MacLeod H - Search Results

1

Therapy insight: cardiovascular complications associated with muscular dystrophies.

McNally EM, MacLeod H. McNally EM, et al. Among authors: macleod h. Nat Clin Pract Cardiovasc Med. 2005 Jun;2(6):301-8. doi: 10.1038/ncpcardio0213. Nat Clin Pract Cardiovasc Med. 2005. PMID: 16265534 Review.

2

Lamin A/C truncation in dilated cardiomyopathy with conduction disease.

MacLeod HM, Culley MR, Huber JM, McNally EM. MacLeod HM, et al. BMC Med Genet. 2003 Jul 10;4:4. doi: 10.1186/1471-2350-4-4. BMC Med Genet. 2003. PMID: 12854972 Free PMC article.

3

Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy.

DeWitt MM, MacLeod HM, Soliven B, McNally EM. DeWitt MM, et al. J Am Coll Cardiol. 2006 Oct 3;48(7):1396-8. doi: 10.1016/j.jacc.2006.07.016. Epub 2006 Sep 12. J Am Coll Cardiol. 2006. PMID: 17010801 Free article.

4

A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex.

MacLeod H, Pytel P, Wollmann R, Chelmicka-Schorr E, Silver K, Anderson RB, Waggoner D, McNally EM. MacLeod H, et al. Neuromuscul Disord. 2007 Apr;17(4):285-9. doi: 10.1016/j.nmd.2007.01.005. Epub 2007 Mar 1. Neuromuscul Disord. 2007. PMID: 17336067

5

A pilot study of a family history risk assessment tool for cardiovascular disease.

MacLeod HM, McNally EM. MacLeod HM, et al. J Genet Couns. 2008 Oct;17(5):499-507. doi: 10.1007/s10897-008-9174-z. Epub 2008 Sep 13. J Genet Couns. 2008. PMID: 18791812

6

Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy.

Pytel P, Husain A, Moskowitz I, Raman J, MacLeod H, Anderson AS, Burke M, McNally EM. Pytel P, et al. Among authors: macleod h. Cardiovasc Pathol. 2010 Mar-Apr;19(2):e33-6. doi: 10.1016/j.carpath.2008.09.004. Epub 2008 Nov 21. Cardiovasc Pathol. 2010. PMID: 19026577 Free PMC article.

7

Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.

Mewborn SK, Puckelwartz MJ, Abuisneineh F, Fahrenbach JP, Zhang Y, MacLeod H, Dellefave L, Pytel P, Selig S, Labno CM, Reddy K, Singh H, McNally E. Mewborn SK, et al. Among authors: macleod h. PLoS One. 2010 Dec 14;5(12):e14342. doi: 10.1371/journal.pone.0014342. PLoS One. 2010. PMID: 21179469 Free PMC article.

8

Genetic Counselors' Approach To Postmortem Genetic Testing After Sudden Death: An Exploratory Study.

Liu G, MacLeod H, Webster G, McNally EM, O'Neill SM, Dellefave-Castillo L. Liu G, et al. Among authors: macleod h. Acad Forensic Pathol. 2018 Sep;8(3):738-751. doi: 10.1177/1925362118797748. Epub 2018 Aug 31. Acad Forensic Pathol. 2018. PMID: 31240068 Free PMC article.

9

Family Screening After Sudden Death in a Population-Based Study of Children.

Kannankeril PJ, Shoemaker MB, Fountain D, Roden DM, Yandell M, Tristani-Firouzi M, Etheridge SP, Webster G, George AL, McNally EM, MacLeod H, Burns KM. Kannankeril PJ, et al. Among authors: macleod h. Pediatrics. 2022 Apr 1;149(4):e2021054432. doi: 10.1542/peds.2021-054432. Pediatrics. 2022. PMID: 35284934 Free PMC article.

10

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.

Puckelwartz MJ, Pesce LL, Hernandez EJ, Webster G, Dellefave-Castillo LM, Russell MW, Geisler SS, Kearns SD, Etheridge FK, Etheridge SP, Monroe TO, Pottinger TD, Kannankeril PJ, Shoemaker MB, Fountain D, Roden DM, MacLeod H, Burns KM, Yandell M, Tristani-Firouzi M, George AL, McNally EM. Puckelwartz MJ, et al. Among authors: macleod h. medRxiv [Preprint]. 2023 Mar 29:2023.03.27.23287711. doi: 10.1101/2023.03.27.23287711. medRxiv. 2023. Update in: Genome Med. 2024 Jan 16;16(1):13. doi: 10.1186/s13073-024-01284-w. PMID: 37034657 Free PMC article. Updated. Preprint.

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