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Inherited monogenic defects of ceramide metabolism: Molecular bases and diagnoses.
Dubot, Patricia; Sabourdy, Frédérique; Rybova, Jitka; Medin, Jeffrey A; Levade, Thierry.
Affiliation
  • Dubot P; Laboratoire de Biochimie Métabolique, Centre de Référence en Maladies Héréditaires du Métabolisme, Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France; INSERM UMR1037, CRCT (Cancer Research Center of Toulouse), Université Paul Sabatier, Toulouse, France.
  • Sabourdy F; Laboratoire de Biochimie Métabolique, Centre de Référence en Maladies Héréditaires du Métabolisme, Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France; INSERM UMR1037, CRCT (Cancer Research Center of Toulouse), Université Paul Sabatier, Toulouse, France.
  • Rybova J; Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Medin JA; Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, USA; Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: jmedin@mcw.edu.
  • Levade T; Laboratoire de Biochimie Métabolique, Centre de Référence en Maladies Héréditaires du Métabolisme, Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France; INSERM UMR1037, CRCT (Cancer Research Center of Toulouse), Université Paul Sabatier, Toulouse, France. Electronic address: thierry.lev
Clin Chim Acta ; 495: 457-466, 2019 Aug.
Article in En | MEDLINE | ID: mdl-31128082
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ceramides / Metabolic Diseases Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Clin Chim Acta Year: 2019 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ceramides / Metabolic Diseases Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Clin Chim Acta Year: 2019 Document type: Article Affiliation country: Country of publication: