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 *

126 related articles for article (PubMed ID: 11206338)

  • 1. Nemaline cardiomyopathy in a young adult: an ultraimmunohistochemical study and review of the literature.
    Müller-Höcker J; Schäfer S; Mendel B; Lochmüller H; Pongratz D
    Ultrastruct Pathol; 2000; 24(6):407-16. PubMed ID: 11206338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy.
    Wallgren-Pettersson C; Jasani B; Newman GR; Morris GE; Jones S; Singhrao S; Clarke A; Virtanen I; Holmberg C; Rapola J
    Neuromuscul Disord; 1995 Mar; 5(2):93-104. PubMed ID: 7767098
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nemaline rod and central core disease: a coexisting Z-band myopathy.
    Thomas C
    Muscle Nerve; 1997 Jul; 20(7):893-6. PubMed ID: 9179165
    [No Abstract]   [Full Text] [Related]  

  • 4. Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rods.
    Schröder R; Reimann J; Salmikangas P; Clemen CS; Hayashi YK; Nonaka I; Arahata K; Carpén O
    Neuromuscul Disord; 2003 Aug; 13(6):451-5. PubMed ID: 12899871
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical course correlates poorly with muscle pathology in nemaline myopathy.
    Ryan MM; Ilkovski B; Strickland CD; Schnell C; Sanoudou D; Midgett C; Houston R; Muirhead D; Dennett X; Shield LK; De Girolami U; Iannaccone ST; Laing NG; North KN; Beggs AH
    Neurology; 2003 Feb; 60(4):665-73. PubMed ID: 12601110
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nemaline rod and degeneration of Z band of muscle cell in weightlessness at spaceflight.
    Imuta M; Higuchi I
    Acta Astronaut; 1999 Mar; 44(5-6):307-11. PubMed ID: 11541952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nemaline myopathy with intranuclear rods--intranuclear rod myopathy.
    Goebel HH; Warlo I
    Neuromuscul Disord; 1997 Jan; 7(1):13-9. PubMed ID: 9132135
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).
    Ohlsson M; Tajsharghi H; Darin N; Kyllerman M; Oldfors A
    Neuromuscul Disord; 2004 Sep; 14(8-9):471-5. PubMed ID: 15336687
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Restrictive cardiomyopathy, atrioventricular block and mild to subclinical myopathy in patients with desmin-immunoreactive material deposits.
    Arbustini E; Morbini P; Grasso M; Fasani R; Verga L; Bellini O; Dal Bello B; Campana C; Piccolo G; Febo O; Opasich C; Gavazzi A; Ferrans VJ
    J Am Coll Cardiol; 1998 Mar; 31(3):645-53. PubMed ID: 9502648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation.
    Kim SY; Park YE; Kim HS; Lee CH; Yang DH; Kim DS
    J Neurol Sci; 2011 Aug; 307(1-2):171-3. PubMed ID: 21570694
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial cardioneuromyopathy with hyaline masses and nemaline rods: a novel phenotype.
    Selcen D; Krueger BR; Engel AG
    Ann Neurol; 2002 Feb; 51(2):224-34. PubMed ID: 11835379
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ultrastructural and biochemical localization of N-RAP at the interface between myofibrils and intercalated disks in the mouse heart.
    Zhang JQ; Elzey B; Williams G; Lu S; Law DJ; Horowits R
    Biochemistry; 2001 Dec; 40(49):14898-906. PubMed ID: 11732910
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Intranuclear rod myopathy, a rare and morphologically striking variant of nemaline rod myopathy.
    Weeks DA; Nixon RR; Kaimaktchiev V; Mierau GW
    Ultrastruct Pathol; 2003; 27(3):151-4. PubMed ID: 12775505
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Nemaline myopathy: report of a case].
    Wu HR; Liu X; Sun LY; Bu Y; Guo YS; Wu DX; Song XQ
    Zhonghua Bing Li Xue Za Zhi; 2013 Jun; 42(6):407-8. PubMed ID: 24060078
    [No Abstract]   [Full Text] [Related]  

  • 15. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred.
    Hutchinson DO; Charlton A; Laing NG; Ilkovski B; North KN
    Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.
    D'Amico A; Graziano C; Pacileo G; Petrini S; Nowak KJ; Boldrini R; Jacques A; Feng JJ; Porfirio B; Sewry CA; Santorelli FM; Limongelli G; Bertini E; Laing N; Marston SB
    Neuromuscul Disord; 2006 Oct; 16(9-10):548-52. PubMed ID: 16945537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.
    Sztal TE; Zhao M; Williams C; Oorschot V; Parslow AC; Giousoh A; Yuen M; Hall TE; Costin A; Ramm G; Bird PI; Busch-Nentwich EM; Stemple DL; Currie PD; Cooper ST; Laing NG; Nowak KJ; Bryson-Richardson RJ
    Acta Neuropathol; 2015 Sep; 130(3):389-406. PubMed ID: 25931053
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sarcomeric-alpha-actinin defective in vinculin-binding causes Z-line expansion and nemaline-like body formation in cultured chick myotubes.
    Zhang ZQ; Bish LT; Holtzer H; Sweeney HL
    Exp Cell Res; 2009 Mar; 315(5):748-59. PubMed ID: 19166831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Centronuclear Myopathy with Abundant Nemaline Rods in a Japanese Black and Hereford Crossbred Calf.
    Kamio K; Takahashi Y; Ishihara K; Sekiya A; Kato S; Shimanuki I; Ide M; Furuoka H
    J Comp Pathol; 2020 Jan; 174():8-12. PubMed ID: 31955807
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn).
    Schröder JM; Durling H; Laing N
    Acta Neuropathol; 2004 Sep; 108(3):250-6. PubMed ID: 15221331
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.