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 *

144 related articles for article (PubMed ID: 11467086)

  • 1. [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]  

  • 2. [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]  

  • 3. Use of tissue Doppler imaging to identify and manage systemic diseases.
    Weidemann F; Strotmann JM
    Clin Res Cardiol; 2008 Feb; 97(2):65-73. PubMed ID: 17713717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical aspects of left ventricular diastolic function assessed by Doppler echocardiography following acute myocardial infarction.
    Poulsen SH
    Dan Med Bull; 2001 Nov; 48(4):199-210. PubMed ID: 11767125
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Cardiac involvement in myotonic muscular dystrophy.
    Moorman JR; Coleman RE; Packer DL; Kisslo JA; Bell J; Hettleman BD; Stajich J; Roses AD
    Medicine (Baltimore); 1985 Nov; 64(6):371-87. PubMed ID: 4058303
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cardiac manifestations of Becker-type muscular dystrophy.
    Vrints C; Mercelis R; Vanagt E; Snoeck J; Martin JJ
    Acta Cardiol; 1983; 38(5):479-86. PubMed ID: 6606925
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Echocardiographic findings in some metabolic storage diseases.
    Senocak F; Sarçlar M; Ozkutlu S
    Jpn Heart J; 1994 Sep; 35(5):635-43. PubMed ID: 7830328
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiorespiratory function in Duchenne and Becker muscular dystrophy.
    Taşdemir HA; Cil E; Topaloğlu H; Yalaz K; Aysun S; Renda Y; Ozme S
    Turk J Pediatr; 1996; 38(3):307-14. PubMed ID: 8827899
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Left ventricular function in adults with muscular dystrophies: genotype-phenotype correlations.
    Martins E; Silva-Cardoso J; Silveira F; Nadais G; Gonçalves FR
    Rev Port Cardiol; 2005 Jan; 24(1):23-35. PubMed ID: 15773664
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amyloidosis and cardiac involvement.
    Cacoub P; Axler O; De Zuttere D; Hausfater P; Amoura Z; Walter S; Wechsler B; Godeau P; Piette JC
    Ann Med Interne (Paris); 2000 Dec; 151(8):611-7. PubMed ID: 11173703
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondriopathy: a rare aetiology of restrictive cardiomyopathy.
    Thebault C; Ollivier R; Leurent G; Marcorelles P; Langella B; Donal E
    Eur J Echocardiogr; 2008 Nov; 9(6):840-5. PubMed ID: 18579503
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy.
    Esposito G; Ruggiero R; Savarese M; Savarese G; Tremolaterra MR; Salvatore F; Carsana A
    Clin Chem Lab Med; 2013 Dec; 51(12):2239-45. PubMed ID: 23729582
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Myocardial diseases].
    Tanaka H
    Nihon Naika Gakkai Zasshi; 1999 Sep; 88(9):1630-44. PubMed ID: 10581742
    [No Abstract]   [Full Text] [Related]  

  • 17. A comparison between MUGA and echocardiography in patients with muscular dystrophy in the early detection of cardiac involvement.
    Oğuz D; Olguntürk R; Gücüyener K; Açikgöz GV; Tunaoğlu FS
    Pediatr Cardiol; 1998; 19(2):150-4. PubMed ID: 9565507
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Evaluation of cranial CT findings of patients with muscular dystrophy: with a reference to cerebral vascular disease and cardiac complications].
    Konagaya M; Sakai M; Kuru S; Kato T; Yasuma F; Matsuoka Y
    No To Shinkei; 1999 Jul; 51(7):621-6. PubMed ID: 10457950
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Echocardiographic features of genetic diseases: part 2. Storage disease.
    Alizad A; Seward JB
    J Am Soc Echocardiogr; 2000 Feb; 13(2):164-70. PubMed ID: 10668023
    [No Abstract]   [Full Text] [Related]  

  • 20. Deposit Diseases as Differential Diagnosis of Left Ventricular Hypertrophy in Patients with Heart Failure and Preserved Systolic Function.
    Fernandes F; Antunes MO; Hotta VT; Rochitte CE; Mady C
    Arq Bras Cardiol; 2019 Nov; 113(5):979-987. PubMed ID: 31800724
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.