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 *

123 related articles for article (PubMed ID: 1822796)

  • 1. An adult-onset myopathy characterized by a double ring appearance of muscle fibers.
    Coulter CL; Marks WA; Bodensteiner JB; Leech RW; Tonin P; DiMauro S; Brumback RA
    Neuromuscul Disord; 1991; 1(3):205-9. PubMed ID: 1822796
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult onset nemaline myopathy: a distinct nosologic entity?
    Palmucci L; Doriguzzi C; Mongini T; Chiadò-Piat L
    Clin Neuropathol; 1993; 12(3):153-5. PubMed ID: 8391957
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Electronmicroscopy in the study of disorders of skeletal muscle.
    Fisher ER; Danowski TS
    Pathol Annu; 1974; 9(0):345-84. PubMed ID: 4609269
    [No Abstract]   [Full Text] [Related]  

  • 4. Debrancher deficiency: neuromuscular disorder in 5 adults.
    DiMauro S; Hartwig GB; Hays A; Eastwood AB; Franco R; Olarte M; Chang M; Roses AD; Fetell M; Schoenfeldt RS; Stern LZ
    Ann Neurol; 1979 May; 5(5):422-36. PubMed ID: 288318
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Ultrastructural elementary lesions in muscular pathology (author's transl)].
    Tassin S; Brucher JM
    Acta Neurol Belg; 1981; 81(2):106-18. PubMed ID: 7234320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The significance of target fibers: a clinicopathologic review of 100 patients with neurogenic atrophy.
    Kovarsky J; Schochet SS; McCormick WF
    Am J Clin Pathol; 1973 Jun; 59(6):790-7. PubMed ID: 4122677
    [No Abstract]   [Full Text] [Related]  

  • 7. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria.
    Tamura K; Santa T; Kuroiwa Y
    Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795
    [No Abstract]   [Full Text] [Related]  

  • 8. A unique case of reducing body myopathy.
    Nomizu S; Person DA; Saito C; Lockett LJ
    Muscle Nerve; 1992 Apr; 15(4):463-6. PubMed ID: 1314327
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ultrastructural changes in human muscle fibres in disease.
    Papadimitriou JM; Mastaglia FL
    J Submicrosc Cytol; 1982 Jul; 14(3):525-51. PubMed ID: 6757457
    [No Abstract]   [Full Text] [Related]  

  • 10. A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line.
    Pellegrini G; Barbieri S; Moggio M; Cheldi A; Scarlato G; Minetti C
    Neuropediatrics; 1985 Aug; 16(3):162-6. PubMed ID: 4047349
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Fine structure of prenatal and early postnatal dystrophic mouse muscle.
    Platzer AC; Powell JA
    J Neurol Sci; 1975 Jan; 24(1):109-26. PubMed ID: 1110369
    [No Abstract]   [Full Text] [Related]  

  • 13. [Ultrastructural characteristics of tubular aggregates in human skeletal muscles].
    Babakova LL; Kolomenskaia EA; Kuz'min NV; Pozdniakov OM
    Arkh Patol; 1974; 36(4):50-6. PubMed ID: 4457084
    [No Abstract]   [Full Text] [Related]  

  • 14. Fatal reducing body myopathy. Ultrastructural and immunohistochemical observations.
    Kiyomoto BH; Murakami N; Kobayashi Y; Nihei K; Tanaka T; Takeshita K; Nonaka I
    J Neurol Sci; 1995 Jan; 128(1):58-65. PubMed ID: 7722535
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant neuromuscular disease with cylindrical spirals.
    Taratuto AL; Matteucci M; Barreiro C; Saccolitti M; Sevlever G
    Neuromuscul Disord; 1991; 1(6):433-41. PubMed ID: 1822355
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type.
    Gibbels E; Kellermann K; Schädlich HJ; Adams R; Haupt WF
    Acta Neuropathol; 1992; 83(4):371-8. PubMed ID: 1575014
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuronal changes of hypokalemic myopathy. A light- and electron-microscopic study on muscle biopsy.
    Hashimoto S; Akai F; Semba E; Sakatani K; Hiruma S; Nagaoka M; Hukuda K; Imada A
    J Neurol Sci; 1980 Jan; 44(2-3):169-79. PubMed ID: 7354366
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new familial congenital myopathy in children with desmin and dystrophin reacting plaques.
    Fidziańska A; Ryniewicz B; Barcikowska M; Goebel HH
    J Neurol Sci; 1995 Jul; 131(1):88-95. PubMed ID: 7561954
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The syndrome of 'continuous muscle-fibre activity' cured: further studies.
    Isaacs H; Heffron JJ
    J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1231-5. PubMed ID: 4281819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lobulated fibers in neuromuscular diseases.
    Guerard MJ; Sewry CA; Dubowitz V
    J Neurol Sci; 1985 Jul; 69(3):345-56. PubMed ID: 3162002
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.