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 *

47 related articles for article (PubMed ID: 5719650)

  • 1. Mental retardation--a clinician's approach to the diagnosis of aminoacidopathies.
    Phadke MA; Gambhir PS; Joshi AS; Limaye AS; Shirole DB; Bapat VS; Padalkar JA
    Indian Pediatr; 1989 Sep; 26(9):921-7. PubMed ID: 2699317
    [No Abstract]   [Full Text] [Related]  

  • 2. Metabolic disorders associated with mental retardation.
    Hsia DY; Berman JL; Justice P; Nadler HL; O'Flynn ME
    Pediatr Clin North Am; 1968 Nov; 15(4):889-904. PubMed ID: 4883204
    [No Abstract]   [Full Text] [Related]  

  • 3. Urinary aminoacids in mental retardation.
    Dhatt PS; Gupta HL; Saini AS
    Indian J Pediatr; 1968 Oct; 35(249):469-75. PubMed ID: 5719650
    [No Abstract]   [Full Text] [Related]  

  • 4. [Amino acid imbalance as a pathogenetic factor in mental retardation (author's transl)].
    Fekete G
    Klin Wochenschr; 1974 May; 52(6):276-82. PubMed ID: 4408538
    [No Abstract]   [Full Text] [Related]  

  • 5. Hereditary disorders of amino acid metabolism associated with mental deficiency.
    Berry HK
    Ann N Y Acad Sci; 1969 Sep; 166(1):66-73. PubMed ID: 5262032
    [No Abstract]   [Full Text] [Related]  

  • 6. Histidinaemia and speech disorders.
    Garvey AM; Gordon N
    Br J Disord Commun; 1969 Oct; 4(2):146-50. PubMed ID: 5366172
    [No Abstract]   [Full Text] [Related]  

  • 7. Hyperuricosuric encephalopathy without hyperuricaemia.
    Hooft C; Van Nevel C; De Schaepdryver AF
    Arch Dis Child; 1968 Dec; 43(232):734-7. PubMed ID: 5702236
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial hyperprolinemia and mental retardation. A second metabolic type.
    Selkoe DJ
    Neurology; 1969 May; 19(5):494-502. PubMed ID: 5815222
    [No Abstract]   [Full Text] [Related]  

  • 9. The pathology and biochemistry of gargoylism; a report of three cases with a review of the literature.
    HENDERSON JL; MacGREGOR AR; THANNHAUSER SJ; HOLDEN R
    Arch Dis Child; 1952 Jun; 27(133):230-53. PubMed ID: 14934278
    [No Abstract]   [Full Text] [Related]  

  • 10. Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.
    Schafer IA; Scriver CR; Efron ML
    N Engl J Med; 1962 Jul; 267():51-60. PubMed ID: 14497974
    [No Abstract]   [Full Text] [Related]  

  • 11. Urinary excretion of beta-amino-isobutyric acid in mongolism.
    PERRY TL; SHAW KN; WALKER D
    Nature; 1959 Dec; 184(Suppl 25)():1970. PubMed ID: 14432043
    [No Abstract]   [Full Text] [Related]  

  • 12. Cystathioniuria.
    HARRIS H; PENROSE LS; THOMAS DH
    Ann Hum Genet; 1959 Dec; 23():442-53. PubMed ID: 14399948
    [No Abstract]   [Full Text] [Related]  

  • 13. PATTERNS OF URINARY AMINO ACIDS IN NORMAL PUNJABIS.
    SAINI AS; SINGH ID; SINGH AI
    Indian J Med Res; 1963 Sep; 51():941-51. PubMed ID: 14065219
    [No Abstract]   [Full Text] [Related]  

  • 14. Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.
    CARSON NA; NEILL DW
    Arch Dis Child; 1962 Oct; 37(195):505-13. PubMed ID: 14018926
    [No Abstract]   [Full Text] [Related]  

  • 15. Aminoaciduria in familial mental retardation.
    POSER CM; BUNCH L
    Arch Neurol; 1963 Jul; 9():35-46. PubMed ID: 13985642
    [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.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 3.