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 *

24 related articles for article (PubMed ID: 5230213)

  • 1. Biochemical abnormalities of the sarcoplasmic reticulum in muscular dystrophy.
    Samaha FJ; Gergely J
    N Engl J Med; 1969 Jan; 280(4):184-8. PubMed ID: 4235816
    [No Abstract]   [Full Text] [Related]  

  • 2. Abnormal protein synthesis in facioscapulohumeral muscular dystrophy.
    Ionasescu V; Zellweger H; Shirk P; Conway TW
    Neurology; 1972 Dec; 22(12):1286-92. PubMed ID: 4675677
    [No Abstract]   [Full Text] [Related]  

  • 3. [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].
    Radu H; Stenzel K
    Dtsch Z Nervenheilkd; 1969; 196(2):92-115. PubMed ID: 5800957
    [No Abstract]   [Full Text] [Related]  

  • 4. [Medical genetics and enzymes].
    Gedda L
    Recenti Prog Med; 1971 Mar; 50(3):203-14. PubMed ID: 5109832
    [No Abstract]   [Full Text] [Related]  

  • 5. Comparison of ribosomal protein synthesis in Becker and Duchenne muscular dystrophies.
    Ionasescu V; Zellweger H; McCormick WF; Conway TW
    Neurology; 1973 Mar; 23(3):245-53. PubMed ID: 4348618
    [No Abstract]   [Full Text] [Related]  

  • 6. Biochemistry of muscle membranes in Duchenne muscular dystrophy.
    Rowland LP
    Muscle Nerve; 1980; 3(1):3-20. PubMed ID: 6445503
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biochemical aspects of muscle disease.
    Pennington RJ
    Adv Clin Chem; 1971; 14():409-51. PubMed ID: 4944563
    [No Abstract]   [Full Text] [Related]  

  • 8. Dysferlin and muscular dystrophy.
    Bushby KM
    Acta Neurol Belg; 2000 Sep; 100(3):142-5. PubMed ID: 11098285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The comparative utility of serum creatine kinase versus serum aldolase in the evaluation of muscle disorders.
    Giesker D; Bowers GN
    Conn Med; 1979 Nov; 43(11):699-704. PubMed ID: 389542
    [No Abstract]   [Full Text] [Related]  

  • 10. Disturbances of amino acid metabolism in clinical syndromes not characterised by a primary amino acidopathy.
    Bremer HJ; Przyrembel H
    Clin Endocrinol Metab; 1974 Mar; 3(1):131-43. PubMed ID: 4609644
    [No Abstract]   [Full Text] [Related]  

  • 11. Some biochemical changes occurring in muscular dystrophy and their possible genetical significance.
    Monckton G; Nihei T
    Ann N Y Acad Sci; 1966 Sep; 138(1):329-41. PubMed ID: 5230213
    [No Abstract]   [Full Text] [Related]  

  • 12.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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

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

  • 15.
    ; ; . PubMed ID:
    [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 2.