320 related articles for article (PubMed ID: 2718899)
1. Medium-chain acyl-CoA dehydrogenase deficiency.
Egidio RJ; Francis GL; Coates PM; Hale DE; Roesel A
Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899
[TBL] [Abstract][Full Text] [Related]
2. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency].
Collet JP; Divry P; Blanc JF; Guibaud P; David M; Macabeo V; Vibert J; Hermier M
Pediatrie; 1984 Dec; 39(8):661-8. PubMed ID: 6535973
[TBL] [Abstract][Full Text] [Related]
3. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome].
Brus F; Smit GP; Knoester H; Reijngoud DJ
Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055
[TBL] [Abstract][Full Text] [Related]
4. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
Rinaldo P; O'Shea JJ; Coates PM; Hale DE; Stanley CA; Tanaka K
N Engl J Med; 1988 Nov; 319(20):1308-13. PubMed ID: 3054550
[TBL] [Abstract][Full Text] [Related]
5. [Medium-chain acyl-CoA dehydrogenase defect. Acute cerebral episodes and nonketotic hypoglycemia in children].
von Mühlendahl KE; Lehnert W; Mönch E
Dtsch Med Wochenschr; 1990 Aug; 115(33):1235-8. PubMed ID: 2387217
[TBL] [Abstract][Full Text] [Related]
6. Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency.
Taubman B; Hale DE; Kelley RI
Pediatrics; 1987 Mar; 79(3):382-5. PubMed ID: 3822638
[TBL] [Abstract][Full Text] [Related]
7. MCAD deficiency: what family physicians need to know.
Siwek J
Am Fam Physician; 1989 May; 39(5):116, 119. PubMed ID: 2718890
[No Abstract] [Full Text] [Related]
8. Frequency of medium-chain acyl-CoA dehydrogenase deficiency G-985 mutation in sudden infant death syndrome.
Miller ME; Brooks JG; Forbes N; Insel R
Pediatr Res; 1992 Apr; 31(4 Pt 1):305-7. PubMed ID: 1570195
[TBL] [Abstract][Full Text] [Related]
9. Inborn defects of fatty acid oxidation: a preventable cause of SIDS.
Keppen LD; Randall B
S D J Med; 1999 Jun; 52(6):187-8; disscussion 188-9. PubMed ID: 10388343
[TBL] [Abstract][Full Text] [Related]
10. Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies.
Ziadeh R; Hoffman EP; Finegold DN; Hoop RC; Brackett JC; Strauss AW; Naylor EW
Pediatr Res; 1995 May; 37(5):675-8. PubMed ID: 7603790
[TBL] [Abstract][Full Text] [Related]
11. [Medium-chain acyl-CoA dehydrogenase deficiency].
Uchiyama A; Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):68-70. PubMed ID: 11596453
[No Abstract] [Full Text] [Related]
12. Diagnosis of mitochondrial fatty acid oxidation defects.
Duran M; Bruinvis L; Ketting D; Dorland L
Padiatr Padol; 1993; 28(1):19-25. PubMed ID: 8446424
[TBL] [Abstract][Full Text] [Related]
13. The Brugada ECG pattern in a neonate.
Sanatani S; Mahkseed N; Vallance H; Brugada R
J Cardiovasc Electrophysiol; 2005 Mar; 16(3):342-4. PubMed ID: 15817096
[TBL] [Abstract][Full Text] [Related]
14. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population.
Kozàk L; Hrabincovà E; Rudolfoà J; Vràbelovà S; Freiberger T
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():49-50. PubMed ID: 11400780
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.
Brackett JC; Sims HF; Steiner RD; Nunge M; Zimmerman EM; deMartinville B; Rinaldo P; Slaugh R; Strauss AW
J Clin Invest; 1994 Oct; 94(4):1477-83. PubMed ID: 7929823
[TBL] [Abstract][Full Text] [Related]
16. [Screening of A985 to G mutation of medium-chain acyl-CoA dehydrogenase (MCAD) gene in Normandy. Evaluation of the role of MCAD deficiency in sudden infant death].
Lecoq I; Mallet E; Bonté JB; Laroche D; Travert G
C R Seances Soc Biol Fil; 1995; 189(2):295-301. PubMed ID: 8590228
[TBL] [Abstract][Full Text] [Related]
17. Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndrome.
Santer R; Schmidt-Sommerfeld E; Leung YK; Fischer JE; Lebenthal E
Eur J Pediatr; 1990 Dec; 150(2):111-4. PubMed ID: 2279505
[TBL] [Abstract][Full Text] [Related]
18. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels.
Stanley CA; Hale DE; Coates PM; Hall CL; Corkey BE; Yang W; Kelley RI; Gonzales EL; Williamson JR; Baker L
Pediatr Res; 1983 Nov; 17(11):877-84. PubMed ID: 6646897
[TBL] [Abstract][Full Text] [Related]
19. Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency.
Andresen BS; Bross P; Jensen TG; Knudsen I; Winter V; Kølvraa S; Bolund L; Gregersen N
Scand J Clin Lab Invest Suppl; 1995; 220():9-25. PubMed ID: 7652482
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.
Kelly DP; Whelan AJ; Hale DE; Rinaldo P; Rutledge SL; Zhang Z; Strauss AW
Prog Clin Biol Res; 1992; 375():463-72. PubMed ID: 1438388
[No Abstract] [Full Text] [Related]
[Next] [New Search]