These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

167 related items for PubMed ID: 7685190

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Clinical and biochemical characteristics of peroxisomal disorders: an update.
    Wanders RJ, Barth PG, Schutgens RB, Tager JM.
    Eur J Pediatr; 1994; 153(7 Suppl 1):S44-8. PubMed ID: 7957386
    [Abstract] [Full Text] [Related]

  • 26. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.
    Poll-The BT, Skjeldal OH, Stokke O, Poulos A, Demaugre F, Saudubray JM.
    Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.
    Suzuki Y, Shimozawa N, Kawabata I, Yajima S, Inoue K, Uchida Y, Izai K, Tomatsu S, Kondo N, Orii T.
    Brain Dev; 1994 Jan; 16(1):27-31. PubMed ID: 8059925
    [Abstract] [Full Text] [Related]

  • 29. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
    Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A.
    Prog Clin Biol Res; 1990 Jan; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 30. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
    Hoefler G, Hoefler S, Watkins PA, Chen WW, Moser A, Baldwin V, McGillivary B, Charrow J, Friedman JM, Rutledge L.
    J Pediatr; 1988 May; 112(5):726-33. PubMed ID: 2452243
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.
    Balfe A, Hoefler G, Chen WW, Watkins PA.
    Pediatr Res; 1990 Mar; 27(3):304-10. PubMed ID: 2181395
    [Abstract] [Full Text] [Related]

  • 34. The peroxisome and the eye.
    Folz SJ, Trobe JD.
    Surv Ophthalmol; 1991 Mar; 35(5):353-68. PubMed ID: 1710072
    [Abstract] [Full Text] [Related]

  • 35. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B.
    Padiatr Padol; 1993 Mar; 28(1):43-8. PubMed ID: 8446428
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Analysis of very long-chain fatty acids and plasmalogen in the erythrocyte membrane: a simple method for the detection of peroxisomal disorders and discrimination between adrenoleukodystrophy and Zellweger syndrome.
    Tanaka K, Nishizawa K, Yamamoto H, Naruto T, Izeki E, Taga T, Shimada M, Saeki Y.
    Neuropediatrics; 1990 Aug; 21(3):119-23. PubMed ID: 2234315
    [Abstract] [Full Text] [Related]

  • 38. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr; 122(4):573-9. PubMed ID: 8463903
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Metabolism of branched chain fatty acids in peroxisomal disorders.
    Singh H, Usher S, Johnson D, Poulos A.
    J Inherit Metab Dis; 1990 Apr; 13(3):387-9. PubMed ID: 1700192
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.