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Items: 1 to 50 of 283

1.

FBN1 Coding Variants and Nonsyndromic Aortic Disease.

Damrauer SM, Hardie K, Kember RL, Judy R, Birtwell D, Williams H, Rader DJ, Pyeritz RE.

Circ Genom Precis Med. 2019 Jun;12(6):e002454. doi: 10.1161/CIRCGEN.119.002454. Epub 2019 Jun 18. No abstract available.

PMID:
31211626
2.

Response to Knoppers et al.

David KL, Best RG, Brenman LM, Bush L, Deignan J, Flannery D, Hoffman JD, Holm I, Miller DT, O'Leary J, Pyeritz RE.

Genet Med. 2019 Apr 11. doi: 10.1038/s41436-019-0496-z. [Epub ahead of print] No abstract available.

PMID:
30971833
3.

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).

David KL, Best RG, Brenman LM, Bush L, Deignan JL, Flannery D, Hoffman JD, Holm I, Miller DT, O'Leary J, Pyeritz RE; ACMG Social Ethical Legal Issues Committee.

Genet Med. 2019 Apr;21(4):769-771. doi: 10.1038/s41436-018-0391-z. Epub 2018 Dec 22. No abstract available.

PMID:
30578420
4.

Marfan syndrome: improved clinical history results in expanded natural history.

Pyeritz RE.

Genet Med. 2018 Dec 21. doi: 10.1038/s41436-018-0399-4. [Epub ahead of print] Review.

PMID:
30573797
5.

Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome.

Handisides JC, Hollenbeck-Pringle D, Uzark K, Trachtenberg FL, Pemberton VL, Atz TW, Bradley TJ, Cappella E, De Nobele S, Groh GK, Hamstra MS, Korsin R, Levine JC, Lindauer B, Liou A, Neal MKM, Markham LW, Morrison T, Mussatto KA, Olson AK, Pierpont MEM, Pyeritz RE, Radojewski EA, Roman MJ, Xu M, Lacro RV; Pediatric Heart Network Investigators.

J Pediatr. 2019 Jan;204:250-255.e1. doi: 10.1016/j.jpeds.2018.08.061. Epub 2018 Sep 27.

PMID:
30270167
6.

Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia.

Wooderchak-Donahue WL, McDonald J, Farrell A, Akay G, Velinder M, Johnson P, VanSant-Webb C, Margraf R, Briggs E, Whitehead KJ, Thomson J, Lin AE, Pyeritz RE, Marth G, Bayrak-Toydemir P.

J Med Genet. 2018 Dec;55(12):824-830. doi: 10.1136/jmedgenet-2018-105561. Epub 2018 Sep 22.

PMID:
30244195
7.

Comparison of Outcomes in DeBakey Type AI Versus AII Aortic Dissection.

Kohl LP, Isselbacher EM, Majahalme N, Evangelista A, Russo MJ, Hutchison S, Bossone E, Suzuki T, Pyeritz RE, Gleason TG, Conklin LD, Montgomery DG, Nienaber CA, Eagle KA, Harris KM.

Am J Cardiol. 2018 Aug 15;122(4):689-695. doi: 10.1016/j.amjcard.2018.04.042. Epub 2018 Jun 30.

PMID:
29970240
8.

Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome.

Hoskoppal A, Menon S, Trachtenberg F, Burns KM, De Backer J, Gelb BD, Gleason M, James J, Lai WW, Liou A, Mahony L, Olson AK, Pyeritz RE, Sharkey AM, Stylianou M, Wechsler SB, Young L, Levine JC, Tierney ESS, Lacro RV, Bradley TJ; Pediatric Heart Network Investigators.

Pediatr Cardiol. 2018 Oct;39(7):1453-1461. doi: 10.1007/s00246-018-1916-6. Epub 2018 Jun 11.

9.

Covered Stents in the Treatment of Pulmonary Arteriovenous Malformations.

Bai HX, Pyeritz RE, Trerotola SO.

J Vasc Interv Radiol. 2018 Jul;29(7):981-985. doi: 10.1016/j.jvir.2017.12.024.

