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Page 1
Showing results for spahr a
Search for Spaur A instead (1 results)
MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr type.
Bonafé L, Liang J, Gorna MW, Zhang Q, Ha-Vinh R, Campos-Xavier AB, Unger S, Beckmann JS, Le Béchec A, Stevenson B, Giedion A, Liu X, Superti-Furga G, Wang W, Spahr A, Superti-Furga A. Bonafé L, et al. Among authors: spahr a. Am J Med Genet A. 2014 May;164A(5):1175-9. doi: 10.1002/ajmg.a.36431. Epub 2014 Mar 19. Am J Med Genet A. 2014. PMID: 24648384
Transcatheter Aortic Valve Replacement Patient Care Improvements; It Takes a Team.
Keegan PA, Mitchell R, Stoneman C, Arrington WS, Spahr A, Brown T, Biven K, Donovan E, Kalinke L, Mathew P, Harrison M, Jones E, Higgins M, Hester K, Gaston J, Mortorano C. Keegan PA, et al. Among authors: spahr a. Crit Care Nurs Clin North Am. 2022 Jun;34(2):205-214. doi: 10.1016/j.cnc.2022.02.008. Epub 2022 Apr 28. Crit Care Nurs Clin North Am. 2022. PMID: 35660234 Review.
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study.
Yazdani PA, St-Jean ML, Matovic S, Spahr A, Tran LT, Boucher RM, Poulin C, Osterman B, Srour M, Rosenblatt B, Chénier S, Soucy JF, Laberge AM, D'Agostino MD, Nguyen CE, Morsa M, Bernard G. Yazdani PA, et al. Among authors: spahr a. J Child Neurol. 2023 Apr;38(5):329-335. doi: 10.1177/08830738231176672. Epub 2023 May 24. J Child Neurol. 2023. PMID: 37225698 Free PMC article.
Authors' response.
Patterson BM, Dalci O, Papadopoulou AK, Madukuri S, Mahon J, Petocz P, Spahr A, Darendeliler MA. Patterson BM, et al. Among authors: spahr a. Am J Orthod Dentofacial Orthop. 2017 Jul;152(1):12-13. doi: 10.1016/j.ajodo.2017.04.015. Am J Orthod Dentofacial Orthop. 2017. PMID: 28651758 No abstract available.
116 results