Moser A - Search Results

1

Diagnosis and follow-up of a case of peroxisomal disorder with peroxisomal mosaicism.

Pineda M, Girós M, Roels F, Espeel M, Ruiz M, Moser A, Moser HW, Wanders RJ, Pavia C, Conill J, Aracil A, Amat L, Pampols T. Pineda M, et al. Among authors: moser hw, moser a. J Child Neurol. 1999 Jul;14(7):434-9. doi: 10.1177/088307389901400705. J Child Neurol. 1999. PMID: 10573465

2

Very long-chain fatty acids in diagnosis, pathogenesis, and therapy of peroxisomal disorders.

Moser HW, Moser AB. Moser HW, et al. Among authors: moser ab. Lipids. 1996 Mar;31 Suppl:S141-4. doi: 10.1007/BF02637066. Lipids. 1996. PMID: 8729109 Review.

3

Peroxisomal disorders: overview.

Moser HW, Moser AB. Moser HW, et al. Among authors: moser ab. Ann N Y Acad Sci. 1996 Dec 27;804:427-41. doi: 10.1111/j.1749-6632.1996.tb18634.x. Ann N Y Acad Sci. 1996. PMID: 8993562 Review. No abstract available.

4

Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy study.

Santos MJ, Henderson SC, Moser AB, Moser HW, Lazarow PB. Santos MJ, et al. Among authors: moser hw, moser ab. Biol Cell. 2000 Apr;92(2):85-94. doi: 10.1016/s0248-4900(00)89016-4. Biol Cell. 2000. PMID: 10879629

5

Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis.

Su HM, Moser AB, Moser HW, Watkins PA. Su HM, et al. Among authors: moser hw, moser ab. J Biol Chem. 2001 Oct 12;276(41):38115-20. doi: 10.1074/jbc.M106326200. Epub 2001 Aug 10. J Biol Chem. 2001. PMID: 11500517 Free article.

6

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

Shimozawa N, Suzuki Y, Orii T, Moser A, Moser HW, Wanders RJ. Shimozawa N, et al. Among authors: moser hw, moser a. Am J Hum Genet. 1993 Apr;52(4):843-4. Am J Hum Genet. 1993. PMID: 7681622 Free PMC article. No abstract available.

7

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

Matsumoto N, Tamura S, Moser A, Moser HW, Braverman N, Suzuki Y, Shimozawa N, Kondo N, Fujiki Y. Matsumoto N, et al. Among authors: moser hw, moser a. J Hum Genet. 2001;46(5):273-7. doi: 10.1007/s100380170078. J Hum Genet. 2001. PMID: 11355018

8

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: moser hw, moser ab. 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.

9

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.

Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ. Slawecki ML, et al. Among authors: moser hw, moser ab. J Cell Sci. 1995 May;108 ( Pt 5):1817-29. doi: 10.1242/jcs.108.5.1817. J Cell Sci. 1995. PMID: 7544797

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. Among authors: moser hw, moser ab. Ann Neurol. 1995 Sep;38(3):472-7. doi: 10.1002/ana.410380322. Ann Neurol. 1995. PMID: 7668838

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