PMID:
29935788
10.

Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome.

Selamet Tierney ES, Levine JC, Sleeper LA, Roman MJ, Bradley TJ, Colan SD, Chen S, Campbell MJ, Cohen MS, De Backer J, Heydarian H, Hoskoppal A, Lai WW, Liou A, Marcus E, Nutting A, Olson AK, Parra DA, Pearson GD, Pierpont ME, Printz BF, Pyeritz RE, Ravekes W, Sharkey AM, Srivastava S, Young L, Lacro RV; Pediatric Heart Network Investigators.

Am J Cardiol. 2018 May 1;121(9):1094-1101. doi: 10.1016/j.amjcard.2018.01.016. Epub 2018 Feb 13.

11.

Etiology and pathogenesis of the Marfan syndrome: current understanding.

Pyeritz RE.

Ann Cardiothorac Surg. 2017 Nov;6(6):595-598. doi: 10.21037/acs.2017.10.04. Review.

12.

Chronobiology of Acute Aortic Syndromes.

Siddiqi HK, Bossone E, Pyeritz RE, Eagle KA.

Heart Fail Clin. 2017 Oct;13(4):697-701. doi: 10.1016/j.hfc.2017.05.006. Epub 2017 Jul 11. Review.

PMID:
28865779
13.

Bicuspid and unicuspid aortic valves: Different phenotypes of the same disease? Insight from the GenTAC Registry.

Krepp JM, Roman MJ, Devereux RB, Bruce A, Prakash SK, Morris SA, Milewicz DM, Holmes KW, Ravekes W, Shohet RV, Pyeritz RE, Maslen CL, Kroner BL, Eagle KA, Preiss L; GenTAC Investigators, Asch FM.

Congenit Heart Dis. 2017 Dec;12(6):740-745. doi: 10.1111/chd.12520. Epub 2017 Aug 14.

14.

Aortic Dilatation Associated With Bicuspid Aortic Valve: Relation to Sex, Hemodynamics, and Valve Morphology (the National Heart Lung and Blood Institute-Sponsored National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions).

Roman MJ, Pugh NL, Devereux RB, Eagle KA, Holmes K, LeMaire SA, Milewski RK, Morris SA, Prakash SK, Pyeritz RE, Ravekes WJ, Shohet RV, Song HK, Asch FM; GenTAC Investigators.

Am J Cardiol. 2017 Oct 1;120(7):1171-1175. doi: 10.1016/j.amjcard.2017.06.061. Epub 2017 Jul 14.

15.

Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.

Amyere M, Revencu N, Helaers R, Pairet E, Baselga E, Cordisco M, Chung W, Dubois J, Lacour JP, Martorell L, Mazereeuw-Hautier J, Pyeritz RE, Amor DJ, Bisdorff A, Blei F, Bombei H, Dompmartin A, Brooks D, Dupont J, González-Enseñat MA, Frieden I, Gérard M, Kvarnung M, Hanson-Kahn AK, Hudgins L, Léauté-Labrèze C, McCuaig C, Metry D, Parent P, Paul C, Petit F, Phan A, Quere I, Salhi A, Turner A, Vabres P, Vicente A, Wargon O, Watanabe S, Weibel L, Wilson A, Willing M, Mulliken JB, Boon LM, Vikkula M.

Circulation. 2017 Sep 12;136(11):1037-1048. doi: 10.1161/CIRCULATIONAHA.116.026886. Epub 2017 Jul 7.

PMID:
28687708
16.

Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry.

Roman MJ, Devereux RB, Preiss LR, Asch FM, Eagle KA, Holmes KW, LeMaire SA, Maslen CL, Milewicz DM, Morris SA, Prakash SK, Pyeritz RE, Ravekes WJ, Shohet RV, Song HK, Weinsaft JW; GenTAC Investigators*.

Circ Cardiovasc Genet. 2017 Jun;10(3). pii: e001647. doi: 10.1161/CIRCGENETICS.116.001647.

17.

