 | 509 | 1995 |
| Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids HW Moser, AB Moser, KK Frayer, W Chen, JD Schulman, BP O'Neill, ... Neurology 51 (2), 334-334-a, 1998 | 480 | 1998 |
| Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening L Bezman, AB Moser, GV Raymond, P Rinaldo, PA Watkins, KD Smith, ... Annals of neurology 49 (4), 512-517, 2001 | 420 | 2001 |
| Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls AB Moser, N Kreiter, L Bezman, SE Lu, GV Raymond, S Naidu, HW Moser Annals of Neurology: Official Journal of the American Neurological …, 1999 | 411 | 1999 |
| Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells. BR Migeon, HW Moser, AB Moser, J Axelman, D Sillence, RA Norum Proceedings of the National Academy of Sciences 78 (8), 5066-5070, 1981 | 336 | 1981 |
| A mouse model for X-linked adrenoleukodystrophy JF Lu, AM Lawler, PA Watkins, JM Powers, AB Moser, HW Moser, ... Proceedings of the National Academy of Sciences 94 (17), 9366-9371, 1997 | 308 | 1997 |
| Mutations in the gene encoding 3β-hydroxysteroid-Δ8, Δ7-isomerase cause X-linked dominant Conradi-Hünermann syndrome N Braverman, P Lin, FF Moebius, C Obie, A Moser, H Glossmann, ... Nature genetics 22 (3), 291-294, 1999 | 301 | 1999 |
| Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy S Kemp, HM Wei, JF Lu, LT Braiterman, MC McGuinness, AB Moser, ... Nature medicine 4 (11), 1261-1268, 1998 | 295 | 1998 |
| Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo’s oil HW Moser, GV Raymond, SE Lu, LR Muenz, AB Moser, J Xu, RO Jones, ... Archives of neurology 62 (7), 1073-1080, 2005 | 283 | 2005 |
| Adrenoleukodystrophy: phenotypic variability and implications for therapy HW Moser, AB Moser, KD Smith, A Bergin, J Borel, J Shankroff, OC Stine, ... Journal of inherited metabolic disease 15 (4), 645-664, 1992 | 279 | 1992 |
| The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implications JM Powers, Y Liu, AB Moser, HW Moser Journal of Neuropathology & Experimental Neurology 51 (6), 630-643, 1992 | 277 | 1992 |
| Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups AB Moser, M Rasmussen, S Naidu, PA Watkins, M McGuinness, AK Hajra, ... The Journal of pediatrics 127 (1), 13-22, 1995 | 265 | 1995 |
| Clinical and biochemical spectrum of patients with RSH/Smith‐Lemli‐Opitz syndrome and abnormal cholesterol metabolism C Cunniff, LE Kratz, A Moser, MR Natowicz, RI Kelley American journal of medical genetics 68 (3), 263-269, 1997 | 255 | 1997 |
| Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes RI Kelley, NS Datta, WB Dobyns, AK Hajra, AB Moser, MJ Noetzel, ... American journal of medical genetics 23 (4), 869-901, 1986 | 249 | 1986 |
| Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines NE Braverman, GV Raymond, WB Rizzo, AB Moser, ME Wilkinson, ... Molecular genetics and metabolism 117 (3), 313-321, 2016 | 240 | 2016 |
