Hugo W. Moser

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

X-linked adrenoleukodystrophy

Imaging cortical association tracts in the human brain using diffusion‐tensor‐based axonal tracking

Peroxisome biogenesis disorders

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

Adrenoleukodystrophy

Cerebral X-linked adrenoleukodystrophy: the international hematopoietic cell transplantation experience from 1982 to 1999

Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

A mouse model for X-linked adrenoleukodystrophy

The Inflammatory Myelinopathy of Adreno-Leukodystrophy