A Survey of Pulmonary Arteriovenous Malformation Screening, Management, and Follow-Up in Hereditary Hemorrhagic Telangiectasia Centers of Excellence.

Chick JFB, Reddy SN, Pyeritz RE, Trerotola SO.

Cardiovasc Intervent Radiol. 2017 Jul;40(7):1003-1009. doi: 10.1007/s00270-017-1604-6. Epub 2017 Feb 10.

PMID:
28188364
18.

Hereditary Hemorrhagic Telangiectasia.

McDonald J, Pyeritz RE.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2000 Jun 26 [updated 2017 Feb 2].

19.

Chronobiology of Acute Aortic Dissection in the Marfan Syndrome (from the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions and the International Registry of Acute Aortic Dissection).

Siddiqi HK, Luminais SN, Montgomery D, Bossone E, Dietz H, Evangelista A, Isselbacher E, LeMaire S, Manfredini R, Milewicz D, Nienaber CA, Roman M, Sechtem U, Silberbach M, Eagle KA, Pyeritz RE; GenTAC and IRAD investigators.

Am J Cardiol. 2017 Mar 1;119(5):785-789. doi: 10.1016/j.amjcard.2016.11.021. Epub 2016 Dec 2.

PMID:
28065489
20.

The role of the multidisciplinary health care team in the management of patients with Marfan syndrome.

von Kodolitsch Y, Rybczynski M, Vogler M, Mir TS, Schüler H, Kutsche K, Rosenberger G, Detter C, Bernhardt AM, Larena-Avellaneda A, Kölbel T, Debus ES, Schroeder M, Linke SJ, Fuisting B, Napp B, Kammal AL, Püschel K, Bannas P, Hoffmann BA, Gessler N, Vahle-Hinz E, Kahl-Nieke B, Thomalla G, Weiler-Normann C, Ohm G, Neumann S, Benninghoven D, Blankenberg S, Pyeritz RE.

J Multidiscip Healthc. 2016 Nov 3;9:587-614. eCollection 2016. Review.

21.

Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia: A Randomized Clinical Trial.

Whitehead KJ, Sautter NB, McWilliams JP, Chakinala MM, Merlo CA, Johnson MH, James M, Everett EM, Clancy MS, Faughnan ME, Oh SP, Olitsky SE, Pyeritz RE, Gossage JR.

JAMA. 2016 Sep 6;316(9):943-51. doi: 10.1001/jama.2016.11724.

PMID:
27599329
22.

Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).

Roman MJ, Pugh NL, Hendershot TP, Devereux RB, Dietz H, Holmes K, Eagle KA, LeMaire SA, Milewicz DM, Morris SA, Pyeritz RE, Ravekes WJ, Shohet RV, Silberbach M; GenTAC InvestigatorsDietzHarry C.HabashiJenniferPrakashSiddharth K.MaslenCheryl L.SongHoward K.BavariaJoseph E.MilewskiKariannaWeinsaftJonathan W.McDonnellNazliAschFederico M.TolunayH. EserDesvigne‐NickensPatriceTsengHungKronerBarbara L.

J Am Heart Assoc. 2016 Aug 11;5(8). pii: e004052. doi: 10.1161/JAHA.116.004052.

23.

Aortic Dissection in Patients With Genetically Mediated Aneurysms: Incidence and Predictors in the GenTAC Registry.

Weinsaft JW, Devereux RB, Preiss LR, Feher A, Roman MJ, Basson CT, Geevarghese A, Ravekes W, Dietz HC, Holmes K, Habashi J, Pyeritz RE, Bavaria J, Milewski K, LeMaire SA, Morris S, Milewicz DM, Prakash S, Maslen C, Song HK, Silberbach GM, Shohet RV, McDonnell N, Hendershot T, Eagle KA, Asch FM; GENTAC Registry Investigators.

J Am Coll Cardiol. 2016 Jun 14;67(23):2744-2754. doi: 10.1016/j.jacc.2016.03.570.

24.

Shock complicating type A acute aortic dissection: Clinical correlates, management, and outcomes.

