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Page 1
Congenital Hypothyroidism 3-Year Follow-Up Project: Region 4 Midwest Genetics Collaborative Results.
Int J Neonatal Screen. 2018 Jun 17;4(2):18. doi: 10.3390/ijns4020018. eCollection 2018 Jun.
Int J Neonatal Screen. 2018.
PMID: 33072941
Free PMC article.
Utility of specific amino acid ratios in screening for pyruvate dehydrogenase complex deficiencies and other mitochondrial disorders associated with congenital lactic acidosis and newborn screening prospects.
Bedoyan JK, Hage R, Shin HK, Linard S, Ferren E, Ducich N, Wilson K, Lehman A, Schillaci LA, Manickam K, Mori M, Bartholomew D, DeBrosse S, Cohen B, Parikh S, Kerr D.
Bedoyan JK, et al. Among authors: linard s.
JIMD Rep. 2020 Aug 16;56(1):70-81. doi: 10.1002/jmd2.12153. eCollection 2020 Nov.
JIMD Rep. 2020.
PMID: 33204598
Free PMC article.
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Congenital Hypothyroidism Long-Term Follow-up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Project.
Wintergerst K, Gembel G, Kreipe T, Zeller P, Eugster E, Young B, Andruszewski K, Kleyn M, Cunningham T, Fawbush S, Vanderburg N, Sockalosky J, Menon R, Linard S, Hoffman G, Gorman L.
Wintergerst K, et al. Among authors: linard s.
J Genet Couns. 2015 Jun;24(3):464-72. doi: 10.1007/s10897-014-9790-8. Epub 2014 Nov 18.
J Genet Couns. 2015.
PMID: 25403899
Free PMC article.
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The effects of gestational age and birth weight on false-positive newborn-screening rates.
Slaughter JL, Meinzen-Derr J, Rose SR, Leslie ND, Chandrasekar R, Linard SM, Akinbi HT.
Slaughter JL, et al. Among authors: linard sm.
Pediatrics. 2010 Nov;126(5):910-6. doi: 10.1542/peds.2010-0943. Epub 2010 Oct 25.
Pediatrics. 2010.
PMID: 20974783
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Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.
McHugh D, Cameron CA, Abdenur JE, Abdulrahman M, Adair O, Al Nuaimi SA, Åhlman H, Allen JJ, Antonozzi I, Archer S, Au S, Auray-Blais C, Baker M, Bamforth F, Beckmann K, Pino GB, Berberich SL, Binard R, Boemer F, Bonham J, Breen NN, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Cariappa R, Carlisle C, Caruso U, Cassanello M, Castilla AM, Ramos DE, Chakraborty P, Chandrasekar R, Ramos AC, Cheillan D, Chien YH, Childs TA, Chrastina P, Sica YC, de Juan JA, Colandre ME, Espinoza VC, Corso G, Currier R, Cyr D, Czuczy N, D'Apolito O, Davis T, de Sain-Van der Velden MG, Delgado Pecellin C, Di Gangi IM, Di Stefano CM, Dotsikas Y, Downing M, Downs SM, Dy B, Dymerski M, Rueda I, Elvers B, Eaton R, Eckerd BM, El Mougy F, Eroh S, Espada M, Evans C, Fawbush S, Fijolek KF, Fisher L, Franzson L, Frazier DM, Garcia LR, Bermejo MS, Gavrilov D, Gerace R, Giordano G, Irazabal YG, Greed LC, Grier R, Grycki E, Gu X, Gulamali-Majid F, Hagar AF, Han L, Hannon WH, Haslip C, Hassan FA, He M, Hietala A, Himstedt L, Hoffman GL, Hoffman W, Hoggatt P, Hopkins PV, Hougaard DM, Hughes K, Hunt PR, Hwu WL, Hynes J, Ibarra…
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McHugh D, et al. Among authors: linard s.
Genet Med. 2011 Mar;13(3):230-54. doi: 10.1097/GIM.0b013e31820d5e67.
Genet Med. 2011.
PMID: 21325949
Free article.
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Finding blunders in thyroid testing: experience in newborns.
Zilka LJ, Lott JA, Baker LC, Linard SM.
Zilka LJ, et al. Among authors: linard sm.
J Clin Lab Anal. 2008;22(4):254-6. doi: 10.1002/jcla.20247.
J Clin Lab Anal. 2008.
PMID: 18623119
Free PMC article.
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Sequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency.
McCandless SE, Chandrasekar R, Linard S, Kikano S, Rice L.
McCandless SE, et al. Among authors: linard s.
Mol Genet Metab. 2013 Jan;108(1):51-5. doi: 10.1016/j.ymgme.2012.10.016. Epub 2012 Oct 24.
Mol Genet Metab. 2013.
PMID: 23151387
Free PMC article.
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