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Neuroimage|September 20, 2011
Manual dexterity correlating with right lobule VI volume in right-handed 14-year-oldsSimone Kühn, Alexander Romanowski, Christina Schilling, et al.Brain : a Journal of Neurology|August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patientsM Anheim, B Monga, M Fleury, et al.Human Brain Mapping|November 15, 2011
Common structural correlates of trait impulsiveness and perceptual reasoning in adolescenceChristina Schilling, Simone Kühn, Alexander Romanowski, et al.Psychological Medicine|March 31, 2015
Resilience and corpus callosum microstructure in adolescenceA Galinowski, R Miranda, H Lemaitre, et al.Nature Genetics|February 11, 2004
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2Maria-Céu Moreira, Sandra Klur, Mitsunori Watanabe, et al.Nature Genetics|January 17, 2012
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the ciliumJi Eun Lee, Jennifer L Silhavy, Maha S Zaki, et al.Neurology|October 19, 2012
FXTAS: new insights and the need for revised diagnostic criteriaEmmanuelle Apartis, Anne Blancher, Wassilios G Meissner, et al.The Lancet. Diabetes & Endocrinology|October 16, 2021
Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort studyFanny Chasseloup, Isabelle Bourdeau, Antoine Tabarin, et al.New Directions for Child and Adolescent Development|September 22, 2020
Manifesto for new directions in developmental scienceBaptiste Barbot, Sascha Hein, Christopher Trentacosta, et al.Journal of Endocrinological Investigation|May 22, 2026
Addison's disease in Italy: mortality and survival by etiologyCarlotta Keiko Vedolin, Chiara Sabbadin, Alessandro Mondin, et al.Pageof 59