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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 1779646)

  • 1. Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine.
    Roesel RA; Carroll JE; Rizzo WB; van der Zalm T; Hahn DA
    J Inherit Metab Dis; 1991; 14(6):876-80. PubMed ID: 1779646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction.
    Poll-The BT; Saudubray JM; Ogier H; Schutgens RB; Wanders RJ; Schrakamp G; van den Bosch H; Trijbels JM; Poulos A; Moser HW
    J Inherit Metab Dis; 1986; 9(2):169-74. PubMed ID: 2427795
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.
    Wanders RJ; Heymans HS; Schutgens RB; Poll-Thé BT; Saudubray JM; Tager JM; Schrakamp G; van den Bosch H
    J Neurol Sci; 1988 Apr; 84(2-3):147-55. PubMed ID: 2454298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.
    Wanders RJ; van Roermund CW; van Wijland MJ; Schutgens RB; Tager JM; van den Bosch H; Thomas GH
    J Inherit Metab Dis; 1988; 11 Suppl 2():161-4. PubMed ID: 3141699
    [No Abstract]   [Full Text] [Related]  

  • 5. 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; 10 Suppl 1():33-45. PubMed ID: 3119940
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Peroxisomal disorders; newer concept and recent studies].
    Kamoshita S
    Nihon Rinsho; 1990 Mar; 48(3):629-38. PubMed ID: 2192101
    [No Abstract]   [Full Text] [Related]  

  • 7. [Biochemistry of peroxisome and peroxisomal diseases].
    Vamecq J; Poll-The BT; Saudubray JM
    Ann Biol Clin (Paris); 1988; 46(4):233-58. PubMed ID: 3389578
    [No Abstract]   [Full Text] [Related]  

  • 8. Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.
    Baumgartner MR; Verhoeven NM; Jakobs C; Roels F; Espeel M; Martinez M; Rabier D; Wanders RJ; Saudubray JM
    Neurology; 1998 Nov; 51(5):1427-32. PubMed ID: 9818873
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P; Kremser K; Roland MO; Rocchiccioli F; Singh I
    Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis.
    Smeitink JA; Beemer FA; Espeel M; Donckerwolcke RA; Jakobs C; Wanders RJ; Schutgens RB; Roels F; Duran M; Dorland L
    J Inherit Metab Dis; 1992; 15(3):377-80. PubMed ID: 1405474
    [No Abstract]   [Full Text] [Related]  

  • 11. Biochemistry of peroxisomes in health and disease.
    Singh I
    Mol Cell Biochem; 1997 Feb; 167(1-2):1-29. PubMed ID: 9059978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new peroxisomal disease with impaired phytanic and pipecolic acid oxidation.
    Tranchant C; Aubourg P; Mohr M; Rocchiccioli F; Zaenker C; Warter JM
    Neurology; 1993 Oct; 43(10):2044-8. PubMed ID: 8413964
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Dyggve-Melchior-Clausen syndrome.
    Rastogi SC; Clausen J; Melchior JC; Dyggve HV
    Clin Chim Acta; 1977 Jul; 78(1):55-69. PubMed ID: 141987
    [No Abstract]   [Full Text] [Related]  

  • 14. Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children.
    Budden SS; Kennaway NG; Buist NR; Poulos A; Weleber RG
    J Pediatr; 1986 Jan; 108(1):33-9. PubMed ID: 2418187
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biochemical abnormalities in Dyggve-Melchior-Clausen syndrome.
    Rastogi SC; Clausen J; Melchior JC; Dyggve HV
    Clin Chim Acta; 1978 Mar; 84(1-2):173-8. PubMed ID: 639301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An extremely rare association of dyggve-melchior-clausen syndrome with mania: coincidence or comorbidity.
    Kar SK; Bansal S; Kumar D
    Indian J Psychol Med; 2015; 37(2):226-9. PubMed ID: 25969613
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease].
    Coëslier A; Boute-Bénéjean O; Moerman A; Fron D; Manouvrier-Hanu S
    Arch Pediatr; 2001 Aug; 8(8):838-42. PubMed ID: 11524915
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Dyggve-Melchior-Clausen syndrome.
    Spranger J; Maroteaux P; Der Kaloustian VM
    Radiology; 1975 Feb; 114(2):415-21. PubMed ID: 803318
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Treatment of hip subluxation in Dyggve-Melchior-Clausen syndrome.
    Hosny GA; Fabry G
    J Pediatr Orthop B; 1998 Jan; 7(1):32-4. PubMed ID: 9481654
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.