Bossone E, Pyeritz RE, Braverman AC, Peterson MD, Ehrlich M, O'Gara P, Suzuki T, Trimarchi S, Gilon D, Greason K, Desai ND, Montgomery DG, Isselbacher EM, Nienaber CA, Eagle KA; IRAD Investigators.

Am Heart J. 2016 Jun;176:93-9. doi: 10.1016/j.ahj.2016.02.019. Epub 2016 Mar 17.

PMID:
27264225
25.

Recent progress in understanding the natural and clinical histories of the Marfan syndrome.

Pyeritz RE.

Trends Cardiovasc Med. 2016 Jul;26(5):423-8. doi: 10.1016/j.tcm.2015.12.003. Epub 2016 Jan 13. Review.

PMID:
26908026
26.

The Expanding Clinical Spectrum of Extracardiovascular and Cardiovascular Manifestations of Heritable Thoracic Aortic Aneurysm and Dissection.

Bradley TJ, Bowdin SC, Morel CF, Pyeritz RE.

Can J Cardiol. 2016 Jan;32(1):86-99. doi: 10.1016/j.cjca.2015.11.007. Epub 2015 Nov 14. Review.

PMID:
26724513
27.

Gene-environment interactions.

Pyeritz RE.

Genet Med. 2015 Nov;17(11):943-5. doi: 10.1038/gim.2015.126. Epub 2015 Sep 10. No abstract available.

PMID:
26355661
28.

Atenolol versus losartan in children and young adults with Marfan's syndrome.

Lacro RV, Dietz HC, Sleeper LA, Yetman AT, Bradley TJ, Colan SD, Pearson GD, Selamet Tierney ES, Levine JC, Atz AM, Benson DW, Braverman AC, Chen S, De Backer J, Gelb BD, Grossfeld PD, Klein GL, Lai WW, Liou A, Loeys BL, Markham LW, Olson AK, Paridon SM, Pemberton VL, Pierpont ME, Pyeritz RE, Radojewski E, Roman MJ, Sharkey AM, Stylianou MP, Wechsler SB, Young LT, Mahony L; Pediatric Heart Network Investigators.

N Engl J Med. 2014 Nov 27;371(22):2061-71. doi: 10.1056/NEJMoa1404731. Epub 2014 Nov 18.

29.

What is the optimal medical therapy for Marfan syndrome?

Pyeritz RE.

J Pediatr. 2014 Nov;165(5):889-90. doi: 10.1016/j.jpeds.2014.08.002. Epub 2014 Sep 11. No abstract available.

PMID:
25217843
30.

Cocaine-related aortic dissection: lessons from the International Registry of Acute Aortic Dissection.

Dean JH, Woznicki EM, O'Gara P, Montgomery DG, Trimarchi S, Myrmel T, Pyeritz RE, Harris KM, Suzuki T, Braverman AC, Hughes GC, Kline-Rogers E, Nienaber CA, Isselbacher EM, Eagle KA, Bossone E.

Am J Med. 2014 Sep;127(9):878-85. doi: 10.1016/j.amjmed.2014.05.005. Epub 2014 May 14.

PMID:
24835037
31.

Pulse pressure and type A acute aortic dissection in-hospital outcomes (from the International Registry of Acute Aortic Dissection).

Hoff E, Eagle T, Pyeritz RE, Ehrlich M, Voehringer M, Bossone E, Hutchison S, Peterson MD, Suzuki T, Greason K, Forteza A, Montgomery DG, Isselbacher EM, Nienaber CA, Eagle KA.

Am J Cardiol. 2014 Apr 1;113(7):1255-9. doi: 10.1016/j.amjcard.2013.12.037. Epub 2014 Jan 15.

PMID:
24521716
32.

"Use it or lose it" as an alternative approach to protect genetic privacy in personalized medicine.

Wagner JK, Mozersky JT, Pyeritz RE.

Urol Oncol. 2014 Feb;32(2):198-201. doi: 10.1016/j.urolonc.2013.09.016. No abstract available.

33.

Heritable thoracic aortic disorders.

Pyeritz RE.

