Watkins PA - Search Results

1

Cerebral X-linked adrenoleukodystrophy in a girl with Xq27-Ter deletion.

Hershkovitz E, Narkis G, Shorer Z, Moser AB, Watkins PA, Moser HW, Manor E. Hershkovitz E, et al. Among authors: watkins pa. Ann Neurol. 2002 Aug;52(2):234-7. doi: 10.1002/ana.10248. Ann Neurol. 2002. PMID: 12210797

2

Adrenoleukodystrophy and Zellweger syndrome.

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

3

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids.

McGuinness MC, Moser AB, Moser HW, Watkins PA. McGuinness MC, et al. Among authors: watkins pa. Biochem Biophys Res Commun. 1990 Oct 15;172(1):364-9. doi: 10.1016/s0006-291x(05)80218-9. Biochem Biophys Res Commun. 1990. PMID: 2222480 Free article.

4

Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates.

Moser HW, Mihalik SJ, Watkins PA. Moser HW, et al. Among authors: watkins pa. Brain Dev. 1989;11(2):80-90. doi: 10.1016/s0387-7604(89)80074-9. Brain Dev. 1989. PMID: 2653074 Free article. Review.

5

Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment.

Watkins PA, Naidu S, Moser HW. Watkins PA, et al. J Inherit Metab Dis. 1987;10 Suppl 1:46-53. doi: 10.1007/BF01812846. J Inherit Metab Dis. 1987. PMID: 3119941 Review.

6

Prenatal diagnosis of rhizomelic chondrodysplasia punctata.

Hoefler S, Hoefler G, Moser AB, Watkins PA, Chen WW, Moser HW. Hoefler S, et al. Among authors: watkins pa. Prenat Diagn. 1988 Oct;8(8):571-6. doi: 10.1002/pd.1970080804. Prenat Diagn. 1988. PMID: 3205862

7

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.

Naidu S, Hoefler G, Watkins PA, Chen WW, Moser AB, Hoefler S, Rance NE, Powers JM, Beard M, Green WR, et al. Naidu S, et al. Among authors: watkins pa. Neurology. 1988 Jul;38(7):1100-7. doi: 10.1212/wnl.38.7.1100. Neurology. 1988. PMID: 3386829

8

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

Chen WW, Watkins PA, Osumi T, Hashimoto T, Moser HW. Chen WW, et al. Among authors: watkins pa. Proc Natl Acad Sci U S A. 1987 Mar;84(5):1425-8. doi: 10.1073/pnas.84.5.1425. Proc Natl Acad Sci U S A. 1987. PMID: 3469675 Free PMC article.

9

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Watkins PA, Gould SJ, Smith MA, Braiterman LT, Wei HM, Kok F, Moser AB, Moser HW, Smith KD. Watkins PA, et al. Am J Hum Genet. 1995 Aug;57(2):292-301. Am J Hum Genet. 1995. PMID: 7668254 Free PMC article.

10

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies.

Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW. Watkins PA, et al. Ann Neurol. 1995 Sep;38(3):472-7. doi: 10.1002/ana.410380322. Ann Neurol. 1995. PMID: 7668838

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