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 *

253 related articles for article (PubMed ID: 9470454)

  • 1. [Cardiac involvement in neuromuscular diseases].
    Posada Rodríguez IJ; Gutiérrez-Rivas E; Cabello A
    Rev Esp Cardiol; 1997 Dec; 50(12):882-901. PubMed ID: 9470454
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiac monitoring and treatment for children and adolescents with neuromuscular disorders.
    English KM; Gibbs JL
    Dev Med Child Neurol; 2006 Mar; 48(3):231-5. PubMed ID: 16483403
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiac manifestations of neuromuscular disorders in children.
    Hsu DT
    Paediatr Respir Rev; 2010 Mar; 11(1):35-8. PubMed ID: 20113990
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cardiac findings in Charcot-Marie-Tooth disease. A prospective study of 68 patients.
    Isner JM; Hawley RJ; Weintraub AM; Engel WK
    Arch Intern Med; 1979 Oct; 139(10):1161-5. PubMed ID: 485749
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.
    Salisachs P
    J Neurol Neurosurg Psychiatry; 1982 Dec; 45(12):1085-91. PubMed ID: 6186770
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Echocardiography in storage and neuromuscular disorders].
    Stöllberger C; Finsterer J
    Wien Klin Wochenschr; 2001 Jun; 113(11-12):408-15. PubMed ID: 11467086
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Congestive cardiomyopathy and pyruvate elevation in a case of Charcot-Marie-Tooth disease].
    Martin-Du Pan RC; Juge C; Perrenoud JJ
    Schweiz Med Wochenschr; 1984 May; 114(18):625-9. PubMed ID: 6539500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers.
    Cetin E; Cuisset JM; Tiffreau V; Vallée L; Hurtevent JF; Thevenon A
    Ann Phys Rehabil Med; 2009; 52(7-8):546-55. PubMed ID: 19713169
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The electrocardiogram: a useful screening test for cardiac involvement in some but not all of the muscular dystrophies.
    Groh WJ
    Heart Rhythm; 2010 Oct; 7(10):1489-90. PubMed ID: 20601147
    [No Abstract]   [Full Text] [Related]  

  • 10. [Ocular disturbances in neuromuscular disorders].
    Pénisson-Besnier I; Lamirel C
    Rev Neurol (Paris); 2008 Nov; 164(11):902-11. PubMed ID: 18808764
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review.
    Arbustini E; Di Toro A; Giuliani L; Favalli V; Narula N; Grasso M
    J Am Coll Cardiol; 2018 Nov; 72(20):2485-2506. PubMed ID: 30442292
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary muscular dystrophies and the heart.
    Hermans MC; Pinto YM; Merkies IS; de Die-Smulders CE; Crijns HJ; Faber CG
    Neuromuscul Disord; 2010 Aug; 20(8):479-92. PubMed ID: 20627570
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nemaline myopathy and cardiomyopathy.
    Skyllouriotis ML; Marx M; Skyllouriotis P; Bittner R; Wimmer M
    Pediatr Neurol; 1999 Apr; 20(4):319-21. PubMed ID: 10328285
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report].
    Chabrak S; Ammar S; Ammar N; Ouali S; Mghaieth F; Larbi N; Kafsi N; Hentati F; Mechmeche R
    Tunis Med; 2006 Jun; 84(6):361-4. PubMed ID: 17042210
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Echocardiographic findings in dystrophia myotonica (Steinert's disease)].
    Sonaglioni G; Curatola L; Bollettini G; Agostini L; Franchetta G; Palestini N; Pignotti M; Floris B
    G Ital Cardiol; 1984 Aug; 14(8):551-6. PubMed ID: 6542038
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cardiomyopathy in hereditary muscular dystrophies].
    Hasselberg NE; Berge KE; Rasmussen M; Früh A; Ørstavik K; Haugaa KH
    Tidsskr Nor Laegeforen; 2018 Jan; 138(1):. PubMed ID: 29313627
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders.
    Sommerville RB; Vincenti MG; Winborn K; Casey A; Stitziel NO; Connolly AM; Mann DL
    Trends Cardiovasc Med; 2017 Jan; 27(1):51-58. PubMed ID: 27452966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The heart in limb girdle muscular dystrophy.
    van der Kooi AJ; de Voogt WG; Barth PG; Busch HF; Jennekens FG; Jongen PJ; de Visser M
    Heart; 1998 Jan; 79(1):73-7. PubMed ID: 9505924
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders].
    Chang XZ; Zhou JY; Yuan Y; Wu Y; Li YX; Zhang W; Jiang YW; Bao XH; Zhang YH; Wang S; Xiong H; Yang YL; Qin J
    Zhonghua Er Ke Za Zhi; 2006 Dec; 44(12):909-12. PubMed ID: 17254458
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.