Kolexia
Bourthoumieu Sylvie
Pharmacien
Hôpital Dupuytren
Limoges, France
54 Activités
25 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Neuropathies périphériques Maladie de Charcot-Marie-Tooth Maladies chromosomiques Maladies des dents Hyperalgésie Atrésie intestinale Délétion de segment de chromosome Syndrome de DiGeorge Aberrations des chromosomes

Industries

AstraZeneca
1 collaboration(s)
Dernière en 2021
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Dernières activités

Netazepide, an Antagonist of Cholecystokinin Type 2 Receptor, Prevents Vincristine-Induced Sensory Neuropathy in Mice.
Pharmaceuticals (Basel, Switzerland)   23 janvier 2024
Neuroprotective Effect of Polyvalent Immunoglobulins on Mouse Models of Chemotherapy-Induced Peripheral Neuropathy.
Pharmaceutics   20 janvier 2024
NETAZEPIDE, AN ANTAGONIST OF CHOLECYSTOKININ TYPE 2 RECEPTOR, PREVENTS PACLITAXEL-INDUCED SENSORY NEUROPATHY IN MICE
2023 PNS Annual Meeting – Copenhagen, 17‐20 June 2023   09 octobre 2023
Blockade of CCK2R prevents the onset of vincristine-induced sensory neuropathy in mice
Abstracts of the Annual Meeting of French Society of Pharmacology and Therapeutics, 12–14 June 2023, Limoges, France   07 juin 2023
Comparative analysis of histopathological parameters, genome-wide copy number alterations, and variants in genes involved in cell cycle regulation in chordomas of the skull base and sacrum.
Journal of neuropathology and experimental neurology   21 mars 2023
Hereditary predisposition to malignant myeloid hemopathies: Caution in use of saliva and guideline based on our experience.
Frontiers in oncology   27 février 2023
Blockade of Cholecystokinin Type 2 Receptors Prevents the Onset of Vincristine-Induced Neuropathy in Mice.
Pharmaceutics   16 décembre 2022
Follow-up of increased nuchal translucency: Results of a study of 398 cases.
Journal of gynecology obstetrics and human reproduction   06 octobre 2022
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases.
Journal of medical genetics   22 septembre 2022
GM2 gangliosidosis AB variant: first case of late onset and review of the literature.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology   04 août 2022