Moser HW - Search Results

1

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.

Kelley RI, Datta NS, Dobyns WB, Hajra AK, Moser AB, Noetzel MJ, Zackai EH, Moser HW. Kelley RI, et al. Among authors: moser hw, moser ab. Am J Med Genet. 1986 Apr;23(4):869-901. doi: 10.1002/ajmg.1320230404. Am J Med Genet. 1986. PMID: 3515938 Review.

2

Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.

Kelley RI, Moser HW. Kelley RI, et al. Among authors: moser hw. Am J Med Genet. 1984 Dec;19(4):791-5. doi: 10.1002/ajmg.1320190420. Am J Med Genet. 1984. PMID: 6517102

3

Adrenoleukodystrophy and Zellweger syndrome.

Moser HW, Moser AB, Chen WW, Watkins PA. Moser HW, et al. Among authors: moser ab. Prog Clin Biol Res. 1990;321:511-35. Prog Clin Biol Res. 1990. PMID: 2183241 Review. No abstract available.

4

Myopathy in an infant with a fatal peroxisomal disorder.

Wolff J, Nyhan WL, Powell H, Takahashi D, Hutzler J, Hajra AK, Datta NS, Singh I, Moser HW. Wolff J, et al. Among authors: moser hw. Pediatr Neurol. 1986 May-Jun;2(3):141-6. doi: 10.1016/0887-8994(86)90004-4. Pediatr Neurol. 1986. PMID: 3508688 Free article.

5

Urinary bile acids and peroxisomal bifunctional enzyme deficiency.

Natowicz MR, Evans JE, Kelley RI, Moser AB, Watkins PA, Moser HW. Natowicz MR, et al. Among authors: moser hw, moser ab. Am J Med Genet. 1996 May 17;63(2):356-62. doi: 10.1002/(SICI)1096-8628(19960517)63:2<356::AID-AJMG6>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8725785

6

A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patients.

Moser AB, Borel J, Odone A, Naidu S, Cornblath D, Sanders DB, Moser HW. Moser AB, et al. Among authors: moser hw. Ann Neurol. 1987 Mar;21(3):240-9. doi: 10.1002/ana.410210305. Ann Neurol. 1987. PMID: 2440378

7

Adrenoleukodystrophy carrier state presenting as a chronic nonprogressive spinal cord disorder.

Noetzel MJ, Landau WM, Moser HW. Noetzel MJ, et al. Among authors: moser hw. Arch Neurol. 1987 May;44(5):566-7. doi: 10.1001/archneur.1987.00520170092031. Arch Neurol. 1987. PMID: 3579671

8

Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome.

Powers JM, Tummons RC, Moser AB, Moser HW, Huff DS, Kelley RI. Powers JM, et al. Among authors: moser hw, moser ab. Acta Neuropathol. 1987;73(4):333-43. doi: 10.1007/BF00688256. Acta Neuropathol. 1987. PMID: 3618126

9

Pathologic findings in adrenoleukodystrophy heterozygotes.

Powers JM, Moser HW, Moser AB, Ma CK, Elias SB, Norum RA. Powers JM, et al. Among authors: moser hw, moser ab. Arch Pathol Lab Med. 1987 Feb;111(2):151-3. Arch Pathol Lab Med. 1987. PMID: 3813829

10

Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.

Wanders RJ, Schutgens RB, Schrakamp G, Tager JM, Van den Bosch H, Moser AB, Moser HW. Wanders RJ, et al. Among authors: moser hw, moser ab. J Neurol Sci. 1987 Feb;77(2-3):331-40. doi: 10.1016/0022-510x(87)90132-8. J Neurol Sci. 1987. PMID: 3819771

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