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Clinical Genetics|October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literatureC Nemos, L Lambert, F Giuliano, et al.Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, et al.Translational Psychiatry|June 14, 2017
The influence of the rs6295 gene polymorphism on serotonin-1A receptor distribution investigated with PET in patients with major depression applying machine learningA Kautzky, G M James, C Philippe, et al.Clinical Genetics|April 11, 2016
Rett-like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5-related diseaseL Allou, S Julia, D Amsallem, et al.Clinical Pharmacology and Therapeutics|March 5, 2016
Pilot PET Study to Assess the Functional Interplay Between ABCB1 and ABCG2 at the Human Blood-Brain BarrierM Bauer, K Römermann, R Karch, et al.Annales De Biologie Clinique|February 15, 2001
[Plasma homocysteine measurement: a study of pre-analytical variation factors for conditions for total plasma homocysteine concentration]V Ducros, M Candito, E Caussé, et al.Space Science Reviews|May 23, 2025
SMILE Modeling Working Group: Modeling and Analysis of X-ray and Ultraviolet Images of Solar Wind - Earth InteractionsHyunju K Connor, Tianran Sun, Andrey Samsonov, et al.Cerebral Cortex (New York, N.Y. : 1991)|December 3, 2016
Association of Protein Distribution and Gene Expression Revealed by PET and Post-Mortem Quantification in the Serotonergic System of the Human BrainA Komorowski, G M James, C Philippe, et al.Science Advances|March 2, 2019
Direct evidence of nonstationary collisionless shocks in space plasmasAndrew P Dimmock, Christopher T Russell, Roald Z Sagdeev, et al.Pageof 25