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Publications by Cui Y

Clinical Diagnosis and Treatment of 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency in One Infant: A Case Report

Medical Reports & Case Studies

English

Related publications

Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

English

Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

Journal of Inherited Metabolic Disease

English

Glutaryl-CoA Dehydrogenase Deficiency

English

Outcome of Medium Chain Acyl-CoA Dehydrogenase Deficiency After Diagnosis

Archives of Disease in Childhood

English

Hyperinsulinism Due to Short Chain 3-Hydroxylacyl-CoA Dehydrogenase Deficiency

English

Diagnosis of Medium Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency in an Asymptomatic Neonate

Annals of Clinical Biochemistry

Clinical Biochemistry

English

Short Chain Acyl-CoA Dehydrogenase Deficiency

English

Poly(3-Hydroxybutyrate) Degradation in Ralstonia Eutropha H16 Is Mediated Stereoselectively to (S)-3-Hydroxybutyryl Coenzyme a (CoA) via Crotonyl-CoA

Journal of Bacteriology

Molecular Biology

English

Intraventricular Baclofen for Treatment of Severe Dystonia Associated With Glutaryl-CoA Dehydrogenase Deficiency (GA1): Report of Two Cases

Movement Disorders Clinical Practice

English