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Journal of Child Neurology|July 19, 2012
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent featuresDavide Tonduti, Adeline Vanderver, Angela Berardinelli, et al.
Cytotherapy|November 12, 2009
Phenotypical/functional characterization of in vitro-expanded mesenchymal stromal cells from patients with Crohn's diseaseMaria Ester Bernardo, Maria Antonia Avanzini, Rachele Ciccocioppo, et al.
Hypertension (Dallas, Tex. : 1979)|December 13, 2017
Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common AncestorLuca Pagani, Yoan Diekmann, Marco Sazzini, et al.
Human Pathology|August 4, 2009
High-resolution genome-wide array comparative genomic hybridization in splenic marginal zone B-cell lymphomaFrancesca Novara, Luca Arcaini, Michele Merli, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletionsMaria C Bonaglia, Susan Marelli, Francesca Novara, et al.
Critical Pathways in Cardiology|November 12, 2020
The FAST-STEMI Network in Biella From 2013 to 2019: Impact of the Delocalization of the Hospital Facilities on Ischemia Time and In-hospital OutcomesMonica Verdoia, Orazio Viola, Giuseppina D'Amico, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 13, 2014
TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophyJacopo C DiFrancesco, Francesca Novara, Orsetta Zuffardi, et al.
Blood|September 9, 2011
Twenty-one cases of blastic plasmacytoid dendritic cell neoplasm: focus on biallelic locus 9p21.3 deletionMarco Lucioni, Francesca Novara, Giacomo Fiandrino, et al.
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