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American Journal of Medical Genetics. Part A|January 17, 2012
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex"Marco Castori, Oronzo Scarciolla, Silvia Morlino, et al.
Microbiome|August 14, 2022
Analysis of the anaerobic digestion metagenome under environmental stresses stimulating prophage inductionAlessandro Rossi, Maria Silvia Morlino, Maria Gaspari, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Late diagnosis of lateral meningocele syndrome in a 55-year-old woman with symptoms of joint instability and chronic musculoskeletal painMarco Castori, Silvia Morlino, Marco Ritelli, et al.
Computational and Structural Biotechnology Journal|April 15, 2022
KEMET - A python tool for KEGG Module evaluation and microbial genome annotation expansionMatteo Palù, Arianna Basile, Guido Zampieri, et al.
American Journal of Medical Genetics. Part A|March 8, 2017
Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility typeSilvia Morlino, Chiara Dordoni, Isabella Sperduti, et al.
Biotechnology Advances|September 29, 2023
Cupriavidus necator as a platform for polyhydroxyalkanoate production: An overview of strains, metabolism, and modeling approachesMaria Silvia Morlino, Rebecca Serna García, Filippo Savio, et al.
Chemosphere|February 14, 2022
Valorization of household food wastes to lactic acid production: A response surface methodology approach to optimize fermentation processChrysa Anagnostopoulou, Konstantinos N Kontogiannopoulos, Maria Gaspari, et al.
American Journal of Medical Genetics. Part A|November 21, 2013
Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility typeMarco Castori, Silvia Morlino, Claudia Celletti, et al.
American Journal of Medical Genetics. Part A|October 15, 2016
Ehlers-Danlos syndrome with lethal cardiac valvular dystrophy in males carrying a novel splice mutation in FLNAMarco Ritelli, Silvia Morlino, Edoardo Giacopuzzi, et al.
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