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 *

147 related articles for article (PubMed ID: 16793268)

  • 1. Muscle slowness in a family with nemaline myopathy.
    Pauw-Gommans IM; Gerrits KH; de Haan A; van Engelen BG
    Neuromuscul Disord; 2006 Aug; 16(8):477-80. PubMed ID: 16793268
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Contractile properties of knee-extensors in one single family with nemaline myopathy: central and peripheral aspects of muscle activation.
    Gerrits K; Pauw-Gommans I; van Engelen B; de Haan A
    Clin Physiol Funct Imaging; 2007 Jul; 27(4):217-24. PubMed ID: 17564670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Magnetic resonance imaging of muscle in nemaline myopathy.
    Jungbluth H; Sewry CA; Counsell S; Allsop J; Chattopadhyay A; Mercuri E; North K; Laing N; Bydder G; Pelin K; Wallgren-Pettersson C; Muntoni F
    Neuromuscul Disord; 2004 Dec; 14(12):779-84. PubMed ID: 15564032
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci.
    Jeannet PY; Mittaz L; Dunand M; Lobrinus JA; Bonafe L; Kuntzer T
    Neuromuscul Disord; 2007 Jan; 17(1):6-12. PubMed ID: 17157023
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions.
    Gommans IM; Davis M; Saar K; Lammens M; Mastaglia F; Lamont P; van Duijnhoven G; ter Laak HJ; Reis A; Vogels OJ; Laing N; van Engelen BG; Kremer H
    Brain; 2003 Jul; 126(Pt 7):1545-51. PubMed ID: 12805120
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sporadic late onset nemaline myopathy.
    Chahin N; Selcen D; Engel AG
    Neurology; 2005 Oct; 65(8):1158-64. PubMed ID: 16148261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele.
    Garcia-Angarita N; Kirschner J; Heiliger M; Thirion C; Walter MC; Schnittfeld-Acarlioglu S; Albrecht M; Müller K; Wieczorek D; Lochmüller H; Krause S
    Neuromuscul Disord; 2009 Jul; 19(7):481-4. PubMed ID: 19553116
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).
    Wallefeld W; Krause S; Nowak KJ; Dye D; Horváth R; Molnár Z; Szabó M; Hashimoto K; Reina C; De Carlos J; Rosell J; Cabello A; Navarro C; Nishino I; Lochmüller H; Laing NG
    Neuromuscul Disord; 2006 Oct; 16(9-10):541-7. PubMed ID: 16945536
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intranuclear nemaline rod myopathy.
    Kaimaktchiev V; Goebel H; Laing N; Narus M; Weeks D; Nixon R
    Muscle Nerve; 2006 Sep; 34(3):369-72. PubMed ID: 16477620
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.
    Agrawal PB; Strickland CD; Midgett C; Morales A; Newburger DE; Poulos MA; Tomczak KK; Ryan MM; Iannaccone ST; Crawford TO; Laing NG; Beggs AH
    Ann Neurol; 2004 Jul; 56(1):86-96. PubMed ID: 15236405
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Muscle weakness in a mouse model of nemaline myopathy can be reversed with exercise and reveals a novel myofiber repair mechanism.
    Joya JE; Kee AJ; Nair-Shalliker V; Ghoddusi M; Nguyen MA; Luther P; Hardeman EC
    Hum Mol Genet; 2004 Nov; 13(21):2633-45. PubMed ID: 15367485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A comparative study of the clinical and histological characteristics between classic nemaline myopathy and that associated with the human immunodeficiency virus].
    Miró O; Masanés F; Pedrol E; García-Carrasco M; Mallolas J; Casademont J; Grau JM
    Med Clin (Barc); 1995 Oct; 105(13):500-3. PubMed ID: 7494440
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy.
    Monnier N; Lunardi J; Marty I; Mezin P; Labarre-Vila A; Dieterich K; Jouk PS
    Neuromuscul Disord; 2009 Feb; 19(2):118-23. PubMed ID: 19155175
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HIV-associated nemaline rod myopathy: role of intravenous immunoglobulin therapy in two persons with HIV/AIDS.
    de Sanctis JT; Cumbo-Nacheli G; Dobbie D; Baumgartner D
    AIDS Read; 2008 Feb; 18(2):90-4. PubMed ID: 18330038
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dietary L-tyrosine supplementation in nemaline myopathy.
    Ryan MM; Sy C; Rudge S; Ellaway C; Ketteridge D; Roddick LG; Iannaccone ST; Kornberg AJ; North KN
    J Child Neurol; 2008 Jun; 23(6):609-13. PubMed ID: 18079309
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case of neuromuscular mimicry.
    Bos MM; Overeem S; van Engelen BG; Scheffer H; van den Elzen C; Ter Laak H; Lammens M; Schelhaas HJ; Zwarts MJ
    Neuromuscul Disord; 2006 Aug; 16(8):510-3. PubMed ID: 16919950
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.