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Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders.
Mol Genet Metab. 2021 Jan;132(1):19-26. doi: 10.1016/j.ymgme.2020.12.002. Epub 2020 Dec 23.
Mol Genet Metab. 2021.
PMID: 33388234
Free PMC article.
Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency.
Diaz GA, Schulze A, McNutt MC, Leão-Teles E, Merritt JL 2nd, Enns GM, Batzios S, Bannick A, Zori RT, Sloan LS, Potts SL, Bubb G, Quinn AG.
Diaz GA, et al.
J Inherit Metab Dis. 2021 Jul;44(4):847-856. doi: 10.1002/jimd.12343. Epub 2021 Jan 26.
J Inherit Metab Dis. 2021.
PMID: 33325055
Free PMC article.
Clinical Trial.
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Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblings.
Bannick A, Chase S, Miner A, Seeterlin M, Conway RL.
Bannick A, et al.
Eur J Med Genet. 2020 Dec;63(12):104076. doi: 10.1016/j.ejmg.2020.104076. Epub 2020 Sep 24.
Eur J Med Genet. 2020.
PMID: 32980525
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Mild Persistent Isolated Hypermethioninemia Identified through Newborn Screening in Michigan.
Sen K, Felice MD, Bannick A, Colombo R, Conway RL.
Sen K, et al.
J Pediatr Genet. 2019 Jun;8(2):54-57. doi: 10.1055/s-0039-1683900. Epub 2019 Mar 27.
J Pediatr Genet. 2019.
PMID: 31061746
Free PMC article.
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Outcomes of referrals to Child Protective Services for medical neglect in patients with phenylketonuria: Experiences at a single treatment center.
Bannick AA, Laufman JD, Edwards HL, Ventimiglia J, Feldman GL.
Bannick AA, et al.
Mol Genet Metab. 2015 Aug;115(4):151-6. doi: 10.1016/j.ymgme.2015.06.003. Epub 2015 Jun 16.
Mol Genet Metab. 2015.
PMID: 26138304
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Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.
Chien YH, Abdenur JE, Baronio F, Bannick AA, Corrales F, Couce M, Donner MG, Ficicioglu C, Freehauf C, Frithiof D, Gotway G, Hirabayashi K, Hofstede F, Hoganson G, Hwu WL, James P, Kim S, Korman SH, Lachmann R, Levy H, Lindner M, Lykopoulou L, Mayatepek E, Muntau A, Okano Y, Raymond K, Rubio-Gozalbo E, Scholl-Bürgi S, Schulze A, Singh R, Stabler S, Stuy M, Thomas J, Wagner C, Wilson WG, Wortmann S, Yamamoto S, Pao M, Blom HJ.
Chien YH, et al. Among authors: bannick aa.
Orphanet J Rare Dis. 2015 Aug 20;10:99. doi: 10.1186/s13023-015-0321-y.
Orphanet J Rare Dis. 2015.
PMID: 26289392
Free PMC article.
Review.
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The inborn errors of metabolism information system: A project of the Region 4 Genetics Collaborative Priority 2 Workgroup.
Berry SA, Jurek AM, Anderson C, Bentler K; Region 4 Genetics Collaborative Priority 2 Workgroup.
Berry SA, et al.
Genet Med. 2010 Dec;12(12 Suppl):S215-9. doi: 10.1097/GIM.0b013e3181fe5d23.
Genet Med. 2010.
PMID: 21150367
Free article.
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Parental strategies to help children with phenylketonuria (PKU) cope with feeling different.
Zwiesele S, Bannick A, Trepanier A.
Zwiesele S, et al.
Am J Med Genet A. 2015 Aug;167A(8):1787-95. doi: 10.1002/ajmg.a.37088. Epub 2015 Apr 29.
Am J Med Genet A. 2015.
PMID: 25920535
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