Curr Opin Cardiol. 2014 Jan;29(1):97-102. doi: 10.1097/HCO.0000000000000023. Review.

PMID:
24284977
34.

Stroke and outcomes in patients with acute type A aortic dissection.

Bossone E, Corteville DC, Harris KM, Suzuki T, Fattori R, Hutchison S, Ehrlich MP, Pyeritz RE, Steg PG, Greason K, Evangelista A, Kline-Rogers E, Montgomery DG, Isselbacher EM, Nienaber CA, Eagle KA.

Circulation. 2013 Sep 10;128(11 Suppl 1):S175-9. doi: 10.1161/CIRCULATIONAHA.112.000327.

PMID:
24030403
35.

RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation.

Revencu N, Boon LM, Mendola A, Cordisco MR, Dubois J, Clapuyt P, Hammer F, Amor DJ, Irvine AD, Baselga E, Dompmartin A, Syed S, Martin-Santiago A, Ades L, Collins F, Smith J, Sandaradura S, Barrio VR, Burrows PE, Blei F, Cozzolino M, Brunetti-Pierri N, Vicente A, Abramowicz M, Désir J, Vilain C, Chung WK, Wilson A, Gardiner CA, Dwight Y, Lord DJ, Fishman L, Cytrynbaum C, Chamlin S, Ghali F, Gilaberte Y, Joss S, Boente Mdel C, Léauté-Labrèze C, Delrue MA, Bayliss S, Martorell L, González-Enseñat MA, Mazereeuw-Hautier J, O'Donnell B, Bessis D, Pyeritz RE, Salhi A, Tan OT, Wargon O, Mulliken JB, Vikkula M.

Hum Mutat. 2013 Dec;34(12):1632-41. doi: 10.1002/humu.22431. Epub 2013 Oct 10.

PMID:
24038909
36.

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.

Reiff M, Mueller R, Mulchandani S, Spinner NB, Pyeritz RE, Bernhardt BA.

J Genet Couns. 2014 Aug;23(4):474-88. doi: 10.1007/s10897-013-9653-8. Epub 2013 Sep 14.

37.

Acute aortic dissection in blacks: insights from the International Registry of Acute Aortic Dissection.

Bossone E, Pyeritz RE, O'Gara P, Harris KM, Braverman AC, Pape L, Russo MJ, Hughes GC, Tsai TT, Montgomery DG, Nienaber CA, Isselbacher EM, Eagle KA; International Registry of Acute Aortic Dissection (IRAD) Investigators.

Am J Med. 2013 Oct;126(10):909-15. doi: 10.1016/j.amjmed.2013.04.020. Epub 2013 Aug 13.

PMID:
23953874
38.

Treated pulmonary arteriovenous malformations: patterns of persistence and associated retreatment success.

Woodward CS, Pyeritz RE, Chittams JL, Trerotola SO.

Radiology. 2013 Dec;269(3):919-26. doi: 10.1148/radiol.13122153. Epub 2013 Oct 28.

PMID:
23912618
39.

The IRAD classification system for characterizing survival after aortic dissection.

Booher AM, Isselbacher EM, Nienaber CA, Trimarchi S, Evangelista A, Montgomery DG, Froehlich JB, Ehrlich MP, Oh JK, Januzzi JL, O'Gara P, Sundt TM, Harris KM, Bossone E, Pyeritz RE, Eagle KA; IRAD Investigators.

Am J Med. 2013 Aug;126(8):730.e19-24. doi: 10.1016/j.amjmed.2013.01.020.

PMID:
23885677
40.

Painless Type B Aortic Dissection: Insights From the International Registry of Acute Aortic Dissection.

Tolenaar JL, Hutchison SJ, Montgomery D, O'Gara P, Fattori R, Pyeritz RE, Pape L, Suzuki T, Evangelista A, Moll FL, Rampoldi V, Isselbacher EM, Nienaber CA, Eagle KA, Trimarchi S.

Aorta (Stamford). 2013 Jul 1;1(2):96-101. doi: 10.12945/j.aorta.2013.13-014. eCollection 2013 Jul.

41.

