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

112 related items for PubMed ID: 5006283

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [The familial incidence of epilepsy in the group of epileptic patients examined after their first seizure--pilot study].
    Rózsavölgyi M, Rajna P.
    Ideggyogy Sz; 2007 Jan 20; 60(1-2):23-9. PubMed ID: 17432090
    [Abstract] [Full Text] [Related]

  • 4. Urinary excretion of aminoacids in mentally retarded children. A study of 150 cases by circular paper chromatography.
    Gupta PC, Nath A, Virmani V.
    Neurol India; 1970 Mar 20; 18(1):17-21. PubMed ID: 5439380
    [No Abstract] [Full Text] [Related]

  • 5. Familial hyperinsulinaemia associated with epilepsy and mental retardation--a syndrome of familial insulin resistance.
    Idris I, Miller D, Page SR.
    Diabet Med; 2004 Jun 20; 21(6):628-31. PubMed ID: 15154952
    [Abstract] [Full Text] [Related]

  • 6. [Further results of studies on metabolic disorders in a population of severely retarded children (2)].
    Opałka S, Galewicz A, Pisarska E, Wegrzynowicz Z.
    Psychiatr Neurol Med Psychol Beih; 1968 Jun 20; 8-9():126-9. PubMed ID: 5006367
    [Abstract] [Full Text] [Related]

  • 7. [Neuropsychiatric disorders in children whose relatives have epilepsy].
    Rogacheva TA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1985 Jun 20; 85(6):871-4. PubMed ID: 4024811
    [Abstract] [Full Text] [Related]

  • 8. [Changes in metabolism of tryptophan of a familial type with mental deficiency].
    Giovannini M, Careddu P.
    Pediatria (Napoli); 1967 Jun 20; 75(1):48-59. PubMed ID: 5601245
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Familial richner-Hanhart syndrome in Kuwait: twelve-year clinical reassessment by a multidisciplinary approach.
    el-Badramany MH, Fawzy AR, Farag TI.
    Am J Med Genet; 1995 Oct 09; 60(5):353-5. PubMed ID: 8546145
    [No Abstract] [Full Text] [Related]

  • 11. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
    Terheggen HG, Schwenk A, Lowenthal A, van Sande M, Colombo JP.
    Z Kinderheilkd; 1970 Oct 09; 107(4):313-23. PubMed ID: 5438972
    [No Abstract] [Full Text] [Related]

  • 12. The Vodskov project. 3. Thin-layer chromatography of amino acids in urine from mentally retarded patients. Methodology of the investigation.
    Andersen HE, Bang HO.
    Dan Med Bull; 1969 Sep 09; 16(8):235-8. PubMed ID: 5377695
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Aspartylglycosaminuria. Analysis of thirty-four patients.
    Autio S.
    J Ment Defic Res; 1972 Sep 09; 1(0):1-93. PubMed ID: 4606247
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 09; 44(5):655-60. PubMed ID: 5374976
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.