Heckmann JM - Search Results

1

A functional SNP in the regulatory region of the decay-accelerating factor gene associates with extraocular muscle pareses in myasthenia gravis.

Heckmann JM, Uwimpuhwe H, Ballo R, Kaur M, Bajic VB, Prince S. Heckmann JM, et al. Genes Immun. 2010 Jan;11(1):1-10. doi: 10.1038/gene.2009.61. Epub 2009 Aug 13. Genes Immun. 2010. PMID: 19675582 Free PMC article.

2

Myasthenia gravis in South Africans: racial differences in clinical manifestations.

Heckmann JM, Owen EP, Little F. Heckmann JM, et al. Neuromuscul Disord. 2007 Dec;17(11-12):929-34. doi: 10.1016/j.nmd.2007.07.002. Epub 2007 Aug 27. Neuromuscul Disord. 2007. PMID: 17720497

3

Association of transforming growth factor β-1 (TGFB1) regulatory region polymorphisms with myasthenia gravis-related ophthalmoparesis.

Akinyi MV, Dandara C, Gamieldien J, Heckmann JM. Akinyi MV, et al. Among authors: heckmann jm. J Neuroimmunol. 2012 May 15;246(1-2):96-9. doi: 10.1016/j.jneuroim.2012.03.002. Epub 2012 Mar 27. J Neuroimmunol. 2012. PMID: 22458981 Retracted.

4

The effects of prednisone and steroid-sparing agents on decay accelerating factor (CD55) expression: implications in myasthenia gravis.

Auret J, Abrahams A, Prince S, Heckmann JM. Auret J, et al. Among authors: heckmann jm. Neuromuscul Disord. 2014 Jun;24(6):499-508. doi: 10.1016/j.nmd.2014.02.010. Epub 2014 Mar 6. Neuromuscul Disord. 2014. PMID: 24703255

5

The African-387 C>T TGFB1 variant is functional and associates with the ophthalmoplegic complication in juvenile myasthenia gravis.

Nel M, Buys JM, Rautenbach R, Mowla S, Prince S, Heckmann JM. Nel M, et al. Among authors: heckmann jm. J Hum Genet. 2016 Apr;61(4):307-16. doi: 10.1038/jhg.2015.146. Epub 2015 Dec 3. J Hum Genet. 2016. PMID: 26632886

6

Randomized Trial of Thymectomy in Myasthenia Gravis.

Wolfe GI, Kaminski HJ, Aban IB, Minisman G, Kuo HC, Marx A, Ströbel P, Mazia C, Oger J, Cea JG, Heckmann JM, Evoli A, Nix W, Ciafaloni E, Antonini G, Witoonpanich R, King JO, Beydoun SR, Chalk CH, Barboi AC, Amato AA, Shaibani AI, Katirji B, Lecky BR, Buckley C, Vincent A, Dias-Tosta E, Yoshikawa H, Waddington-Cruz M, Pulley MT, Rivner MH, Kostera-Pruszczyk A, Pascuzzi RM, Jackson CE, Garcia Ramos GS, Verschuuren JJ, Massey JM, Kissel JT, Werneck LC, Benatar M, Barohn RJ, Tandan R, Mozaffar T, Conwit R, Odenkirchen J, Sonett JR, Jaretzki A 3rd, Newsom-Davis J, Cutter GR; MGTX Study Group. Wolfe GI, et al. Among authors: heckmann jm. N Engl J Med. 2016 Aug 11;375(6):511-22. doi: 10.1056/NEJMoa1602489. N Engl J Med. 2016. PMID: 27509100 Free PMC article. Clinical Trial.

7

Extraocular Muscle Findings in Myasthenia Gravis Associated Treatment-Resistant Ophthalmoplegia.

Rautenbach RM, Pillay K, Murray ADN, Heckmann JM. Rautenbach RM, et al. Among authors: heckmann jm. J Neuroophthalmol. 2017 Dec;37(4):414-417. doi: 10.1097/WNO.0000000000000534. J Neuroophthalmol. 2017. PMID: 28742638

8

A unique subphenotype of myasthenia gravis.

Heckmann JM, Nel M. Heckmann JM, et al. Ann N Y Acad Sci. 2018 Jan;1412(1):14-20. doi: 10.1111/nyas.13471. Epub 2017 Oct 6. Ann N Y Acad Sci. 2018. PMID: 28984362 Review.

9

The functionality of African-specific variants in the TGFB1 regulatory region and their potential role in HIVAN.

Nel M, Buys JM, Botha FCJ, Wearne N, Prince S, Heckmann JM. Nel M, et al. Among authors: heckmann jm. Clin Exp Nephrol. 2018 Aug;22(4):764-772. doi: 10.1007/s10157-017-1516-4. Epub 2017 Dec 4. Clin Exp Nephrol. 2018. PMID: 29204904

10

Profiling of patient-specific myocytes identifies altered gene expression in the ophthalmoplegic subphenotype of myasthenia gravis.

Nel M, Prince S, Heckmann JM. Nel M, et al. Among authors: heckmann jm. Orphanet J Rare Dis. 2019 Jan 29;14(1):24. doi: 10.1186/s13023-019-1003-y. Orphanet J Rare Dis. 2019. PMID: 30696470 Free PMC article.

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