Ethical challenges of the use of whole exome sequencing in the clinic.

Merrill SL, Vaidya A, Pyeritz RE.

World J Pediatr Congenit Heart Surg. 2013 Jan;4(1):58-61. doi: 10.1177/2150135112462590.

PMID:
23799756
42.

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians.

Bernhardt BA, Zayac C, Gordon ES, Wawak L, Pyeritz RE, Gollust SE.

Per Med. 2012 Sep 1;9(7):683-692.

43.

Angina pectoris or myocardial infarctions, pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and paradoxical emboli.

Clark K, Pyeritz RE, Trerotola SO.

Am J Cardiol. 2013 Sep 1;112(5):731-4. doi: 10.1016/j.amjcard.2013.04.052. Epub 2013 May 21.

PMID:
23707042
44.

GenTAC registry report: gender differences among individuals with genetically triggered thoracic aortic aneurysm and dissection.

Holmes KW, Maslen CL, Kindem M, Kroner BL, Song HK, Ravekes W, Dietz HC, Weinsaft JW, Roman MJ, Devereux RB, Pyeritz RE, Bavaria J, Milewski K, Milewicz D, LeMaire SA, Hendershot T, Eagle KA, Tolunay HE, Desvigne-Nickens P, Silberbach M; GenTAC Registry Consortium.

Am J Med Genet A. 2013 Apr;161A(4):779-86. doi: 10.1002/ajmg.a.35836. Epub 2013 Feb 26.

45.

Acute aortic intramural hematoma: an analysis from the International Registry of Acute Aortic Dissection.

Harris KM, Braverman AC, Eagle KA, Woznicki EM, Pyeritz RE, Myrmel T, Peterson MD, Voehringer M, Fattori R, Januzzi JL, Gilon D, Montgomery DG, Nienaber CA, Trimarchi S, Isselbacher EM, Evangelista A.

Circulation. 2012 Sep 11;126(11 Suppl 1):S91-6.

PMID:
22965999
46.

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.

Reiff M, Ross K, Mulchandani S, Propert KJ, Pyeritz RE, Spinner NB, Bernhardt BA.

Clin Genet. 2013 Jan;83(1):23-30. doi: 10.1111/cge.12004. Epub 2012 Sep 18.

47.

Aortic expansion after acute type B aortic dissection.

Jonker FH, Trimarchi S, Rampoldi V, Patel HJ, O'Gara P, Peterson MD, Fattori R, Moll FL, Voehringer M, Pyeritz RE, Hutchison S, Montgomery D, Isselbacher EM, Nienaber CA, Eagle KA; International Registry of Acute Aortic Dissection (IRAD) Investigators.

Ann Thorac Surg. 2012 Oct;94(4):1223-9. doi: 10.1016/j.athoracsur.2012.05.040. Epub 2012 Jul 7.

PMID:
22776085
48.

David L. Rimoin, MD, PhD: 1936-2012.

Pyeritz RE.

Genet Med. 2012 Jul;14(7):697-8. doi: 10.1038/gim.2012.79. No abstract available.

PMID:
22766636
49.

Clinical presentation, management, and short-term outcome of patients with type A acute dissection complicated by mesenteric malperfusion: observations from the International Registry of Acute Aortic Dissection.

Di Eusanio M, Trimarchi S, Patel HJ, Hutchison S, Suzuki T, Peterson MD, Di Bartolomeo R, Folesani G, Pyeritz RE, Braverman AC, Montgomery DG, Isselbacher EM, Nienaber CA, Eagle KA, Fattori R.

J Thorac Cardiovasc Surg. 2013 Feb;145(2):385-390.e1. doi: 10.1016/j.jtcvs.2012.01.042. Epub 2012 Feb 15.

50.

Cost savings through molecular diagnosis for hereditary hemorrhagic telangiectasia.

Bernhardt BA, Zayac C, Trerotola SO, Asch DA, Pyeritz RE.

Genet Med. 2012 Jun;14(6):604-10. doi: 10.1038/gim.2011.56. Epub 2012 Jan 26.

PMID:
22281938

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