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 *

153 related articles for article (PubMed ID: 4189219)

  • 1. A new mitochondrial myopathy in a patient with salt craving.
    Spiro AJ; Prineas JW; Moore CL
    Arch Neurol; 1970 Mar; 22(3):259-69. PubMed ID: 4189219
    [No Abstract]   [Full Text] [Related]  

  • 2. Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy.
    Schellens JP; Ossentjuk E
    Virchows Arch B Cell Pathol; 1969; 4(1):21-9. PubMed ID: 4242998
    [No Abstract]   [Full Text] [Related]  

  • 3. [Study of a new observation of "nemaline myopathy". II. Ultrastructural findings].
    Fardeau M
    Acta Neuropathol; 1969; 13(3):250-66. PubMed ID: 4185117
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial myopathy with probable lysis of myofibrils in type I fibers.
    Cancilla PA; Kalyanaraman K; Verity MA; Munsat T; Pearson CM
    Neurology; 1971 Jun; 21(6):579-85. PubMed ID: 4104682
    [No Abstract]   [Full Text] [Related]  

  • 5. "Myopathy" with tubular aggregates.
    Lewis PD; Pallis C; Pearse AG
    J Neurol Sci; 1971 Aug; 13(4):381-8. PubMed ID: 4105811
    [No Abstract]   [Full Text] [Related]  

  • 6. Myopathy of hypokalemic periodic paralysis. An electron microscopic study.
    Macdonald RD; Rewcastle NB; Humphrey JG
    Arch Neurol; 1969 Jun; 20(6):565-85. PubMed ID: 5769838
    [No Abstract]   [Full Text] [Related]  

  • 7. McArdle's myopathy. A report of a case with observations on the muscle ultrastructure.
    Brownell B; Hughes JT; Goldby FS; Woods HF
    J Neurol Sci; 1969; 9(3):515-26. PubMed ID: 5367042
    [No Abstract]   [Full Text] [Related]  

  • 8. Emetine myopathy.
    Duane DD; Engel AG
    Neurology; 1970 Aug; 20(8):733-9. PubMed ID: 4195358
    [No Abstract]   [Full Text] [Related]  

  • 9. A new mitochondrial myopathy in a patient with salt craving.
    Spiro AJ; Prineas JW; Moore CL
    Trans Am Neurol Assoc; 1968; 93():283-6. PubMed ID: 5711042
    [No Abstract]   [Full Text] [Related]  

  • 10. Nemaline myopathy: report of a fatal case, with histochemical and electron microscopic studies.
    Shafiq SA; Dubowitz V; Peterson Hde C; Milhorat AT
    Brain; 1967 Dec; 90(4):817-28. PubMed ID: 4169453
    [No Abstract]   [Full Text] [Related]  

  • 11. The myopathy of hyperkalemic periodic paralysis. An electron microscopic study.
    Macdonald RD; Rewcastle NB; Humphrey JG
    Arch Neurol; 1968 Sep; 19(3):274-83. PubMed ID: 5698042
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial myopathy with abnormal muscle mitochondria.
    D'Agostino AN; Ziter FA; Rallison ML; Bray PF
    Arch Neurol; 1968 Apr; 18(4):388-401. PubMed ID: 5638542
    [No Abstract]   [Full Text] [Related]  

  • 13. Mitochondrial myopathy with multisystem abnormalities and normal ocular movements.
    McLeod JG; Baker Wde C; Shorey CD; Kerr CB
    J Neurol Sci; 1975 Jan; 24(1):39-52. PubMed ID: 162937
    [No Abstract]   [Full Text] [Related]  

  • 14. Myopathy associated with abnormal lipid metabolism in skeletal muscle.
    Bradley WG; Hudgson P; Gardner-Medwin D; Walton JN
    Lancet; 1969 Mar; 1(7593):495-8. PubMed ID: 4179573
    [No Abstract]   [Full Text] [Related]  

  • 15. [A case of congenital myopathy with mitochondrial abnormalities. Clinical and ultrastructural study].
    Vallat JM; Aubertin J; Julien J; Vital C; Leng B; Boget JC
    Sem Hop; 1973 Sep; 49(37):2475-82. PubMed ID: 4359500
    [No Abstract]   [Full Text] [Related]  

  • 16. Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.
    Engel AG; Gomez MR; Groover RV
    Mayo Clin Proc; 1971 Oct; 46(10):666-81. PubMed ID: 5115748
    [No Abstract]   [Full Text] [Related]  

  • 17. An electron microscopic study of target fibers, target-like fibers and related abnormalities in human muscle.
    Schotland DL
    J Neuropathol Exp Neurol; 1969 Apr; 28(2):214-28. PubMed ID: 4306866
    [No Abstract]   [Full Text] [Related]  

  • 18. Myopathy associated with linear scleroderma. A histochemical and electron microscopic study.
    Stern LZ; Payne CM; Alvarez JT; Hannapel LK
    Neurology; 1975 Feb; 25(2):114-9. PubMed ID: 163451
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Report of a sub-committee on quantitation of muscle biopsy findings. Appendix B to the Minutes of the Meeting of the Research Group on Neuromuscular Diseases, held in Montreal, Canada, on 21 September, 1967.
    J Neurol Sci; 1968; 6(1):179-88. PubMed ID: 4171326
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary dystonia associated with unique features in skeletal muscle.
    Fenichel GM; Olson WH; Kilroy AW
    Arch Neurol; 1971 Dec; 25(6):552-9. PubMed ID: 5115555
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.