Published Manuscripts

  1. Mueller CM, Hilbert JE, Martens WB, Thornton CA, Moxley RT, Greene MH (2009). Hypothesis: neoplasms in myotonic dystrophy. Cancer Causes Control, July 30 [Epub ahead of print].
  2. 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, May 12 [Epub ahead of print].
  3. 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.
  4. 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.
  5. 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.
  6. 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.
  7. 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 10/08/09