Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Samantha Caillet"'
Autor:
Elodie Hainque, Samantha Caillet, Sandrine Leroy, Constance Flamand-Roze, Isaac Adanyeguh, Fanny Charbonnier-Beaupel, Maryvonne Retail, Benjamin Le Toullec, Mariana Atencio, Sophie Rivaud-Péchoux, Vanessa Brochard, Florence Habarou, Chris Ottolenghi, Florence Cormier, Aurélie Méneret, Marta Ruiz, Mohamed Doulazmi, Anne Roubergue, Jean-Christophe Corvol, Marie Vidailhet, Fanny Mochel, Emmanuel Roze
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Abstract Background Based on the hypothesis of a brain energy deficit, we investigated the safety and efficacy of triheptanoin on paroxysmal episodes in patients with alternating hemiplegia of childhood due to ATP1A3 mutations. Methods We conducted a
Externí odkaz:
https://doaj.org/article/a99b74495ac847fd9ca2c7591eb1311f
Autor:
Alexandra Dürr, Pierre-Gilles Henry, Isaac M. Adanyeguh, Romain Valabregue, Daisy Rinaldi, Fanny Mochel, Samantha Caillet
Publikováno v:
Neurology. 84:490-495
Objective: Based on our previous work in Huntington disease (HD) showing improved energy metabolism in muscle by providing substrates to the Krebs cycle, we wished to obtain a proof-of-concept of the therapeutic benefit of triheptanoin using a functi
Autor:
Laurent Servais, Bénédicte Héron, Sandrine Vuillaumier, Elsa Kaphan, Domitille Gras, Emmanuel Roze, Raphael Schiffmann, Romain Valabregue, Elodie Hainque, Samantha Caillet, Chris Ottolenghi, Isaac M. Adanyeguh, Agathe Roubertie, Fanny Mochel, Jean-Yves Hogrel, Daisy Rinaldi
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 2016, 87 (5), pp.550-553. ⟨10.1136/jnnp-2015-311475⟩
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2016, 87 (5), pp.550-553. 〈10.1136/jnnp-2015-311475〉
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2016, 87 (5), pp.550-553. ⟨10.1136/jnnp-2015-311475⟩
Journal of Neurology, Neurosurgery, and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 2016, 87 (5), pp.550-553. ⟨10.1136/jnnp-2015-311475⟩
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2016, 87 (5), pp.550-553. 〈10.1136/jnnp-2015-311475〉
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2016, 87 (5), pp.550-553. ⟨10.1136/jnnp-2015-311475⟩
Journal of Neurology, Neurosurgery, and Psychiatry
Objective:On the basis of our previous work with triheptanoin, which provides key substrates to the Krebs cycle in the brain, we wished to assess its therapeutic effect in patients with glucose transporter type 1 deficiency syndrome (GLUT1-DS) who ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a14b7fc1b453e76eb7aba1c2fec7cd5
https://hal.sorbonne-universite.fr/hal-01325371
https://hal.sorbonne-universite.fr/hal-01325371
Autor:
A Roubergue, Mariana Atencio, Marta Ruiz, Aurélie Méneret, Vanessa Brochard, Maryvonne Retail, Samantha Caillet, Sandrine Leroy, Jean-Christophe Corvol, Emmanuel Roze, Elodie Hainque, Florence Habarou, Isaac Adanyeguh, Sophie Rivaud-Péchoux, Benjamin Le Toullec, Chris Ottolenghi, Constance Flamand-Roze, Fanny Mochel, Mohamed Doulazmi, Fanny Charbonnier-Beaupel, Marie Vidailhet, Florence Cormier
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2016, 12 (1), pp.160. ⟨10.1186/s13023-017-0713-2⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2016, 12 (1), pp.160. ⟨10.1186/s13023-017-0713-2⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2016, 12 (1), pp.160. 〈10.1186/s13023-017-0713-2〉
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Orphanet Journal of Rare Diseases, 2016, 12 (1), pp.160. ⟨10.1186/s13023-017-0713-2⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2016, 12 (1), pp.160. ⟨10.1186/s13023-017-0713-2⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2016, 12 (1), pp.160. 〈10.1186/s13023-017-0713-2〉
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
International audience; AbstractBackgroundBased on the hypothesis of a brain energy deficit, we investigated the safety and efficacy of triheptanoin on paroxysmal episodes in patients with alternating hemiplegia of childhood due to ATP1A3 mutations.M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f94fdc289e775fbac7bc7049087f74
https://www.hal.inserm.fr/inserm-01612741/document
https://www.hal.inserm.fr/inserm-01612741/document
Autor:
Romain Valabregue, Alexandra Durr, Samantha Caillet, Pierre-Gilles Henry, Isaac M. Adanyeguh, Daisy Rinaldi, Fanny Mochel
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 85:A103-A103
Background Energy deficit has been implicated in the pathophysiology of Huntington disease (HD). Our previous work indicated a possibility of improving energy deficit by providing substrates to the Krebs cycle using anaplerotic therapies. Aims Here o