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Clinical Genetics|February 6, 2016
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiencyN Bouali, B Francou, J Bouligand, et al.Annales D'Endocrinologie|April 6, 2010
Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and geneticsH Bry-Gauillard, S Trabado, J Bouligand, et al.European Journal of Neurology|August 7, 2020
Demyelinating Charcot-Marie-Tooth neuropathy associated with FBLN5 mutationsD Safka Brozkova, T Stojkovic, J Haberlová, et al.Nature|August 27, 2014
A major advance of tropical Andean glaciers during the Antarctic cold reversalV Jomelli, V Favier, M Vuille, et al.Revue Neurologique|April 20, 2024
Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009-2019)D Adams, P Cintas, G Solé, et al.Pageof 1