Smoot LB - Search Results

1

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.

Warejko JK, Schueler M, Vivante A, Tan W, Daga A, Lawson JA, Braun DA, Shril S, Amann K, Somers MJG, Rodig NM, Baum MA, Daouk G, Traum AZ, Kim HB, Vakili K, Porras D, Lock J, Rivkin MJ, Chaudry G, Smoot LB, Singh MN, Smith ER, Mane SM, Lifton RP, Stein DR, Ferguson MA, Hildebrandt F. Warejko JK, et al. Among authors: smoot lb. Hypertension. 2018 Apr;71(4):691-699. doi: 10.1161/HYPERTENSIONAHA.117.10296. Epub 2018 Feb 26. Hypertension. 2018. PMID: 29483232 Free PMC article.

2

Mechanisms of premature vascular aging in children with Hutchinson-Gilford progeria syndrome.

Gerhard-Herman M, Smoot LB, Wake N, Kieran MW, Kleinman ME, Miller DT, Schwartzman A, Giobbie-Hurder A, Neuberg D, Gordon LB. Gerhard-Herman M, et al. Among authors: smoot lb. Hypertension. 2012 Jan;59(1):92-7. doi: 10.1161/HYPERTENSIONAHA.111.180919. Epub 2011 Nov 14. Hypertension. 2012. PMID: 22083160 Free PMC article. Clinical Trial.

3

Outcomes after primary transcatheter therapy in infants and young children with severe bilateral peripheral pulmonary artery stenosis.

Cunningham JW, McElhinney DB, Gauvreau K, Bergersen L, Lacro RV, Marshall AC, Smoot L, Lock JE. Cunningham JW, et al. Circ Cardiovasc Interv. 2013 Aug;6(4):460-7. doi: 10.1161/CIRCINTERVENTIONS.112.000061. Epub 2013 Aug 13. Circ Cardiovasc Interv. 2013. PMID: 23941859

4

Surgical management of pediatric renovascular hypertension and midaortic syndrome at a single-center multidisciplinary program.

Kim SS, Stein DR, Ferguson MA, Porras D, Chaudry G, Singh MN, Smoot L, Kim HB, Vakili K. Kim SS, et al. J Vasc Surg. 2021 Jul;74(1):79-89.e2. doi: 10.1016/j.jvs.2020.12.053. Epub 2020 Dec 16. J Vasc Surg. 2021. PMID: 33340698 Free article.

5

Elastin gene deletions in Williams syndrome.

Smoot LB. Smoot LB. Curr Opin Pediatr. 1995 Dec;7(6):698-701. doi: 10.1097/00008480-199512000-00013. Curr Opin Pediatr. 1995. PMID: 8776022 Review.

6

Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases.

Wu CW, Caha M, Smoot L, Harris DJ, Roberts AE, Sacharow S, Bodamer O. Wu CW, et al. Mol Genet Metab. 2023 Jul;139(3):107626. doi: 10.1016/j.ymgme.2023.107626. Epub 2023 Jun 10. Mol Genet Metab. 2023. PMID: 37354892 Review.

7

Familial dilated cardiomyopathy secondary to dystrophin splice site mutation.

Obler D, Wu BL, Lip V, Estrella E, Keck S, Haggan C, Semigran M, Smoot LB. Obler D, et al. Among authors: smoot lb. J Card Fail. 2010 Mar;16(3):194-9. doi: 10.1016/j.cardfail.2009.11.009. J Card Fail. 2010. PMID: 20206892

8

Integrin β3 inhibition is a therapeutic strategy for supravalvular aortic stenosis.

Misra A, Sheikh AQ, Kumar A, Luo J, Zhang J, Hinton RB, Smoot L, Kaplan P, Urban Z, Qyang Y, Tellides G, Greif DM. Misra A, et al. J Exp Med. 2016 Mar 7;213(3):451-63. doi: 10.1084/jem.20150688. Epub 2016 Feb 8. J Exp Med. 2016. PMID: 26858344 Free PMC article.

9

Extracorporeal Membrane Oxygenation Support After Heart Transplantation in Children-Outcomes of a Single Center Cohort.

Nair AG, Sleeper LA, Smoot LB, Wigmore D, Mecklosky J, Andren K, Bastardi HJ, Blume ED, Fynn-Thompson F, Thiagarajan RR, Alexander PMA. Nair AG, et al. Among authors: smoot lb. Pediatr Crit Care Med. 2020 Apr;21(4):332-339. doi: 10.1097/PCC.0000000000002192. Pediatr Crit Care Med. 2020. PMID: 31658187

10

Elastin: mutational spectrum in supravalvular aortic stenosis.

Metcalfe K, Rucka AK, Smoot L, Hofstadler G, Tuzler G, McKeown P, Siu V, Rauch A, Dean J, Dennis N, Ellis I, Reardon W, Cytrynbaum C, Osborne L, Yates JR, Read AP, Donnai D, Tassabehji M. Metcalfe K, et al. Eur J Hum Genet. 2000 Dec;8(12):955-63. doi: 10.1038/sj.ejhg.5200564. Eur J Hum Genet. 2000. PMID: 11175284

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