Harvard Catalyst Profiles

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Kathryn Swoboda, M.D.

Concepts

This page shows the publications Kathryn Swoboda has written about Spinal Muscular Atrophies of Childhood.
  1. Whole-blood dysregulation of actin-cytoskeleton pathway in adult spinal muscular atrophy patients. Ann Clin Transl Neurol. 2020 07; 7(7):1158-1165.
    View in: PubMed
    Score: 0.801
  2. Responses to Fasting and Glucose Loading in a Cohort of Well Children with Spinal Muscular Atrophy Type II. J Pediatr. 2015 Dec; 167(6):1362-8.e1.
    View in: PubMed
    Score: 0.579
  3. Nutritional practices at a glance: spinal muscular atrophy type I nutrition survey findings. J Child Neurol. 2014 Nov; 29(11):1467-72.
    View in: PubMed
    Score: 0.504
  4. Vitamin D intake is inadequate in spinal muscular atrophy type I cohort: correlations with bone health. J Child Neurol. 2014 Mar; 29(3):374-80.
    View in: PubMed
    Score: 0.479
  5. Observational study of caloric and nutrient intake, bone density, and body composition in infants and children with spinal muscular atrophy type I. Neuromuscul Disord. 2012 Nov; 22(11):966-73.
    View in: PubMed
    Score: 0.463
  6. 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: 0.411
  7. Vascular perfusion abnormalities in infants with spinal muscular atrophy. J Pediatr. 2009 Aug; 155(2):292-4.
    View in: PubMed
    Score: 0.377
  8. Perspectives on clinical trials in spinal muscular atrophy. J Child Neurol. 2007 Aug; 22(8):957-66.
    View in: PubMed
    Score: 0.328
  9. Spinal muscular atrophy genetic counseling access and genetic knowledge: parents' perspectives. J Child Neurol. 2007 Aug; 22(8):1019-26.
    View in: PubMed
    Score: 0.328
  10. A modified Hammersmith functional motor scale for use in multi-center research on spinal muscular atrophy. Neuromuscul Disord. 2006 Jul; 16(7):417-26.
    View in: PubMed
    Score: 0.303
  11. Motor unit number estimation in infants and children with spinal muscular atrophy. Muscle Nerve. 2002 Mar; 25(3):445-7.
    View in: PubMed
    Score: 0.225
  12. Stander Use in Spinal Muscular Atrophy: Results From a Large Natural History Database. Pediatr Phys Ther. 2020 07; 32(3):235-241.
    View in: PubMed
    Score: 0.201
  13. Nusinersen in later-onset spinal muscular atrophy: Long-term results from the phase 1/2 studies. Neurology. 2019 05 21; 92(21):e2492-e2506.
    View in: PubMed
    Score: 0.185
  14. Natural history of infantile-onset spinal muscular atrophy. Ann Neurol. 2017 Dec; 82(6):883-891.
    View in: PubMed
    Score: 0.168
  15. Clinical trial of L-Carnitine and valproic acid in spinal muscular atrophy type I. Muscle Nerve. 2018 02; 57(2):193-199.
    View in: PubMed
    Score: 0.166
  16. Reliability and validity of the TIMPSI for infants with spinal muscular atrophy type I. Pediatr Phys Ther. 2013; 25(2):140-8; discussion 149.
    View in: PubMed
    Score: 0.119
  17. Glucose metabolism and pancreatic defects in spinal muscular atrophy. Ann Neurol. 2012 Aug; 72(2):256-68.
    View in: PubMed
    Score: 0.116
  18. Spinal muscular atrophy type 1: are proactive respiratory interventions associated with longer survival? Pediatr Crit Care Med. 2012 May; 13(3):e161-5.
    View in: PubMed
    Score: 0.114
  19. Reliability of the Modified Hammersmith Functional Motor Scale in young children with spinal muscular atrophy. Muscle Nerve. 2011 Aug; 44(2):246-51.
    View in: PubMed
    Score: 0.107
  20. The Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): test development and reliability. Neuromuscul Disord. 2010 Mar; 20(3):155-61.
    View in: PubMed
    Score: 0.097
  21. Spinal muscular atrophy: classification, diagnosis, management, pathogenesis, and future research directions. J Child Neurol. 2007 Aug; 22(8):926-45.
    View in: PubMed
    Score: 0.082
  22. Congenital bone fractures in spinal muscular atrophy: functional role for SMN protein in bone remodeling. J Child Neurol. 2007 Aug; 22(8):967-73.
    View in: PubMed
    Score: 0.082
  23. Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2. . 2004 Oct 15; 130A(3):307-10.
    View in: PubMed
    Score: 0.068
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.