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476 results

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Page 1
Medtronic Mosaic porcine bioprosthesis: midterm investigational trial results.
Thomson DJ, Jamieson WR, Dumesnil JG, Burgess JJ, Peniston CM, Métras J, Sullivan JA, Parrott JC, Maitland A, Cybulsky IJ. Thomson DJ, et al. Among authors: sullivan ja. Ann Thorac Surg. 2001 May;71(5 Suppl):S269-72. doi: 10.1016/s0003-4975(01)02551-6. Ann Thorac Surg. 2001. PMID: 11388202 Clinical Trial.
Medtronic intact porcine bioprosthesis: 10 years' experience.
Jamieson WR, Lemieux MD, Sullivan JA, Munro AI, Métras J, Cartier PC. Jamieson WR, et al. Among authors: sullivan ja. Ann Thorac Surg. 1998 Dec;66(6 Suppl):S118-21. doi: 10.1016/s0003-4975(98)01126-6. Ann Thorac Surg. 1998. PMID: 9930430
Medtronic Intact porcine bioprosthesis experience to twelve years.
Jamieson WR, Lemieux MD, Sullivan JA, Munro IA, Métras J, Cartier PC. Jamieson WR, et al. Among authors: sullivan ja. Ann Thorac Surg. 2001 May;71(5 Suppl):S278-81. doi: 10.1016/s0003-4975(01)02548-6. Ann Thorac Surg. 2001. PMID: 11388204
St Jude Medical Epic porcine bioprosthesis: results of the regulatory evaluation.
Jamieson WR, Lewis CT, Sakwa MP, Cooley DA, Kshettry VR, Jones KW, David TE, Sullivan JA, Fradet GJ, Bach DS. Jamieson WR, et al. Among authors: sullivan ja. J Thorac Cardiovasc Surg. 2011 Jun;141(6):1449-54.e2. doi: 10.1016/j.jtcvs.2010.05.055. Epub 2011 Feb 1. J Thorac Cardiovasc Surg. 2011. PMID: 21277603 Free article.
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Barañano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM. Karayol R, et al. Among authors: sullivan ja. Am J Hum Genet. 2024 May 28:S0002-9297(24)00164-2. doi: 10.1016/j.ajhg.2024.05.001. Online ahead of print. Am J Hum Genet. 2024. PMID: 38815585
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Kohler JN, Legro NR, Baldridge D, Shin J, Bowman A, Ugur B, Jackstadt MM, Shriver LP, Patti GJ, Zhang B, Feng W, McAdow AR, Goddard P, Ungar RA, Jensen T, Smith KS, Fresard L, Alvarez R, Bonner D, Reuter CM, McCormack C, Kravets E, Marwaha S, Holt JM; Undiagnosed Diseases Network; Worthey E, Ashley EA, Montgomery SB, Fisher P, Postlethwait J, De Camilli P, Solnica-Krezel L, Bernstein JA, Wheeler MT. Kohler JN, et al. Genet Med. 2024 May 16:101166. doi: 10.1016/j.gim.2024.101166. Online ahead of print. Genet Med. 2024. PMID: 38767059
476 results