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)

  • 41. Neonatal-onset nemaline myopathy mimicking congenital diaphragmatic hernia.
    Danhaive O; Lozzi S; D'amico A; Devito R; Boldrini R; Corchia C; Bagolan P; Bertini E
    J Pediatr Surg; 2007 Jul; 42(7):E19-22. PubMed ID: 17618867
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. 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]  

  • 44. [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]  

  • 45. Clinical and pathological features of patients with nemaline myopathy.
    Yin X; Pu CQ; Wang Q; Liu JX; Mao YL
    Mol Med Rep; 2014 Jul; 10(1):175-82. PubMed ID: 24788569
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Adult onset nemaline myopathy revealed by respiratory insufficiency].
    Befort P; Landreau L; Pagès AM; Jonquet O; Pagès M
    Rev Neurol (Paris); 2006 Dec; 162(12):1260-2. PubMed ID: 17151520
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Two cases of sporadic late onset nemaline myopathy effectively treated with immunotherapy].
    Mizuno Y; Mori-Yoshimura M; Okamoto T; Oya Y; Nishino I; Murata M
    Rinsho Shinkeigaku; 2016 Sep; 56(9):605-11. PubMed ID: 27580764
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Congenital nemaline myopathy due to ACTA1-gene mutation and carnitine insufficiency: a case report.
    Buxmann H; Schlösser R; Schlote W; Sewell A; Nowak KJ; Laing NG; Loewenich V
    Neuropediatrics; 2001 Oct; 32(5):267-70. PubMed ID: 11748499
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Nemaline myopathies: State of the art.
    Malfatti E; Romero NB
    Rev Neurol (Paris); 2016 Oct; 172(10):614-619. PubMed ID: 27659899
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Dropped head syndrome secondary to nemalinic myopathy].
    Erro M; Echávarri C; Tuñón T
    Neurologia; 2006 Sep; 21(7):376-7. PubMed ID: 16977558
    [No Abstract]   [Full Text] [Related]  

  • 51. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
    Schnitzler LJ; Schreckenbach T; Nadaj-Pakleza A; Stenzel W; Rushing EJ; Van Damme P; Ferbert A; Petri S; Hartmann C; Bornemann A; Meisel A; Petersen JA; Tousseyn T; Thal DR; Reimann J; De Jonghe P; Martin JJ; Van den Bergh PY; Schulz JB; Weis J; Claeys KG
    Orphanet J Rare Dis; 2017 May; 12(1):86. PubMed ID: 28490364
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Adult nemaline myopathy with trabecular muscle fibers.
    Irodenko VS; Lee HS; de Armond SJ; Layzer RB
    Muscle Nerve; 2009 Jun; 39(6):871-5. PubMed ID: 19229965
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Adult-onset of nemaline myopathy, associated with cores and abnormal mitochondria.
    Pourmand R; Azzarelli B
    Muscle Nerve; 1994 Oct; 17(10):1218-20. PubMed ID: 7935532
    [No Abstract]   [Full Text] [Related]  

  • 54. A novel ACTA1 mutation causing progressive facioscapuloperoneal myopathy in an adult.
    Kao JC; Liewluck T; Milone M
    J Clin Neurosci; 2018 Jul; 53():261-262. PubMed ID: 29731279
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Congenital myopathy with cap-like structures and nemaline rods: case report and literature review.
    Piteau SJ; Rossiter JP; Smith RG; MacKenzie JJ
    Pediatr Neurol; 2014 Aug; 51(2):192-7. PubMed ID: 25079567
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Myofiber adaptational response to exercise in a mouse model of nemaline myopathy.
    Nair-Shalliker V; Kee AJ; Joya JE; Lucas CA; Hoh JF; Hardeman EC
    Muscle Nerve; 2004 Oct; 30(4):470-80. PubMed ID: 15372535
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1).
    Sewry CA; Holton JL; Dick DJ; Muntoni F; Hanna MG
    Neuromuscul Disord; 2015 May; 25(5):388-91. PubMed ID: 25747004
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Congenital myopathy with cores and nemaline rods in one family].
    Casado JL; Arenas C; Segura D; Chinchón I; González R; Bautista J
    Neurologia; 1995 Mar; 10(3):145-8. PubMed ID: 7756014
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Management of facial dysmorphogenesis in nemaline myopathy: a case report.
    Anderson PJ; Barker JH; David DJ
    World J Orthod; 2005; 6(2):156-60. PubMed ID: 15952552
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Spectrum of congenital myopathies: a single centre experience.
    Uppin MS; Meena AK; Sundaram C
    Neurol India; 2013; 61(3):254-9. PubMed ID: 23860144
    [TBL] [Abstract][Full Text] [Related]  

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