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1,991 Possible Causes for AA, ERR, INBORN, METAB

  • Caffeine

    During the 24 h following the test, AA homozygotes tended to experience increased insomnia with caffeine while C-allele carriers did not present this effect.[ncbi.nlm.nih.gov] Diabetes Metab Syndr. 2017 Dec;11 Suppl 2:S631-S635. doi: 10.1016/j.dsx.2017.04.017. Epub 2017 Apr 23.[ncbi.nlm.nih.gov] We evaluated inborn, VLBW infants discharged from 2000 to 2014, who received only CPAP therapy without surfactant treatment on day of life (DOL) 0, had a 5-minute Apgar 3,[ncbi.nlm.nih.gov] To err on the side of caution, the American College of Obstetricians and Gynecologists (ACOG) advises pregnant women to limit their caffeine intake to less than 200 milligrams[babycenter.com]

  • Motor Neuron Disease

    Ratings from ‘AA’ to ‘CCC’ may be modified by the addition of a plus ( ) or minus (-) sign to show relative standing within the major rating categories.[southerncross.co.nz] Mol Genet Metab. 2013 Jan;108(1):65-9. doi: 10.1016/j.ymgme.2012.10.023. Epub 2012 Nov 2.[ncbi.nlm.nih.gov] KEYWORDS: Amyotrophic lateral sclerosis; Inborn errors of metabolism; Motor neuron disease; Neurogenetics; Neurometabolic disorders[ncbi.nlm.nih.gov] The rating scale is: AAA (Extremely Strong), AA (Very Strong), A (Strong), BBB (Good), BB (Marginal), B (Weak), CCC (Very Weak), CC (Extremely Weak), SD or D (Selective Default[southerncross.co.nz]

    Missing: ERR
  • Keratitis

    Tuli SS, Kubal AA. Herpes simplex keratitis. In: Yanoff M, Duker JS, eds. Ophthalmology . 4th ed. Philadelphia, PA: Elsevier Saunders; 2014:chap 4.15.[medlineplus.gov] J Inherit Metab Dis. 2017 May;40(3):461-462. doi: 10.1007/s10545-016-9996-z. Epub 2016 Nov 10.[ncbi.nlm.nih.gov] Always err on the side of being too cautious and never be afraid of referring any infectious ulcer that appears to be progressive and unresponsive to treatment.[healio.com] Abstract Richner-Hanhart syndrome (RHS, tyrosinemia type II) is a rare, autosomal recessive inborn error of tyrosine metabolism caused by tyrosine aminotransferase deficiency[ncbi.nlm.nih.gov]

  • Phenobarbital

    Propane Propylene Roflurane Sevoflurane Synthane Teflurane Toluene Trichloroethane (methyl chloroform) Trichloroethylene Vinyl ether Others/unsorted 3-Hydroxybutanal α-EMTBL AA[en.wikipedia.org] Drug Metab Dispos. 2017 May;45(5):532-539. doi: 10.1124/dmd.116.074872. Epub 2017 Mar 29.[ncbi.nlm.nih.gov] Most sources recommend a moderately increased dose guided by therapeutic drug monitoring.A 14 year old boy with nonketotic hyperglycinemia, a rare inborn error of metabolism[ncbi.nlm.nih.gov] For critically ill patients, the intravenous route is typically used to err on the side of safety.[emcrit.org]

  • Bacillus Subtilis

    32,626 November 1, 1990 - v2 A28AEFFDB1316684 GO Experimental Info Feature key Position(s) Description Actions Graphical view Length Sequence conflict i 101 – 102 GT TG AA[uniprot.org] Abstract Bacillus subtilis is generally accepted as an inborn host candidate employed for secretory production of heterologous proteins.[ncbi.nlm.nih.gov]

    Missing: ERR
  • Endocrine Dysfunction

    Wilson M, Morganti AA, Zervoudakis I, et al. Blood pressure, the renin-aldosterone system and sex steroids throughout normal pregnancy. Am J Med . 1980;68(1):97-104.[now.aapmr.org] Metab. Dis. 27 , 349–362 (2004). 3. Pagano, G. et al .[nature.com] Recent research into the role alternative hormonal axes play in spermatogenesis and promising new technologies that may correct inborn or acquired endocrinopathies leading[ncbi.nlm.nih.gov] Horm Metab Res 2006;38:587-91. 15. Åberg ND, Brywe KG, Isgaard J.[annalsofian.org]

    Missing: ERR
  • Phenylketonuria

    Twelve received CGMP-AA and nine received Phe-free L-AA, (1 CGMP-AA withdrawal). Subjects partially or wholly replaced Phe-free L-AA with CGMP-AA.[ncbi.nlm.nih.gov] Metab. 91 , 48–54 (2007). 28. Lou, H.[nature.com] Abstract Phenylketonuria is an autosomal recessive inborn error of metabolism which can be prevented by early and continuous treatment.[ncbi.nlm.nih.gov] […] hyperphenylalaninaemia (HPA) kezelésére javasolt phenylketonuriában (PKU) szenvedő felnőttek és # éves vagy annál idősebb gyermekek számára, akik bizonyítottan reagálnak erre[hu.glosbe.com]

  • Maple Syrup Urine Disease

    (PDGF-AA)[ncbi.nlm.nih.gov] ., (2003) Mol Genet Metab 80:189-195 Flaschker et al., (2007) J Inherit Metab Dis 30:903-909 Quental et al., (2008) Mol Genet Metab 94:148-156 Forms and Documents Test Details[genedx.com] Abstract The New South Wales state-wide newborn screening programme has offered comprehensive screening for inborn errors of metabolism, including MSUD, using electrospray[ncbi.nlm.nih.gov] KEYWORDS: Inborn amino acidopathies; Inborn errors of metabolism; Inherited metabolic disorders; Maple syrup urine disease; Nutrition therapy/diet therapy; Practice guidelines[ncbi.nlm.nih.gov]

    Missing: ERR
  • Zileuton

    Pretreatment with zileuton partially prevented the AA-induced LTB(4) and IL-6 release and increased neutral lipid content.[ncbi.nlm.nih.gov] .: Metab. Dispos., 20, 328 (1992), All Products are stable to be shipped at room temperature, unless otherwise specified.[trc-canada.com] The Sjögren-Larsson syndrome (SLS) is an inborn error of lipid metabolism, characterised clinically by congenital ichthyosis, mental retardation and spasticity.[ncbi.nlm.nih.gov] Drug Metab Dispos. 1995 Oct;23(10):1163-74. [ PubMed:8654206 ] Zileuton FDA [ File ] Property Measurement pH Temperature ( C) References Ki (nM) 117000 N/A N/A 16248836 Ki[drugbank.ca]

    Missing: ERR
  • Enalapril

    A multiple linear regression analysis showed that the AA genotype for the g.-2578C A polymorphism and the AGG haplotype are associated with more intense decrease in blood[ncbi.nlm.nih.gov] Ulm, Drug Metab. Rev. 1983 , 14 , 99. Enalapril.[tcichemicals.com] […] adverse events, including postnatal age at first exposure, exposure duration, gestational age group, small for gestational age status, race, sex, 5-min Apgar score, and inborn[ncbi.nlm.nih.gov] Drug Metab. Dispos. 10: 15-19. PMID: 6124377 2. Sweet, C.S. 1983. Fed. Proc. 42: 167-170. PMID: 6295819 3. Cleary, J.D. and Taylor, J.W. 1986.[scbt.com]

    Missing: ERR