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Year | Number of Results |
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2004 | 1 |
2011 | 1 |
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Page 1
Georgia state spinal muscular atrophy newborn screening experience: Screening assay performance and early clinical outcomes.
Am J Med Genet C Semin Med Genet. 2022 Jun;190(2):187-196. doi: 10.1002/ajmg.c.32003. Epub 2022 Sep 26.
Am J Med Genet C Semin Med Genet. 2022.
PMID: 36164257
Newborn Screening for X-Linked Adrenoleukodystrophy in Georgia: Experiences from a Pilot Study Screening of 51,081 Newborns.
Hall PL, Li H, Hagar AF, Jerris SC, Wittenauer A, Wilcox W.
Hall PL, et al. Among authors: hagar af.
Int J Neonatal Screen. 2020 Oct 23;6(4):81. doi: 10.3390/ijns6040081.
Int J Neonatal Screen. 2020.
PMID: 33239602
Free PMC article.
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Two-Tiered Newborn Screening with Post-Analytical Tools for Pompe Disease and Mucopolysaccharidosis Type I Results in Performance Improvement and Future Direction.
Hall PL, Sanchez R, Hagar AF, Jerris SC, Wittenauer A, Wilcox WR.
Hall PL, et al. Among authors: hagar af.
Int J Neonatal Screen. 2020 Mar;6(1):2. doi: 10.3390/ijns6010002. Epub 2020 Jan 14.
Int J Neonatal Screen. 2020.
PMID: 32064362
Free PMC article.
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Increased parental anxiety and a benign clinical course: Infants identified with short-chain acyl-CoA dehydrogenase deficiency and isobutyryl-CoA dehydrogenase deficiency through newborn screening in Georgia.
Sadat R, Hall PL, Wittenauer AL, Vengoechea ED, Park K, Hagar AF, Singh R, Moore RH, Gambello MJ.
Sadat R, et al. Among authors: hagar af.
Mol Genet Metab. 2020 Jan;129(1):20-25. doi: 10.1016/j.ymgme.2019.11.008. Epub 2019 Nov 27.
Mol Genet Metab. 2020.
PMID: 31813752
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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,…
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McHugh D, et al. Among authors: hagar af.
Genet Med. 2011 Mar;13(3):230-54. doi: 10.1097/GIM.0b013e31820d5e67.
Genet Med. 2011.
PMID: 21325949
Free article.
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Diagnosis and characterization of Hb C/Hb Iowa: a rare but easily misidentified compound heterozygous condition.
Somjee S, Yu LC, Hagar AF, Hempe JM.
Somjee S, et al. Among authors: hagar af.
Hemoglobin. 2004 Feb;28(1):7-13. doi: 10.1081/hem-120028882.
Hemoglobin. 2004.
PMID: 15008260
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