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5 in total

1. Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

Authors: J H Ding; B Z Yang; Y Bao; C R Roe; Y T Chen
Journal: Am J Hum Genet Date: 1992-01 Impact factor: 11.025

Review 2. Prolonged QTc interval in association with medium-chain acyl-coenzyme A dehydrogenase deficiency.

Authors: Jason R Wiles; Nancy Leslie; Timothy K Knilans; Henry Akinbi
Journal: Pediatrics Date: 2014-05-05 Impact factor: 7.124

3. Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysis.

Authors: J M Penzien; G Molz; U N Wiesmann; J P Colombo; R Bühlmann; B Wermuth
Journal: Eur J Pediatr Date: 1994-05 Impact factor: 3.183

4. A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.

Authors: J C Brackett; H F Sims; R D Steiner; M Nunge; E M Zimmerman; B deMartinville; P Rinaldo; R Slaugh; A W Strauss
Journal: J Clin Invest Date: 1994-10 Impact factor: 14.808

5. Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling.

Authors: A McConkie-Rosell; A K Iafolla
Journal: J Genet Couns Date: 1993-03 Impact factor: 2.537

5 in total