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 *

66 related articles for article (PubMed ID: 4727605)

  • 1. [Saccharopinuria].
    Bovier-Lapierre M
    Pediatrie; 1973 Jun; 28(4):459-63. PubMed ID: 4727605
    [No Abstract]   [Full Text] [Related]  

  • 2. Hyperlysinemia associated with retardation.
    Ghadimi H; Binnington VI; Pecora P
    N Engl J Med; 1965 Sep; 273(14):723-9. PubMed ID: 5825685
    [No Abstract]   [Full Text] [Related]  

  • 3. [A patient with persistent hyperlysinemia].
    Sengers RC; Trijbels JM; Corstiaensen JB
    Tijdschr Kindergeneeskd; 1983 Feb; 51(1):24-6. PubMed ID: 6407142
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    Shih VE; Efron ML; Moser HW
    Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534
    [No Abstract]   [Full Text] [Related]  

  • 5. [Inborn errors of lysine metabolism].
    Divry P; Vianey-Liaud C; Mathieu M
    Ann Biol Clin (Paris); 1991; 49(1):27-35. PubMed ID: 1904694
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The pathogenesis of mental retardation in phenylketonuria and other inborn errors of amino acid metabolism.
    Menkes JH
    Pediatrics; 1967 Feb; 39(2):297-308. PubMed ID: 5335144
    [No Abstract]   [Full Text] [Related]  

  • 7. [Saccharopinuria (a variant form of familial hyperlysinemia)].
    Higashino K
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):191-4. PubMed ID: 9590025
    [No Abstract]   [Full Text] [Related]  

  • 8. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies].
    Thiriar MJ; Szliwowski HB; Vis HL
    Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603
    [No Abstract]   [Full Text] [Related]  

  • 9. Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population.
    Hyánek J; Homolka J; Seemanová E
    Rev Czech Med; 1974; 20(1):18-22. PubMed ID: 4815837
    [No Abstract]   [Full Text] [Related]  

  • 10. Saccharopinuria.
    Simell O; Visakorpi JK; Donner M
    Arch Dis Child; 1972 Feb; 47(251):52-5. PubMed ID: 5018656
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of hyperlysinemia: biochemical and clinical observations.
    Armstrong MD; Robinow M
    Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933
    [No Abstract]   [Full Text] [Related]  

  • 12. Intestinal absorption of L-arginine and L-lysine in familial protein intolerance.
    Kekomäki M
    Ann Paediatr Fenn; 1968; 14(1):18-22. PubMed ID: 5685037
    [No Abstract]   [Full Text] [Related]  

  • 13. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

  • 14. [The detection of aminoacidopathies causing mental retardation].
    Thiriar M; Vis HL
    Acta Paediatr Belg; 1966; 20(5):333-70. PubMed ID: 5330633
    [No Abstract]   [Full Text] [Related]  

  • 15. Enzyme defect in saccharopinuria.
    Simell O; Johansson T; Aula P
    J Pediatr; 1973 Jan; 82(1):54-7. PubMed ID: 4404606
    [No Abstract]   [Full Text] [Related]  

  • 16. [Homocystinuria].
    Hagberg B; Hambraeus L
    Lakartidningen; 1967 Jul; 64(29):2893-902. PubMed ID: 5597594
    [No Abstract]   [Full Text] [Related]  

  • 17. Mental retardation due to inborn errors of amino acid metabolism in Puerto Rico. Results of a screening test and a review of other documented cases.
    Crosby PF
    Bol Asoc Med P R; 1971 Jul; 63(7):184-6. PubMed ID: 5286510
    [No Abstract]   [Full Text] [Related]  

  • 18. [Study of urinary elimination of amino acids in infantile cerebral diseases].
    Zoratto E; Cocuzza S; Lumare A
    Minerva Pediatr; 1965 Oct; 17(31):1646-51. PubMed ID: 5858644
    [No Abstract]   [Full Text] [Related]  

  • 19. Screening for aminoacid disorders in mental retardation.
    Jyothy A; Reddy PP
    Indian Pediatr; 1984 May; 21(5):381-8. PubMed ID: 6480090
    [No Abstract]   [Full Text] [Related]  

  • 20. Prevalence of homocystinuria among the mentally retarded: evaluation of a specific screening test.
    Spaeth GL; Barber GW
    Pediatrics; 1967 Oct; 40(4):586-9. PubMed ID: 6051058
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.