MOSCA, LORENA

MOSCA, LORENA  

Universita' degli Studi di MILANO  

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Risultati 1 - 10 di 10 (tempo di esecuzione: 0.017 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Analysis of red cell membrane proteins by capillary gel electrophoresis 2008 L. MoscaA. MoscaR. Paleari Article (author) -
Analysis of red cell membrane proteins by capillary gel electrophoresis 2008 L. Mosca Working Paper -
Applicazioni dell'elettroforesi capillare all'analisi delle proteine della membrana eritrocitaria 2009 MOSCA, LORENAR. PaleariA. Mosca Article (author) -
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort. 2020 Scarlino SPozzi LRomano AMosca LPenco SSansone VFazio R + Article (author) -
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations 2012 L. MoscaS. PileggiF. AvemariaC. TarlariniCIGOLI, MARIA SOLE + Article (author) -
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression 2011 F. AvemariaC. TarlariniL. Mosca + Article (author) -
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease 2011 L. MoscaF. AvemariaC. Tarlarini + Article (author) -
Posture and visual system : the role of phoria 2008 W. AlbisettiS. SimonettaM. PirasL. MoscaR. Ratiglia + Article (author) -
Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency 2022 Calabresi, LauraPavanello, ChiaraMosca, Lorena + Article (author) -
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject 2012 L. MoscaC. TarlariniF. Avemaria + Article (author) -