Placental Floor Infarction Complicating the Pregnancy of a Fetus with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency

By Matern D.   Schehata B.M.   Shekhawa P.   Strauss A.W.   Bennett M.J.   Rinaldo P.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 3, 2001-03 ,pp. : 265-268

Academic Press

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Early Neonatal Diagnosis of Long-Chain 3-Hydroxyacyl Coenzyme A Dehydrogenase and Mitochondrial Trifunctional Protein Deficiencies

By Hintz S.R.   Matern D.   Strauss A.   Bennett M.J.   Hoyme H.E.   Schelley S.   Kobori J.   Colby C.   Lehman N.L.   Enns G.M.  

Molecular Genetics and Metabolism, Vol. 75, Iss. 2, 2002-02 ,pp. : 120-127

Elsevier

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Identification and Characterization of Temperature-Sensitive Mild Mutations in Three Japanese Patients with Nonsevere Forms of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency

By Takusa Y.   Fukao T.   Kimura M.   Uchiyama A.   Abo W.   Tsuboi Y.   Hirose S.   Fujioka H.   Kondo N.   Yamaguchi S.  

Molecular Genetics and Metabolism, Vol. 75, Iss. 3, 2002-03 ,pp. : 227-234

Academic Press

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Identification of a Novel Mutation in Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency

By Yang B-Z.   Ding J-H.   Zhou C.   Dimachkie M.M.   Sweetman L.   Dasouki M.J.   Wilkinson J.   Roe C.R.  

Molecular Genetics and Metabolism, Vol. 69, Iss. 3, 2000-03 ,pp. : 259-262

Academic Press

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A Polymorphic Variant in the Human Electron Transfer Flavoprotein α-Chain (α-T171) Displays Decreased Thermal Stability and Is Overrepresented in Very-Long-Chain acyl-CoA Dehydrogenase-Deficient Patients with Mild Childhood Presentation

By Bross P.   Pedersen P.   Winter V.   Nyholm M.   Johansen B.N.   Olsen R.K.J.   Corydon M.J.   Andresen B.S.   Eiberg H.   Kølvraa S.   Gregersen N.  

Molecular Genetics and Metabolism, Vol. 67, Iss. 2, 1999-06 ,pp. : 138-147

Academic Press

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