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Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5.
Marelli, Cecilia; Lamari, Foudil; Rainteau, Dominique; Lafourcade, Alexandre; Banneau, Guillaume; Humbert, Lydie; Monin, Marie-Lorraine; Petit, Elodie; Debs, Rabab; Castelnovo, Giovanni; Ollagnon, Elisabeth; Lavie, Julie; Pilliod, Julie; Coupry, Isabelle; Babin, Patrick J; Guissart, Claire; Benyounes, Imen; Ullmann, Urielle; Lesca, Gaetan; Thauvin-Robinet, Christel; Labauge, Pierre; Odent, Sylvie; Ewenczyk, Claire; Wolf, Claude; Stevanin, Giovanni; Hajage, David; Durr, Alexandra; Goizet, Cyril; Mochel, Fanny.
Affiliation
  • Marelli C; Gui de Chauliac University Hospital, Department of Neurology, Montpellier, France.
  • Lamari F; Gui de Chauliac University Hospital, Expert Center for Neurogenetic Diseases and Adult Mitochondrial and Metabolic Diseases, Montpellier, France.
  • Rainteau D; APHP, La Pitié-Salpêtrière University Hospital, Department of Biochemistry, Paris, France.
  • Lafourcade A; University Pierre and Marie Curie, Neurometabolic Research Group, Paris, France.
  • Banneau G; APHP, La Pitié-Salpêtrière University Hospital, Reference Center for Adult Neurometabolic Diseases, Paris, France.
  • Humbert L; APHP, Hôpital Saint Antoine, Département PM2 Plateforme de Métabolomique, Peptidomique et dosage de Médicaments, Paris, France.
  • Monin ML; APHP, Hôpital La Pitié-Salpêtrière, Département de Biostatistiques, Santé publique et Information médicale, Centre de Pharmacoépidémiologie (Cephepi), F-75013, Paris, France.
  • Petit E; APHP, La Pitié-Salpêtrière University Hospital, Department of Genetics, Functional Unit of Molecular and Cellular Neurogenetics, Paris, France.
  • Debs R; APHP, Hôpital Saint Antoine, Département PM2 Plateforme de Métabolomique, Peptidomique et dosage de Médicaments, Paris, France.
  • Castelnovo G; APHP, La Pitié-Salpêtrière University Hospital, Department of Genetics, Paris, France.
  • Ollagnon E; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
  • Lavie J; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
  • Pilliod J; APHP, La Pitié-Salpêtrière University Hospital, Department of Neurology, Paris, France.
  • Coupry I; Caremeau University Hospital, Department of Neurology, Nimes, France.
  • Babin PJ; La Croix-Rousse University Hospital, Department of Genetics, Lyon, France.
  • Guissart C; Laboratoire MRGM, INSERM U1211, Univ Bordeaux, Bordeaux, France.
  • Benyounes I; Laboratoire MRGM, INSERM U1211, Univ Bordeaux, Bordeaux, France.
  • Ullmann U; Laboratoire MRGM, INSERM U1211, Univ Bordeaux, Bordeaux, France.
  • Lesca G; Laboratoire MRGM, INSERM U1211, Univ Bordeaux, Bordeaux, France.
  • Thauvin-Robinet C; Institut Universitaire de Recherche Clinique, Laboratoire de Génétique Moléculaire, Montpellier, France.
  • Labauge P; APHP, La Pitié-Salpêtrière University Hospital, Department of Biochemistry, Paris, France.
  • Odent S; Institut de Pathologie et Génétique, Centre de Génétique Humaine, Gosselies, Belgium.
  • Ewenczyk C; Lyon University Hospital, Department of Medical Genetics, Lyon, France.
  • Wolf C; Dijon University Hospital, Department of Genetics, Dijon, France.
  • Stevanin G; Gui de Chauliac University Hospital, Department of Neurology, Montpellier, France.
  • Hajage D; Gui de Chauliac University Hospital, Reference Center for Adult Leukodystrophy, Montpellier, France.
  • Durr A; Rennes University Hospital, Department of Clinical Genetics, Rennes, France.
  • Goizet C; APHP, La Pitié-Salpêtrière University Hospital, Department of Genetics, Paris, France.
  • Mochel F; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
Brain ; 141(1): 72-84, 2018 01 01.
Article in En | MEDLINE | ID: mdl-29228183
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Oxysterols / Anticholesteremic Agents / Mutation Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Infant / Male / Middle aged Language: En Journal: Brain Year: 2018 Document type: Article Affiliation country: France Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Oxysterols / Anticholesteremic Agents / Mutation Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Infant / Male / Middle aged Language: En Journal: Brain Year: 2018 Document type: Article Affiliation country: France Country of publication: United kingdom