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 *

304 related articles for article (PubMed ID: 11989852)

  • 61. Autosomal dominant distal myopathy with nemaline rods due to p.Glu197Asp mutation in ACTA1.
    Hernandez-Lain A; Cantero D; Camacho-Salas A; Toldos O; Esteban I; Pascual I; Dominguez-Gonzalez C
    Neuromuscul Disord; 2019 Mar; 29(3):247-250. PubMed ID: 30732915
    [TBL] [Abstract][Full Text] [Related]  

  • 62. [Two adult cases of nemaline myopathy presenting different clinical symptoms and CT findings].
    Tajima Y; Yoshida A; Ura S
    No To Shinkei; 2001 Jul; 53(7):653-8. PubMed ID: 11517491
    [TBL] [Abstract][Full Text] [Related]  

  • 63. HIV, rods, and the muscles--a discussion about HIV-associated nemaline rod myopathy.
    Madonia P; Wilson J; Bican O; Willis M; Bass P
    J La State Med Soc; 2012; 164(6):320-3. PubMed ID: 23431674
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.
    Monforte M; Primiano G; Silvestri G; Mirabella M; Luigetti M; Cuccagna C; Ricci E; Servidei S; Tasca G
    J Neurol; 2018 Mar; 265(3):542-551. PubMed ID: 29356967
    [TBL] [Abstract][Full Text] [Related]  

  • 65. [Nemaline rod myopathy revealed by acute respiratory failure after an outpatient cataract surgery].
    Raveau T; Lassalle V; Dubourg O; Legout A; Tirot P
    Ann Fr Anesth Reanim; 2012; 31(7-8):638-40. PubMed ID: 22749553
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Recent advances in nemaline myopathy.
    Romero NB; Sandaradura SA; Clarke NF
    Curr Opin Neurol; 2013 Oct; 26(5):519-26. PubMed ID: 23995272
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
    Pénisson-Besnier I; Monnier N; Toutain A; Dubas F; Laing N
    Neuromuscul Disord; 2007 Apr; 17(4):330-7. PubMed ID: 17376686
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Nemaline myopathy: two autopsy reports.
    Bergmann M; Kamarampaka M; Kuchelmeister K; Klein H; Koch H
    Childs Nerv Syst; 1995 Oct; 11(10):610-5. PubMed ID: 8556730
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Severe congenital nemaline myopathy: a personal perspective.
    Marinone K
    Neonatal Netw; 1998 Feb; 17(1):29-32. PubMed ID: 9526359
    [TBL] [Abstract][Full Text] [Related]  

  • 70. [Two cases of nemaline myopathy diagnosed after episodes of respiratory failure].
    Kudou M; Kobayashi Y; Yamashita K; Kita H; Yasuba H; Hamada K
    Nihon Kokyuki Gakkai Zasshi; 2006 Jun; 44(6):474-8. PubMed ID: 16841721
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Sudden cardiac arrest in a child with nemaline myopathy.
    Marseglia L; D'Angelo G; Manti S; Salpietro V; Arrigo T; Cavallari V; Gitto E
    Ital J Pediatr; 2015 Mar; 41():20. PubMed ID: 25888334
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Severe infantile congenital myopathy with nemaline and cytoplasmic bodies: a case report.
    Itakura Y; Ogawa Y; Murakami N; Nonaka I
    Brain Dev; 1998 Mar; 20(2):112-5. PubMed ID: 9545182
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Novel presentation of central core disease with nemaline bodies (rods) in the setting of diploid/triploid mosaicism.
    Shafi NB; Parker JC; Atkinson JB; Parker JR
    Ann Clin Lab Sci; 2007; 37(2):177-81. PubMed ID: 17522375
    [TBL] [Abstract][Full Text] [Related]  

  • 74. An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
    Corbett MA; Akkari PA; Domazetovska A; Cooper ST; North KN; Laing NG; Gunning PW; Hardeman EC
    Ann Neurol; 2005 Jan; 57(1):42-9. PubMed ID: 15562513
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin.
    Wallgren-Pettersson C; Pelin K; Nowak KJ; Muntoni F; Romero NB; Goebel HH; North KN; Beggs AH; Laing NG;
    Neuromuscul Disord; 2004 Sep; 14(8-9):461-70. PubMed ID: 15336686
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Distinct light microscopic changes in human immunodeficiency virus-associated nemaline myopathy.
    Feinberg DM; Spiro AJ; Weidenheim KM
    Neurology; 1998 Feb; 50(2):529-31. PubMed ID: 9484391
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Quadriceps weakness in a family with nemaline myopathy: influence of knee angle.
    Gerrits K; Gommans I; van Engelen B; de Haan A
    Clin Sci (Lond); 2003 Nov; 105(5):585-9. PubMed ID: 12848616
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thrive.
    Lamont PJ; Thorburn DR; Fabian V; Vajsar J; Hawkins C; Saada Reisch A; Durling H; Laing NG; Nevo Y
    Neuropediatrics; 2004 Oct; 35(5):302-6. PubMed ID: 15534765
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Editorial comment: HIV-associated adult-onset nemaline myopathy.
    Mani D; Aboulafia DM
    AIDS Read; 2008 Feb; 18(2):100-1. PubMed ID: 18330039
    [No Abstract]   [Full Text] [Related]  

  • 80. Congenital myopathy with ringlike distribution of myonuclei and mitochondria and accumulation of nemaline rods. A variant of centronuclear myopathy?
    Waclawik AJ; Edgar TS; Lotz BP; Lewandoski P; Rust RS
    Pediatr Neurol; 1995 May; 12(4):370-3. PubMed ID: 7546014
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.