RIGON, LAURA

RIGON, LAURA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation 2011 BUSOLIN, GIORGIALEONARDI EVITIELLO, LIBERORIGON, LAURATOSATTO, SILVIO + NEUROLOGY - -
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy. 2011 RIGON, LAURAVETTORI, ANDREABUSOLIN, GIORGIA + EPILEPSY RESEARCH AND TREATMENT - Epilepsy research and treatment
A GENOMIC DELETION SPANNING PART OF LGI1 ASSOCIATED WITH AUTOSOMAL DOMINANT LATERAL TEMPORAL EPILEPSY 2011 RIGON, LAURA + EPILEPSIA - -
RNA-seq Transcriptome Profiling Of Primary Hunter Cells Following Treatment With Recombinant IDS As A First Step For Identification Of ERT Efficacy Markers 2011 SCARPA, MAURIZIOZANETTI, ALESSANDRAD'AVANZO, FRANCESCASALVALAIO, MARIKARIGON, LAURACAMPANARO, STEFANOVALLE, GIORGIOTOMANIN, ROSELLA + MOLECULAR GENETICS AND METABOLISM - Molecular Genetics and Metabolism
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 2012 RIGON, LAURARAMPAZZO, ALESSANDRA + NEUROLOGY - -
Circadian transcriptome analysis in human fibroblasts from Hunter syndrome and impact of iduronate-2-sulfatase treatment 2013 TOMANIN, ROSELLAD'AVANZO, FRANCESCASALVALAIO, MARIKARIGON, LAURAZANETTI, ALESSANDRASCARPA, MAURIZIO + BMC MEDICAL GENOMICS - BMC Medical Genomics
BBB Crossing in Lysosomal Storage Disorders: A Nanoparticle-Based Approach 2014 RIGON, LAURASALVALAIO, MARIKAD'AVANZO, FRANCESCASCARPA, MAURIZIOTOMANIN, ROSELLA + JOURNAL OF INBORN ERRORS OF METABOLISM AND SCREENING - -
Nanotechnologies for CNS drug delivery: therapy for the neurological compartment in the Mucopolisaccharidoses 2015 Rigon, Laura - - -
Targeted Polymeric Nanoparticles for Brain Delivery of High Molecular Weight Molecules in Lysosomal Storage Disorders 2016 RIGON, LAURAD'AVANZO, FRANCESCAMARIN, ORIANOSCARPA, MAURIZIOTOMANIN, ROSELLA + PLOS ONE - -
FGF signaling deregulation is associated with early developmental skeletal defects in animal models for mucopolysaccharidosis type II (MPSII). 2018 Bellesso StefaniaSalvalaio MarikaCosta RobertoBraghetta PaolaGiraudo ChiaraStramare RobertoRigon LauraTomanin RosellaMoro Enrico + HUMAN MOLECULAR GENETICS ONLINE - -
Molecular diagnosis of patients affected by mucopolysaccharidosis: a multicenter study 2019 Zanetti A.D'Avanzo F.Rigon L.Rampazzo A.Scarpa M.Tomanin R. + EUROPEAN JOURNAL OF PEDIATRICS - -
Mucopolysaccharidosis type II: One hundred years of research, diagnosis, and treatment 2020 Dʹavanzo F.Rigon L.Zanetti A.Tomanin R. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
Drosophila d-idua reduction mimics mucopolysaccharidosis type i disease-related phenotypes 2022 De Filippis C.Napoli B.Rigon L.Guarato G.Tomanin R.Orso G. + CELLS - -