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Journal Abstract Search

159 related items for PubMed ID: 3706414

  • 21. Stereological analysis of peroxisomes and mitochondria in intestinal epithelium of patients with peroxisomal deficiency disorders: Zellweger's syndrome and neonatal-onset adrenoleukodystrophy.
    Black VH, Cornacchia L.
    Am J Anat; 1986 Sep; 177(1):107-18. PubMed ID: 3776884
    [Abstract] [Full Text] [Related]

  • 22. [A child with Zellweger's cerebrohepatorenal syndrome].
    Govaerts L, Corstiaensen J, Bakkeren J, Trujbels F, Monnens L.
    Tijdschr Kindergeneeskd; 1983 Apr; 51(2):65-7. PubMed ID: 6879587
    [Abstract] [Full Text] [Related]

  • 23. Clinical approach to inherited peroxisomal disorders: a series of 27 patients.
    Baumgartner MR, Poll-The BT, Verhoeven NM, Jakobs C, Espeel M, Roels F, Rabier D, Levade T, Rolland MO, Martinez M, Wanders RJ, Saudubray JM.
    Ann Neurol; 1998 Nov; 44(5):720-30. PubMed ID: 9818927
    [Abstract] [Full Text] [Related]

  • 24. [Neonatal adrenoleukodystrophy. Apropos of 3 cases in siblings].
    Sarda H, Henry V, Le Loc'h H, Aubourg P, Poll-The BT, Saudubray JM.
    Ann Pediatr (Paris); 1989 Apr; 36(4):233-6. PubMed ID: 2662877
    [Abstract] [Full Text] [Related]

  • 25. Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.
    Schutgens RB, Wanders RJ, Heymans HS, Schram AW, Tager JM, Schrakamp G, van den Bosch H.
    J Inherit Metab Dis; 1987 Apr; 10 Suppl 1():33-45. PubMed ID: 3119940
    [Abstract] [Full Text] [Related]

  • 26. Cerebrohepatorenal syndrome of Zellweger: a peroxisomal deficiency disorder. Case report and review.
    Kaplan M, Eidelman AI, Shapira Y, Collins J, Goldfischer S.
    Isr J Med Sci; 1988 Jun; 24(6):319-24. PubMed ID: 3042692
    [Abstract] [Full Text] [Related]

  • 27. Developmental delay and growth failure caused by a peroxisomal disorder, dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiency.
    Elias ER, Mobassaleh M, Hajra AK, Moser AB.
    Am J Med Genet; 1998 Nov 16; 80(3):223-6. PubMed ID: 9843043
    [Abstract] [Full Text] [Related]

  • 28. [Liver pathologies due to peroxisome disorders].
    Lovisetto P, Raviolo P.
    Recenti Prog Med; 1994 Feb 16; 85(2):134-41. PubMed ID: 8184191
    [Abstract] [Full Text] [Related]

  • 29. Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.
    Suzuki Y, Shimozawa N, Orii T, Igarashi N, Kono N, Matsui A, Inoue Y, Yokota S, Hashimoto T.
    J Pediatr; 1988 Nov 16; 113(5):841-5. PubMed ID: 3183838
    [Abstract] [Full Text] [Related]

  • 30. Neonatal adrenoleukodystrophy: a clinical, pathologic, and biochemical study.
    Farrell DF.
    Pediatr Neurol; 2012 Nov 16; 47(5):330-6. PubMed ID: 23044013
    [Abstract] [Full Text] [Related]

  • 31. [Treatment of generalized peroxisomal disorders with docosahexaenoic acid ethyl ether].
    Martínez M, Vázquez E, García-Silva MT, Beltrán JM, Castelló F, Pineda M, Mougan I.
    Rev Neurol; 1999 Jan 16; 28 Suppl 1():S59-64. PubMed ID: 10778491
    [Abstract] [Full Text] [Related]

  • 32. Peroxisomal disorders: clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families.
    Steinberg SJ, Elçioglu N, Slade CM, Sankaralingam A, Dennis N, Mohammed SN, Fensom AH.
    Am J Med Genet; 1999 Aug 27; 85(5):502-10. PubMed ID: 10405451
    [Abstract] [Full Text] [Related]

  • 33. Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy.
    Shimozawa N, Suzuki Y, Orii T, Yokota S, Hashimoto T.
    Pediatr Res; 1988 Dec 27; 24(6):723-7. PubMed ID: 3205629
    [Abstract] [Full Text] [Related]

  • 34. Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
    Kelley RI, Moser HW.
    Am J Med Genet; 1984 Dec 27; 19(4):791-5. PubMed ID: 6517102
    [Abstract] [Full Text] [Related]

  • 35. [Clinical symptoms of generalized peroxisomal disorders].
    Martínez M.
    Rev Neurol; 1999 Jan 27; 28 Suppl 1():S49-54. PubMed ID: 10778489
    [Abstract] [Full Text] [Related]

  • 36. Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.
    Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB.
    Eur J Pediatr; 1987 Sep 27; 146(5):477-83. PubMed ID: 2445576
    [Abstract] [Full Text] [Related]

  • 37. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.
    Brown FR, McAdams AJ, Cummins JW, Konkol R, Singh I, Moser AB, Moser HW.
    Johns Hopkins Med J; 1982 Dec 27; 151(6):344-51. PubMed ID: 7176294
    [No Abstract] [Full Text] [Related]

  • 38. Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.
    Schrakamp G, Schalkwijk CG, Schutgens RB, Wanders RJ, Tager JM, van den Bosch H.
    J Lipid Res; 1988 Mar 27; 29(3):325-34. PubMed ID: 3379344
    [Abstract] [Full Text] [Related]

  • 39. Plasmalogen deficiency in cultured skin fibroblasts from neonatal adrenoleukodystrophy.
    Sakai T, Antoku Y, Goto I.
    Exp Neurol; 1986 Oct 27; 94(1):149-54. PubMed ID: 3758277
    [Abstract] [Full Text] [Related]

  • 40. Glyceryl ethers in peroxisomal disease.
    Poulos A, Bankier A, Beckman K, Johnson D, Robertson EF, Sharp P, Sheffield L, Singh H, Usher S, Wise G.
    Clin Genet; 1991 Jan 27; 39(1):13-25. PubMed ID: 1705185
    [Abstract] [Full Text] [Related]

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