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Journal Abstract Search

337 related items for PubMed ID: 17376125

  • 1. Psychiatric disorders appear equally in patients with myotonic dystrophy, facioscapulohumeral dystrophy, and hereditary motor and sensory neuropathy type I.
    Kalkman JS, Schillings ML, Zwarts MJ, van Engelen BG, Bleijenberg G.
    Acta Neurol Scand; 2007 Apr; 115(4):265-70. PubMed ID: 17376125
    [Abstract] [Full Text] [Related]

  • 2. The development of a model of fatigue in neuromuscular disorders: a longitudinal study.
    Kalkman JS, Schillings ML, Zwarts MJ, van Engelen BG, Bleijenberg G.
    J Psychosom Res; 2007 May; 62(5):571-9. PubMed ID: 17467412
    [Abstract] [Full Text] [Related]

  • 3. Experienced and physiological fatigue in neuromuscular disorders.
    Schillings ML, Kalkman JS, Janssen HM, van Engelen BG, Bleijenberg G, Zwarts MJ.
    Clin Neurophysiol; 2007 Feb; 118(2):292-300. PubMed ID: 17166763
    [Abstract] [Full Text] [Related]

  • 4. Influence of relatives on fatigue experienced by patients with facioscapulohumeral dystrophy, myotonic dystrophy and HMSN-I.
    Kalkman JS, Schillings ML, Zwarts MJ, van Engelen BG, Bleijenberg G.
    Eur Neurol; 2006 Feb; 56(1):24-30. PubMed ID: 16914927
    [Abstract] [Full Text] [Related]

  • 5. Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-I.
    Kalkman JS, Schillings ML, van der Werf SP, Padberg GW, Zwarts MJ, van Engelen BG, Bleijenberg G.
    J Neurol Neurosurg Psychiatry; 2005 Oct; 76(10):1406-9. PubMed ID: 16170086
    [Abstract] [Full Text] [Related]

  • 6. Different types of fatigue in patients with facioscapulohumeral dystrophy, myotonic dystrophy and HMSN-I. Experienced fatigue and physiological fatigue.
    Kalkman JS, Zwarts MJ, Schillings ML, van Engelen BG, Bleijenberg G.
    Neurol Sci; 2008 Sep; 29 Suppl 2():S238-40. PubMed ID: 18690504
    [Abstract] [Full Text] [Related]

  • 7. Temperament and character in patients with classical myotonic dystrophy type 1 (DM-1).
    Winblad S, Lindberg C, Hansen S.
    Neuromuscul Disord; 2005 Apr; 15(4):287-92. PubMed ID: 15792867
    [Abstract] [Full Text] [Related]

  • 8. Quality of life and pain in patients with facioscapulohumeral muscular dystrophy.
    Padua L, Aprile I, Frusciante R, Iannaccone E, Rossi M, Renna R, Messina S, Frasca G, Ricci E.
    Muscle Nerve; 2009 Aug; 40(2):200-5. PubMed ID: 19609906
    [Abstract] [Full Text] [Related]

  • 9. Fatigue and neuromuscular diseases.
    Féasson L, Camdessanché JP, El Mandhi L, Calmels P, Millet GY.
    Ann Readapt Med Phys; 2006 Jul; 49(6):289-300, 375-84. PubMed ID: 16780988
    [Abstract] [Full Text] [Related]

  • 10. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.
    Neurology; 2007 Feb 20; 68(8):569-77. PubMed ID: 17151338
    [Abstract] [Full Text] [Related]

  • 11. Employment status of patients with neuromuscular diseases in relation to personal factors, fatigue and health status: a secondary analysis.
    Minis MA, Kalkman JS, Akkermans RP, Engels JA, Huijbregts PA, Bleijenberg G, Oostendorp RA, van Engelen BG.
    J Rehabil Med; 2010 Jan 20; 42(1):60-5. PubMed ID: 20111846
    [Abstract] [Full Text] [Related]

  • 12. Medication adherence in patients with myotonic dystrophy and facioscapulohumeral muscular dystrophy.
    Fitzgerald BP, Conn KM, Smith J, Walker A, Parkhill AL, Hilbert JE, Luebbe EA, Moxley RT.
    J Neurol; 2016 Dec 20; 263(12):2528-2537. PubMed ID: 27734165
    [Abstract] [Full Text] [Related]

  • 13. Assessement of quadriceps strength, endurance and fatigue in FSHD and CMT: benefits and limits of femoral nerve magnetic stimulation.
    Bachasson D, Temesi J, Bankole C, Lagrange E, Boutte C, Millet GY, Verges S, Levy P, Feasson L, Wuyam B.
    Clin Neurophysiol; 2014 Feb 20; 125(2):396-405. PubMed ID: 24001968
    [Abstract] [Full Text] [Related]

  • 14. The relationship between regional body composition and quantitative strength in facioscapulohumeral muscular dystrophy (FSHD).
    Skalsky AJ, Abresch RT, Han JJ, Shin CS, McDonald CM.
    Neuromuscul Disord; 2008 Nov 20; 18(11):873-80. PubMed ID: 18818077
    [Abstract] [Full Text] [Related]

  • 15. Modafinil reduces fatigue in Charcot-Marie-Tooth disease type 1A: a case series.
    Carter GT, Han JJ, Mayadev A, Weiss MD.
    Am J Hosp Palliat Care; 2006 Nov 20; 23(5):412-6. PubMed ID: 17060310
    [Abstract] [Full Text] [Related]

  • 16. Chronic pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy.
    Jensen MP, Hoffman AJ, Stoelb BL, Abresch RT, Carter GT, McDonald CM.
    Arch Phys Med Rehabil; 2008 Feb 20; 89(2):320-8. PubMed ID: 18226657
    [Abstract] [Full Text] [Related]

  • 17. Severe fatigue and reduced quality of life in children with hereditary motor and sensory neuropathy 1A.
    Jagersma E, Jeukens-Visser M, van Paassen BW, Meester-Delver A, Nollet F.
    J Child Neurol; 2013 Apr 20; 28(4):429-34. PubMed ID: 22752492
    [Abstract] [Full Text] [Related]

  • 18. Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: to lump or split?
    Laberge L, Dauvilliers Y, Bégin P, Richer L, Jean S, Mathieu J.
    Neuromuscul Disord; 2009 Jun 20; 19(6):397-402. PubMed ID: 19403309
    [Abstract] [Full Text] [Related]

  • 19. Neuromuscular electrical stimulation training: a safe and effective treatment for facioscapulohumeral muscular dystrophy patients.
    Colson SS, Benchortane M, Tanant V, Faghan JP, Fournier-Mehouas M, Benaïm C, Desnuelle C, Sacconi S.
    Arch Phys Med Rehabil; 2010 May 20; 91(5):697-702. PubMed ID: 20434605
    [Abstract] [Full Text] [Related]

  • 20. Deterioration of motor function in myotonic dystrophy and hereditary motor and sensory neuropathy.
    Lindeman E, Leffers P, Spaans F, Drukker J, Reulen J.
    Scand J Rehabil Med; 1995 Mar 20; 27(1):59-64. PubMed ID: 7792552
    [Abstract] [Full Text] [Related]

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