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Sara Morais

Showing results (41-50 of 49) with videos related to

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Plos One|December 4, 2020
αIIbβ3 variants in ten families with autosomal dominant macrothrombocytopenia: Expanding the mutational and clinical spectrumSara Morais, Jorge Oliveira, Catarina Lau, et al.
The EMBO Journal|May 6, 2018
<i>In vivo</i> expansion of functionally integrated GABAergic interneurons by targeted increase in neural progenitorsRachel E Shaw, Benjamin Kottler, Zoe N Ludlow, et al.
Advances in Experimental Medicine and Biology|December 8, 2017
Rare Neurodegenerative Diseases: Clinical and Genetic UpdateAntoni Matilla-Dueñas, Marc Corral-Juan, Agustí Rodríguez-Palmero Seuma, et al.
Artificial Intelligence in Medicine|October 2, 2023
Fair and equitable AI in biomedical research and healthcare: Social science perspectivesRenate Baumgartner, Payal Arora, Corinna Bath, et al.
Annals of Medicine|April 17, 2019
Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencingJose María Bastida, Sara Morais, Veronica Palma-Barqueros, et al.
Neurogenetics|January 24, 2021
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlationsJean-Loup Méreaux, Cristina Firanescu, Giulia Coarelli, et al.
Brain : a Journal of Neurology|May 31, 2015
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegiaMarie Coutelier, Cyril Goizet, Alexandra Durr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 11, 2025
American College of Rheumatology Guidance Statement for Diagnosis and Management of VEXAS Developed by the International VEXAS Working Group Expert PanelArsene M Mekinian, Sophie Georgin-Lavaille, Marcela A Ferrada, et al.
Blood|July 22, 2020
Novel manifestations of immune dysregulation and granule defects in gray platelet syndromeMatthew C Sims, Louisa Mayer, Janine H Collins, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Plos One|December 4, 2020
αIIbβ3 variants in ten families with autosomal dominant macrothrombocytopenia: Expanding the mutational and clinical spectrumSara Morais, Jorge Oliveira, Catarina Lau, et al.
The EMBO Journal|May 6, 2018
<i>In vivo</i> expansion of functionally integrated GABAergic interneurons by targeted increase in neural progenitorsRachel E Shaw, Benjamin Kottler, Zoe N Ludlow, et al.
Advances in Experimental Medicine and Biology|December 8, 2017
Rare Neurodegenerative Diseases: Clinical and Genetic UpdateAntoni Matilla-Dueñas, Marc Corral-Juan, Agustí Rodríguez-Palmero Seuma, et al.
Artificial Intelligence in Medicine|October 2, 2023
Fair and equitable AI in biomedical research and healthcare: Social science perspectivesRenate Baumgartner, Payal Arora, Corinna Bath, et al.
Annals of Medicine|April 17, 2019
Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencingJose María Bastida, Sara Morais, Veronica Palma-Barqueros, et al.
Neurogenetics|January 24, 2021
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlationsJean-Loup Méreaux, Cristina Firanescu, Giulia Coarelli, et al.
Brain : a Journal of Neurology|May 31, 2015
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegiaMarie Coutelier, Cyril Goizet, Alexandra Durr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 11, 2025
American College of Rheumatology Guidance Statement for Diagnosis and Management of VEXAS Developed by the International VEXAS Working Group Expert PanelArsene M Mekinian, Sophie Georgin-Lavaille, Marcela A Ferrada, et al.
Blood|July 22, 2020
Novel manifestations of immune dysregulation and granule defects in gray platelet syndromeMatthew C Sims, Louisa Mayer, Janine H Collins, et al.
Pageof 5