131 related articles for article (PubMed ID: 34254712)
1. Subacute hypoglycemia during gastroenteritis in a child with medium-chain acyl-CoA dehydrogenase deficiency.
Nakanishi K; Okutani T; Bou R; Awano H; Yamane M
Pediatr Int; 2021 Oct; 63(10):1253-1254. PubMed ID: 34254712
[No Abstract] [Full Text] [Related]
2. Medium-chain acyl-CoA dehydrogenase deficiency: a case presentation.
Moore DJ
Neonatal Netw; 2005; 24(5):7-13. PubMed ID: 16279050
[TBL] [Abstract][Full Text] [Related]
3. Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency.
Yusuf K; Jirapradittha J; Amin HJ; Yu W; Hasan SU
Neonatology; 2010; 98(3):260-4. PubMed ID: 20414003
[TBL] [Abstract][Full Text] [Related]
4. Follow-up of fatty acid β-oxidation disorders in expanded newborn screening era.
Janeiro P; Jotta R; Ramos R; Florindo C; Ventura FV; Vilarinho L; Tavares de Almeida I; Gaspar A
Eur J Pediatr; 2019 Mar; 178(3):387-394. PubMed ID: 30617651
[TBL] [Abstract][Full Text] [Related]
5. Medium-chain acyl-Coenzyme A dehydrogenase deficiency (MCADD): a cause of severe hypoglycaemia in an apparently well child.
Maduemem KE
BMJ Case Rep; 2016 Nov; 2016():. PubMed ID: 27903579
[TBL] [Abstract][Full Text] [Related]
6. Delayed diagnosis of fatal medium-chain acyl-CoA dehydrogenase deficiency in a child.
Shetty AK; Craver RD; Harris JA; Schmidt-Sommerfeld E
Pediatr Emerg Care; 1999 Dec; 15(6):399-401. PubMed ID: 10608324
[TBL] [Abstract][Full Text] [Related]
7. Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening.
Mütze U; Nennstiel U; Odenwald B; Haase C; Ceglarek U; Janzen N; Garbade SF; Hoffmann GF; Kölker S; Haas D
Eur J Pediatr; 2022 Jun; 181(6):2415-2422. PubMed ID: 35294644
[TBL] [Abstract][Full Text] [Related]
8. Cardiac arrest in infancy: don't forget glucose!
Salter N; Quin G; Tracy E
Emerg Med J; 2010 Sep; 27(9):720-1. PubMed ID: 20798105
[TBL] [Abstract][Full Text] [Related]
9. Clinical and biochemical outcomes of patients with medium-chain acyl-CoA dehydrogenase deficiency.
Anderson DR; Viau K; Botto LD; Pasquali M; Longo N
Mol Genet Metab; 2020 Jan; 129(1):13-19. PubMed ID: 31836396
[TBL] [Abstract][Full Text] [Related]
10. Prolonged QTc interval in association with medium-chain acyl-coenzyme A dehydrogenase deficiency.
Wiles JR; Leslie N; Knilans TK; Akinbi H
Pediatrics; 2014 Jun; 133(6):e1781-6. PubMed ID: 24799540
[TBL] [Abstract][Full Text] [Related]
11. Medium-chain Acyl-COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment.
Mason E; Hindmarch CCT; Dunham-Snary KJ
Endocrinol Diabetes Metab; 2023 Jan; 6(1):e385. PubMed ID: 36300606
[TBL] [Abstract][Full Text] [Related]
12. A nationwide retrospective observational study of population newborn screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in the Netherlands.
Jager EA; Kuijpers MM; Bosch AM; Mulder MF; Gozalbo ER; Visser G; de Vries M; Williams M; Waterham HR; van Spronsen FJ; Schielen PCJI; Derks TGJ
J Inherit Metab Dis; 2019 Sep; 42(5):890-897. PubMed ID: 31012112
[TBL] [Abstract][Full Text] [Related]
13. VERY LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY: CASE REPORT OF HYPOGLYCAEMIA AND RHABDOMYOLYSIS IN A 2-DAY-OLD INFANT.
Kiss S; Hong KM; Sadowsky J; Greaves RF; Yaplito-Lee J
J Paediatr Child Health; 2020 Dec; 56(12):1996-1997. PubMed ID: 33351248
[No Abstract] [Full Text] [Related]
14. 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
Mol Genet Metab; 2020 Jan; 129(1):20-25. PubMed ID: 31813752
[TBL] [Abstract][Full Text] [Related]
15. Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency.
McGregor TL; Berry SA; Dipple KM; Hamid R;
Pediatrics; 2021 Jan; 147(1):. PubMed ID: 33372121
[TBL] [Abstract][Full Text] [Related]
16. Diagnostic potential of stored dried blood spots for inborn errors of metabolism: a metabolic autopsy of medium-chain acyl-CoA dehydrogenase deficiency.
Kaku N; Ihara K; Hirata Y; Yamada K; Lee S; Kanemasa H; Motomura Y; Baba H; Tanaka T; Sakai Y; Maehara Y; Ohga S
J Clin Pathol; 2018 Oct; 71(10):885-889. PubMed ID: 29720407
[TBL] [Abstract][Full Text] [Related]
17. Sweet and sour aspects of medium-chain acyl CoA dehydrogenase deficiency. Commentary on K. Yusuf et al.: Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency (Neonatology 2010;98:260-264).
Derks TG
Neonatology; 2010; 98(3):265-7. PubMed ID: 20414004
[No Abstract] [Full Text] [Related]
18. [Infant coma in the emergency department: 2 cases of MCAD deficiency].
Hoflack M; Caruba C; Pitelet G; Haas H; Mas JC; Paquis V; Berard E
Arch Pediatr; 2010 Jul; 17(7):1074-7. PubMed ID: 20434892
[TBL] [Abstract][Full Text] [Related]
19. Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency.
Derks TG; Boer TS; van Assen A; Bos T; Ruiter J; Waterham HR; Niezen-Koning KE; Wanders RJ; Rondeel JM; Loeber JG; Ten Kate LP; Smit GP; Reijngoud DJ
J Inherit Metab Dis; 2008 Feb; 31(1):88-96. PubMed ID: 18188679
[TBL] [Abstract][Full Text] [Related]
20. A novel tandem mass spectrometry method for rapid confirmation of medium- and very long-chain acyl-CoA dehydrogenase deficiency in newborns.
ter Veld F; Mueller M; Kramer S; Haussmann U; Herebian D; Mayatepek E; Laryea MD; Primassin S; Spiekerkoetter U
PLoS One; 2009 Jul; 4(7):e6449. PubMed ID: 19649258
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]