H. W. Moser

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Barbara R. Migeon, H. W. Moser, Ann B. Moser et al. · Proceedings of the National Academy of Sciences · 1981 · 291 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy

Daniel J. Loes, Ali Fatemi, Elias R. Melhem et al. · Neurology · 2003 · 270 citations

Public Health, Child Health, Pediatrics +13

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

T. Yahraus, Nancy Braverman, Gabriele Dodt et al. · The EMBO Journal · 1996 · 187 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +10

MR findings in adult-onset adrenoleukodystrophy.

Ashok Kumar, Wolfgang Köhler, B. Kruse et al. · PubMed · 1995 · 133 citations · Full text

Medicine, Neurology, Neuroscience +17

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Paul A. Watkins, Stephen J. Gould, Marilyn A. Smith et al. · PubMed · 1995 · 129 citations

Medicine, Molecular Medicine, Pathology +3