BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 6846734)

  • 1. Early infant death in nemaline (rod) myopathy.
    Eeg-Olofsson O; Henriksson KG; Thornell LE; Wesström G
    Brain Dev; 1983; 5(1):53-7. PubMed ID: 6846734
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fatal neonatal nemaline myopathy.
    Matsuo T; Tashiro T; Ikeda T; Tsujihata M; Shimomura C
    Acta Pathol Jpn; 1982 Sep; 32(5):907-16. PubMed ID: 6182741
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Rod myopathy. A fatal neonatal case].
    Netter JC; Laurent-Pellegrin M; Bildstein G; Chateauneuf R; Petrus M
    Arch Fr Pediatr; 1986 May; 43(5):327-9. PubMed ID: 3778091
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.
    Berger J; Tarakci H; Berger S; Li M; Hall TE; Arner A; Currie PD
    Dis Model Mech; 2014 Dec; 7(12):1407-15. PubMed ID: 25288681
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [A case of severe infantile form of congenital nemaline myopathy with extensive fatty replacement of the skeletal muscles].
    Shimizu J; Matsumura K; Noguchi H
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1123-7. PubMed ID: 2177691
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A study of a myopathy presenting as idiopathic scoliosis. Multicore disease or mitochondrial myopathy?
    Fitzsimons RB; Tyer HD
    J Neurol Sci; 1980 Apr; 46(1):33-48. PubMed ID: 7373343
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Nemaline myopathy.
    Greenwood SM; Viozzi FJ
    Arch Pathol Lab Med; 1978 Apr; 102(4):196-200. PubMed ID: 580714
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Nemaline myopathy (clinico-morphologic study)].
    Il'ina NA; Sokolina NA; Aver'ianov IuN; Korolev VV; Golovakina AN
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1447-50. PubMed ID: 716716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neonatal nemaline myopathy with abundant intranuclear rods.
    Barohn RJ; Jackson CE; Kagan-Hallet KS
    Neuromuscul Disord; 1994; 4(5-6):513-20. PubMed ID: 7881297
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Nemaline myopathy: an unusual course].
    Dóczy LC; Morscher M; Schmitzberger R; Willeit J; Haberfellner H
    Padiatr Padol; 1991; 26(1):49-51. PubMed ID: 1647515
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nemaline myopathy rod bodies. Structure and composition.
    Yamaguchi M; Robson RM; Stromer MH; Dahl DS; Oda T
    J Neurol Sci; 1982 Oct; 56(1):35-56. PubMed ID: 6754876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Sporadic Z disk myopathy with accumulation of rods and cytoplasmic bodies].
    Gérard JM; Telerman-Toppet N; Borenstein S; Flament-Durand J
    Rev Neurol (Paris); 1991; 147(2):144-7. PubMed ID: 2028148
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.
    Scacheri PC; Hoffman EP; Fratkin JD; Semino-Mora C; Senchak A; Davis MR; Laing NG; Vedanarayanan V; Subramony SH
    Neurology; 2000 Dec; 55(11):1689-96. PubMed ID: 11113224
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigations on the inheritance of nemaline myopathy.
    Arts WF; Bethlem J; Dingemans KP; Eriksson AW
    Arch Neurol; 1978 Feb; 35(2):72-7. PubMed ID: 623532
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The fine structure of the rod-like bodies in nemaline myopathy and their relation to the Z-discs.
    Gonatas NK
    J Neuropathol Exp Neurol; 1966 Jul; 25(3):409-21. PubMed ID: 5946176
    [No Abstract]   [Full Text] [Related]  

  • 18. [Sibling cases of severe infantile form of nemaline myopathy with ACTA1-gene mutation].
    Sudo A; Hayashi Y; Sano H; Kawamura N; Nishino I; Nonaka I
    No To Hattatsu; 2013 Nov; 45(6):452-6. PubMed ID: 24313005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study.
    Ishibashi-Ueda H; Imakita M; Yutani C; Takahashi S; Yazawa K; Kamiya T; Nonaka I
    Hum Pathol; 1990 Jan; 21(1):77-82. PubMed ID: 2295510
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neonatal nemaline myopathy presenting with multiple joint contractures.
    Bucher HU; Boltshauser E; Briner J
    Eur J Pediatr; 1985 Sep; 144(3):288-90. PubMed ID: 2414108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.