Harvard Catalyst Profiles

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Kathryn Swoboda, M.D.

Concepts

This page shows the publications Kathryn Swoboda has written about Muscle, Skeletal.
Connection Strength

1.007
  1. Whole blood survival motor neuron protein levels correlate with severity of denervation in spinal muscular atrophy. Muscle Nerve. 2020 09; 62(3):351-357.
    View in: PubMed
    Score: 0.280
  2. Compound muscle action potential and motor function in children with spinal muscular atrophy. Muscle Nerve. 2010 Nov; 42(5):703-8.
    View in: PubMed
    Score: 0.143
  3. Motor unit number estimation in infants and children with spinal muscular atrophy. Muscle Nerve. 2002 Mar; 25(3):445-7.
    View in: PubMed
    Score: 0.079
  4. Cancer-induced muscle atrophy is determined by intrinsic muscle oxidative capacity. FASEB J. 2021 07; 35(7):e21714.
    View in: PubMed
    Score: 0.075
  5. Exercise training reverses cancer-induced oxidative stress and decrease in muscle COPS2/TRIP15/ALIEN. Mol Metab. 2020 09; 39:101012.
    View in: PubMed
    Score: 0.069
  6. Serum creatinine is a biomarker of progressive denervation in spinal muscular atrophy. Neurology. 2020 03 03; 94(9):e921-e931.
    View in: PubMed
    Score: 0.068
  7. Resistance strength training exercise in children with spinal muscular atrophy. Muscle Nerve. 2015 Oct; 52(4):559-67.
    View in: PubMed
    Score: 0.050
  8. Of SMN in mice and men: a therapeutic opportunity. J Clin Invest. 2011 Aug; 121(8):2978-81.
    View in: PubMed
    Score: 0.038
  9. Perspectives on clinical trials in spinal muscular atrophy. J Child Neurol. 2007 Aug; 22(8):957-66.
    View in: PubMed
    Score: 0.029
  10. An unusual pathologic feature associated with dermatomyositis. Neuromuscul Disord. 2006 Jun; 16(6):391-3.
    View in: PubMed
    Score: 0.026
  11. Natural history of denervation in SMA: relation to age, SMN2 copy number, and function. Ann Neurol. 2005 May; 57(5):704-12.
    View in: PubMed
    Score: 0.024
  12. Counting motor units in chronic motor neuropathies. Exp Neurol. 2003 Nov; 184 Suppl 1:S53-7.
    View in: PubMed
    Score: 0.022
  13. A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies. Eur J Med Genet. 2020 Dec; 63(12):104063.
    View in: PubMed
    Score: 0.018
  14. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat Genet. 1999 Oct; 23(2):208-12.
    View in: PubMed
    Score: 0.017
  15. Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic diet. J Pediatr. 1997 Dec; 131(6):932-4.
    View in: PubMed
    Score: 0.015
  16. Position of glycine substitutions in the triple helix of COL6A1, COL6A2, and COL6A3 is correlated with severity and mode of inheritance in collagen VI myopathies. Hum Mutat. 2013 Nov; 34(11):1558-67.
    View in: PubMed
    Score: 0.011
  17. Clinical and genetic characterization of manifesting carriers of DMD mutations. Neuromuscul Disord. 2010 Aug; 20(8):499-504.
    View in: PubMed
    Score: 0.009
  18. Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Brain. 2009 Feb; 132(Pt 2):452-64.
    View in: PubMed
    Score: 0.008
  19. Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscul Disord. 2008 Jun; 18(6):453-9.
    View in: PubMed
    Score: 0.008
  20. Spinal muscular atrophy: classification, diagnosis, management, pathogenesis, and future research directions. J Child Neurol. 2007 Aug; 22(8):926-45.
    View in: PubMed
    Score: 0.007
  21. Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12. Mol Genet Metab. 2006 Jun; 88(2):138-45.
    View in: PubMed
    Score: 0.007
  22. Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy. Neurology. 2002 Aug 27; 59(4):613-7.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.