Sims KB - Search Results

1

Early diagnosis of peripheral nervous system involvement in Fabry disease and treatment of neuropathic pain: the report of an expert panel.

Burlina AP, Sims KB, Politei JM, Bennett GJ, Baron R, Sommer C, Møller AT, Hilz MJ. Burlina AP, et al. Among authors: sims kb. BMC Neurol. 2011 May 27;11:61. doi: 10.1186/1471-2377-11-61. BMC Neurol. 2011. PMID: 21619592 Free PMC article. Review.

2

Determinants of white matter hyperintensity burden in patients with Fabry disease.

Rost NS, Cloonan L, Kanakis AS, Fitzpatrick KM, Azzariti DR, Clarke V, Lourenco CM, Germain DP, Politei JM, Homola GA, Sommer C, Üçeyler N, Sims KB. Rost NS, et al. Among authors: sims kb. Neurology. 2016 May 17;86(20):1880-6. doi: 10.1212/WNL.0000000000002673. Epub 2016 Apr 20. Neurology. 2016. PMID: 27164662 Free PMC article.

3

Cerebrovascular involvement in Fabry disease: current status of knowledge.

Kolodny E, Fellgiebel A, Hilz MJ, Sims K, Caruso P, Phan TG, Politei J, Manara R, Burlina A. Kolodny E, et al. Stroke. 2015 Jan;46(1):302-13. doi: 10.1161/STROKEAHA.114.006283. Epub 2014 Dec 9. Stroke. 2015. PMID: 25492902 Review. No abstract available.

4

Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: natural history data from the Fabry Registry.

Sims K, Politei J, Banikazemi M, Lee P. Sims K, et al. Stroke. 2009 Mar;40(3):788-94. doi: 10.1161/STROKEAHA.108.526293. Epub 2009 Jan 15. Stroke. 2009. PMID: 19150871

5

Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry.

Watt T, Burlina AP, Cazzorla C, Schönfeld D, Banikazemi M, Hopkin RJ, Martins AM, Sims K, Beitner-Johnson D, O'Brien F, Feldt-Rasmussen U. Watt T, et al. Genet Med. 2010 Nov;12(11):703-12. doi: 10.1097/GIM.0b013e3181f13a4a. Genet Med. 2010. PMID: 20885332 Free article.

6

Fabry disease: guidelines for the evaluation and management of multi-organ system involvement.

Eng CM, Germain DP, Banikazemi M, Warnock DG, Wanner C, Hopkin RJ, Bultas J, Lee P, Sims K, Brodie SE, Pastores GM, Strotmann JM, Wilcox WR. Eng CM, et al. Genet Med. 2006 Sep;8(9):539-48. doi: 10.1097/01.gim.0000237866.70357.c6. Genet Med. 2006. PMID: 16980809 Free article. Review.

7

Understanding the gastrointestinal manifestations of Fabry disease: promoting prompt diagnosis.

Zar-Kessler C, Karaa A, Sims KB, Clarke V, Kuo B. Zar-Kessler C, et al. Among authors: sims kb. Therap Adv Gastroenterol. 2016 Jul;9(4):626-34. doi: 10.1177/1756283X16642936. Epub 2016 Apr 15. Therap Adv Gastroenterol. 2016. PMID: 27366228 Free PMC article. Review.

8

Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors.

Laney DA, Bennett RL, Clarke V, Fox A, Hopkin RJ, Johnson J, O'Rourke E, Sims K, Walter G. Laney DA, et al. J Genet Couns. 2013 Oct;22(5):555-64. doi: 10.1007/s10897-013-9613-3. Epub 2013 Jul 17. J Genet Couns. 2013. PMID: 23860966

9

Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease).

Berkovic SF, Staropoli JF, Carpenter S, Oliver KL, Kmoch S, Anderson GW, Damiano JA, Hildebrand MS, Sims KB, Cotman SL, Bahlo M, Smith KR, Cadieux-Dion M, Cossette P, Jedličková I, Přistoupilová A, Mole SE; ANCL Gene Discovery Consortium. Berkovic SF, et al. Among authors: sims kb. Neurology. 2016 Aug 9;87(6):579-84. doi: 10.1212/WNL.0000000000002943. Epub 2016 Jul 13. Neurology. 2016. PMID: 27412140 Free PMC article.

10

Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry.

Wilcox WR, Oliveira JP, Hopkin RJ, Ortiz A, Banikazemi M, Feldt-Rasmussen U, Sims K, Waldek S, Pastores GM, Lee P, Eng CM, Marodi L, Stanford KE, Breunig F, Wanner C, Warnock DG, Lemay RM, Germain DP; Fabry Registry. Wilcox WR, et al. Mol Genet Metab. 2008 Feb;93(2):112-28. doi: 10.1016/j.ymgme.2007.09.013. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18037317

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