Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lauren Fleming"'
Publikováno v:
Advances in Drug and Alcohol Research, Vol 3 (2023)
Introduction: With an estimated prevalence of up to five percent in the general population, fetal alcohol spectrum disorders (FASD) are the most common neurodevelopmental disorder and more prevalent than autism. Early identification and subsequent ea
Externí odkaz:
https://doaj.org/article/e2feec7996b0478d98e1cb2cbdd54758
Autor:
Garrett A. Stone, Hannah Wells, Samantha L. Stevenson, Lauren N. Duffy, Lauren Fleming, Jasmine Townsend, Maddie Nance
Publikováno v:
Therapeutic Recreation Journal. 53:224-243
There is limited research surrounding the effectiveness of program implementation, and the research that does exist often considers culture as a minor contributing factor. In this study, culture is re-framed as a major contributing factor of program
Autor:
Andrés J. García, Dennis W. Zhou, Manuel Salmerón-Sánchez, Tom Van Agtmael, Yinhui Lu, Lauren Fleming, Elie Ngandu Mpoyi, Karl E. Kadler, Yuan Yan Sin, Marco Cantini, Mercedes Costell
Publikováno v:
Biomaterials
Basement membranes (BMs) are specialised extracellular matrices that provide structural support to tissues as well as influence cell behaviour and signalling. Mutations in COL4A1/COL4A2, a major BM component, cause a familial form of eye, kidney and
Autor:
Elisabeth Tournier-Lasserve, Gregor Kuhlenbäumer, Eric Manchon, Françoise Bergametti, Christian Hagel, Clémence Jacquet, Carol Prieto-Morin, Françoise Chapon, Sophie Rosenstingl, Isabelle Girard-Buttaz, Hassan Hosseini, Hugues Chabriat, Dominique Hervé, Typhaine Morvan, Elena Leca-Radu, Charlotte Cordonnier, Tom Van Agtmael, Didier Goux, Alexandre Mackowiak, Lauren Fleming, Edgard Verdura
Publikováno v:
Annals of Neurology
Annals of Neurology, Wiley, 2016, 80 (5), pp.741-753. ⟨10.1002/ana.24782⟩
Annals of Neurology, 2016, 80 (5), pp.741-753. ⟨10.1002/ana.24782⟩
Annals of Neurology, Wiley, 2016, 80 (5), pp.741-753. ⟨10.1002/ana.24782⟩
Annals of Neurology, 2016, 80 (5), pp.741-753. ⟨10.1002/ana.24782⟩
International audience; OBJECTIVE: Cerebral small vessel disease (cSVD) is a heterogeneous group of disorders. Screening of known cSVD genes identifies the causative mutation in METHODS: We used linkage analysis and exome sequencing to identify the c