Nerve conduction studies in adrenomyeloneuropathy.

Por Chaudhry, V, Moser, H W, Cornblath, D R
Publicado em 1996

Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.

Por Singh, I, Moser, A E, Goldfischer, S, Moser, H W
Publicado em 1984

Frequent alterations of visual pigment genes in adrenoleukodystrophy.

Por Aubourg, P R, Sack, G H, Moser, H W
Publicado em 1988

Color vision defects in adrenomyeloneuropathy.

Por Sack, G H, Raven, M B, Moser, H W
Publicado em 1989

Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and females.

Por Jaffe, R., Crumrine, P., Hashida, Y., Moser, H. W.
Publicado em 1982

Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.

Por Hoefler, G, Paschke, E, Hoefler, S, Moser, A B, Moser, H W
Publicado em 1991

Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.

Por Chen, W W, Watkins, P A, Osumi, T, Hashimoto, T, Moser, H W
Publicado em 1987

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

Por Warren, D S, Morrell, J C, Moser, H W, Valle, D, Gould, S J
Publicado em 1998

Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.

Por Shimozawa, N, Suzuki, Y, Orii, T, Moser, A, Moser, H W, Wanders, R J
Publicado em 1993

Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color vision.

Por Alpern, M, Sack, G H, Krantz, D H, Jenness, J, Zhang, H, Moser, H W
Publicado em 1993

Low-density particles (W-particles) containing catalase in Zellweger syndrome and normal fibroblasts.

Por Aikawa, J, Chen, W W, Kelley, R I, Tada, K, Moser, H W, Chen, G L
Publicado em 1991

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

Por Migeon, B R, Moser, H W, Moser, A B, Axelman, J, Sillence, D, Norum, R A
Publicado em 1981

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

Por Yahraus, T, Braverman, N, Dodt, G, Kalish, J E, Morrell, J C, Moser, H W, Valle, D, Gould, S J
Publicado em 1996

Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Por Sack, G H, Alpern, M, Webster, T, Feil, R P, Morrell, J C, Chen, G, Chen, W, Caskey, C T, Moser, H W
Publicado em 1993

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Por Watkins, P A, Gould, S J, Smith, M A, Braiterman, L T, Wei, H M, Kok, F, Moser, A B, Moser, H W, Smith, K D
Publicado em 1995

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis.

Por van Grunsven, E G, van Berkel, E, Mooijer, P A, Watkins, P A, Moser, H W, Suzuki, Y, Jiang, L L, Hashimoto, T, Hoefler, G, Adamski, J, Wanders, R J
Publicado em 1999