Published Manuscripts

  1. Nieto R, Raichle KA, Jensen MP, Miró J (2011). Changes in pain-related beliefs, coping, and catastrophizing predict changes in pain intensity, pain interference, and psychological functioning in individuals with myotonic muscular dystrophy and facioscapulohumeral muscular dystrophy. Clin J Pain, Jun 2. [Epub ahead of print]
  2. Heatwole C.R., Eichinger K.J., Friedman D.I., Hilbert J.E., Jackson C.E., Logigian E.L., Martens W.B., McDermott M.P., Pandya S.K., Quinn C., Smirnow A.M., Thornton C.A., Moxley R.T. 3rd. (2010). Open-Label Trial of Recombinant Human Insulin-like Growth Factor 1/Recombinant Human Insulin-like Growth Factor Binding Protein 3 in Myotonic Dystrophy Type 1. Arch Neurol. 2011 Jan;68(1):37-44. Epub 2010 Sep 13.
  3. Prendergast P, Magalhaes S, Campbell C. (2010). Congenital myotonic dystrophy in a national registry. Paediatr Child Health. 2010 Oct; 15(8):514-8.
  4. Mueller CM, Hilbert JE, Martens WB, Thornton CA, Moxley RT, Greene MH (2009). Hypothesis: neoplasms in myotonic dystrophy. Cancer Causes Control, 20(10):2009-2020.
  5. Miro J, Raichle KA, Carter GT, O'Brien SA, Abresch RT, McDonald CM, Jensen MP (2009). Impact of biopsychosocial factors on chronic pain in persons with myotonic and facioscapulohumeral muscular dystrophy. Am J Hosp Palliat Care, 26(4):308-319.
  6. Ciafaloni E, Mignot E, Sansone V, Hilbert JE, Lin L, Lin X, Liu LC, Pigeon WR, Perlis ML, Thornton CA (2008). The hypocretin neurotransmission system in myotonic dystrophy type 1. Neurology, 70(3):226-230.
  7. Jensen MP, Hoffman AJ, Stoelb BL, Abresch RT, Carter GT, McDonald CM (2008). Chronic pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy. Arch Phys Med Rehabil, 89(2):320-8.
  8. Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R (2006). Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology, 68:569-577.
  9. Ciafaloni E, Pressman EK, Loi AM, Smirnow AM, Guntrum DJ, Dilek N, Tawil R (2006). Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophy. Neurology, 67(10):1887-9.
  10. Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA (2006). Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy. Human Molecular Genetics, 15(13):2087-2097.

 

Last Reviewed and Updated 10/18/11