|1.||Wanders, Ronald J A: 4 articles (01/2015 - 07/2004)|
|2.||Shigematsu, Yosuke: 3 articles (01/2015 - 01/2004)|
|3.||Gu, Xue-Fan: 3 articles (05/2014 - 02/2008)|
|4.||Ye, Jun: 3 articles (05/2014 - 12/2007)|
|5.||Han, Lian-Shu: 3 articles (05/2014 - 02/2008)|
|6.||Strauss, Arnold W: 3 articles (02/2014 - 08/2002)|
|7.||Matern, Dietrich: 3 articles (03/2009 - 08/2006)|
|8.||Strauss, A W: 3 articles (11/2001 - 06/2001)|
|9.||Waterham, Hans R: 2 articles (01/2015 - 10/2007)|
|10.||Tajima, Go: 2 articles (01/2015 - 12/2013)|
|1.||Sudden Infant Death (SID)
01/01/2015 - "A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis."
08/01/2010 - "We report a 21-year-old primigravida with a previously characterized VLCAD deficiency, who experienced frequent and unprovoked episodes of rhabdomyolysis before pregnancy. "
05/01/2003 - "We emphasize that muscular form of VLCAD deficiency should be regarded as one of the causes of recurrent rhabdomyolysis in adult."
05/01/2003 - "Several reports showed that muscular form (adult onset form) of VLCAD deficiency demonstrated recurrent rhabdomyolysis, but true 'adult-onset' case with VLCAD deficiency have been rarely reported. "
05/01/2003 - "[Very-long-chain acyl-CoA dehydrogenase deficiency presenting with recurrent rhabdomyolysis in an adult]."
09/01/2013 - "Successful Treatment of Cardiomyopathy due to Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: First Case Report from Oman with Literature Review."
06/01/2008 - "VLCAD deficiency is a fatty acid oxidation disease leading to cardiomyopathy and arrhythmias. "
12/01/1998 - "late-onset VLCAD deficiency may present as acute cardiomyopathy."
08/01/1998 - "Clinical recognition of VLCAD deficiency is important because it is one of the few directly treatable causes of cardiomyopathy in children."
06/01/1996 - "Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy."
|4.||Hypoglycemia (Reactive Hypoglycemia)
03/01/2009 - "We report a 20-year-old female with VLCAD deficiency who first presented in infancy with hypoketotic hypoglycemia. "
02/01/2014 - "Patients with VLCAD deficiency present with hypoketotic hypoglycemia and cardiomyopathy, which can be exacerbated by fasting and/or cold stress. "
03/01/2006 - "We report on a mouse model of VLCAD deficiency with a phenotype induced by the stresses of fasting and cold, which includes hypoglycemia, hypothermia, and severe bradycardia. "
07/01/2001 - "The phenotype of VLCAD deficiency is heterogeneous, ranging from catastrophic metabolic and cardiac failure in infancy to mild hypoketotic, hypoglycemia, and exertional rhabdomyolysis in adults. "
03/01/2006 - "Mitochondrial very-long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is associated with severe hypoglycemia, cardiac dysfunction, and sudden death in neonates and children. "
|5.||Muscular Diseases (Myopathy)
07/01/1999 - "Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype."
12/01/2007 - "Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency is an inborn mitochondrial fatty-acid beta-oxidation (FAO) defect associated with a broad mutational spectrum, with phenotypes ranging from fatal cardiopathy in infancy to adolescent-onset myopathy, and for which there is no established treatment. "
05/01/2010 - "Very-Long-Chain Acyl-CoA Dehydrogenase deficiency (VLCADD) is an autosomal recessive disorder considered as one of the more common ss-oxidation defects, possibly associated with neonatal cardiomyopathy, infantile hepatic coma, or adult-onset myopathy. "
03/01/2009 - "Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency is a disorder of oxidation of long chain fat, and can present as cardiomyopathy or fasting intolerance in the first months to years of life, or as myopathy in later childhood to adulthood. "
06/22/2004 - "Muscle pathology is often unhelpful in elucidating the specific underlying abnormality in patients with metabolic myopathy with rhabdomyolysis, including very-long chain acyl-CoA dehydrogenase (VLCAD) deficiency. "
|1.||Carnitine O-Palmitoyltransferase (Carnitine Palmitoyltransferase II)
|2.||Long-Chain Acyl-CoA Dehydrogenase (Long-Chain-Acyl-Coenzyme A Dehydrogenase)
|3.||Medium chain acyl CoA dehydrogenase deficiency
|4.||Coenzyme A (CoA)
|5.||Short chain Acyl CoA dehydrogenase deficiency
|9.||Acyl-CoA Dehydrogenase (Medium-Chain Acyl-Coenzyme A Dehydrogenase)
|1.||Intensive Care (Surgical Intensive Care)