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Hereditary orotic aciduria with epilepsy and without megaloblastic anemia.
Grohmann, Karina; Lauffer, Heinz; Lauenstein, Peter; Hoffmann, Georg F; Seidlitz, Günter.
Affiliation
  • Grohmann K; Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital Greifswald, Greifswald, Germany.
  • Lauffer H; Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital Greifswald, Greifswald, Germany.
  • Lauenstein P; Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital Greifswald, Greifswald, Germany.
  • Hoffmann GF; Center for Child and Adolescent Medicine, Division of Inherited Metabolic Diseases, University Hospital Heidelberg, Heidelberg, Germany.
  • Seidlitz G; Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital Greifswald, Greifswald, Germany.
Neuropediatrics ; 46(2): 123-5, 2015 Apr.
Article in En | MEDLINE | ID: mdl-25757096
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Orotate Phosphoribosyltransferase / Orotic Acid / Orotidine-5'-Phosphate Decarboxylase / Epilepsy / Anemia, Megaloblastic / Metabolic Diseases / Multienzyme Complexes Limits: Child, preschool / Humans / Male Language: En Journal: Neuropediatrics Year: 2015 Document type: Article Affiliation country: Germany Country of publication: Germany
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Orotate Phosphoribosyltransferase / Orotic Acid / Orotidine-5'-Phosphate Decarboxylase / Epilepsy / Anemia, Megaloblastic / Metabolic Diseases / Multienzyme Complexes Limits: Child, preschool / Humans / Male Language: En Journal: Neuropediatrics Year: 2015 Document type: Article Affiliation country: Germany Country of publication: Germany