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643 results

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Fractures in children with neurofibromatosis type 1 from two NF clinics.
George-Abraham JK, Martin LJ, Kalkwarf HJ, Rieley MB, Stevenson DA, Viskochil DH, Hopkin RJ, Stevens AM, Hanson H, Schorry EK. George-Abraham JK, et al. Among authors: hanson h. Am J Med Genet A. 2013 May;161A(5):921-6. doi: 10.1002/ajmg.a.35541. Epub 2013 Mar 25. Am J Med Genet A. 2013. PMID: 23529831
Multiple increased osteoclast functions in individuals with neurofibromatosis type 1.
Stevenson DA, Yan J, He Y, Li H, Liu Y, Zhang Q, Jing Y, Guo Z, Zhang W, Yang D, Wu X, Hanson H, Li X, Staser K, Viskochil DH, Carey JC, Chen S, Miller L, Roberson K, Moyer-Mileur L, Yu M, Schwarz EL, Pasquali M, Yang FC. Stevenson DA, et al. Among authors: hanson h. Am J Med Genet A. 2011 May;155A(5):1050-9. doi: 10.1002/ajmg.a.33965. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465658 Free PMC article.
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences.
Gripp KW, Sol-Church K, Smpokou P, Graham GE, Stevenson DA, Hanson H, Viskochil DH, Baker LC, Russo B, Gardner N, Stabley DL, Kolbe V, Rosenberger G. Gripp KW, et al. Among authors: hanson h. Am J Med Genet A. 2015 Sep;167A(9):2085-97. doi: 10.1002/ajmg.a.37128. Epub 2015 Apr 25. Am J Med Genet A. 2015. PMID: 25914166 Free PMC article.
Quantitative Ultrasound and Tibial Dysplasia in Neurofibromatosis Type 1.
Stevenson DA, Hanson H, Stevens A, Carey J, Viskochil D, Sheng X, Wheeler K, Slater H. Stevenson DA, et al. Among authors: hanson h. J Clin Densitom. 2018 Apr-Jun;21(2):179-184. doi: 10.1016/j.jocd.2017.03.004. Epub 2017 Apr 21. J Clin Densitom. 2018. PMID: 28438404
Pediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1.
Stevenson DA, Viskochil DH, Carey JC, Sheng X, Murray M, Moyer-Mileur L, Shelton J, Roberts WL, Bunker AM, Hanson H, Bauer S, D'Astous JL. Stevenson DA, et al. Among authors: hanson h. J Pediatr Endocrinol Metab. 2011;24(3-4):169-74. doi: 10.1515/jpem.2011.092. J Pediatr Endocrinol Metab. 2011. PMID: 21648285 Free PMC article.
NF1 Somatic Mutation in Dystrophic Scoliosis.
Margraf RL, VanSant-Webb C, Mao R, Viskochil DH, Carey J, Hanson H, D'Astous J, Grossmann A, Stevenson DA. Margraf RL, et al. Among authors: hanson h. J Mol Neurosci. 2019 May;68(1):11-18. doi: 10.1007/s12031-019-01277-0. Epub 2019 Feb 18. J Mol Neurosci. 2019. PMID: 30778836
Peripheral muscle weakness in RASopathies.
Stevenson DA, Allen S, Tidyman WE, Carey JC, Viskochil DH, Stevens A, Hanson H, Sheng X, Thompson BA, Okumura MJ, Reinker K, Johnson B, Rauen KA. Stevenson DA, et al. Among authors: hanson h. Muscle Nerve. 2012 Sep;46(3):394-9. doi: 10.1002/mus.23324. Muscle Nerve. 2012. PMID: 22907230
643 results