RANIERI, MICHELA

RANIERI, MICHELA  

Universita' degli Studi di MILANO  

Mostra records
Risultati 1 - 17 di 17 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A splicing site OPA1 mutation associated with autosomal dominant optic atrophy in an Italian family 1-gen-2010 M. RanieriR. Del BoS. CortiA. BordoniN. BresolinG.P. Comi + Conference Object -
Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases 28-apr-2014 G. RiboldiM. RanieriM. NizzardoC. SimoneF. MagriN. BresolinG.P. ComiS. Corti + Article (author) -
C9ORF72 hexanucleotide repeat expansion in a Cohort of Italian patients affected by Amyotrophic Lateral Sclerosis with and without frontotemporal dementia 1-gen-2012 R. Del BoS. CortiG. RiboldiM. RanieriC. FenoglioD. GalimbertiE. ScarpiniN. BresolinG. Comi Article (author) -
C9ORF72 repeat expansion in a large Italian ALS cohort : evidence of a founder effect 1-ott-2012 A. RattiR. Del BoC. TilocaM. RanieriS.P. CortiN. TicozziG.P. ComiV. Silani + Article (author) -
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 1-mag-2011 M. RanieriD. RonchiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RipoloneS. CortiP. VeggiottiG.P. Comi + Article (author) -
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 1-gen-2011 D. RonchiA. CosiA. BordoniV. LucchiniF. FortunatoE. FassoneD. TondutiM. RanieriM. RipoloneS. CortiP. VeggiottiG.P. Comi + Conference Object -
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant 1-ott-2012 A. BersanoM. RanieriC. CinnanteS. LanfranconiL. CandeliseI. GhioneE. BallabioN. Bresolin + Article (author) -
Contribution of FUS gene to FTLD-ALS spectrum: a genetic study in an Italian color of 484 patients 1-gen-2010 R. Del BoS. CortiM. RanieriD. SantoroN. BresolinG.P. Comi + Conference Object -
Guillain-Barre syndrome after rtPA therapy for acute stroke 1-gen-2010 A. BersanoD. SantoroS. LanfranconiM. RanieriN. Bresolin + Article (author) -
Mitochondrial fusion proteins and human diseases 1-gen-2013 M. RanieriG. RiboldiD. RonchiF. RizzoN. BresolinS. CortiG.P. Comi + Article (author) -
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 7-feb-2013 D. RonchiA. BordoniE. FassoneS. PagliaraniM. RanieriF. MagriL. PeverelliS. CortiN. BresolinG.P. Comi + Article (author) -
Next-generation sequeencing discloses DGUOK mutations in adult patients with mtDNA multiple deletions 1-gen-2013 D. RonchiA. BordoniM. RanieriF. MagriS. CortiN. BresolinG.P. Comi + Article (author) -
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 1-nov-2012 D. RonchiA. BordoniM. RipoloneM. RanieriF. MagriS. CortiN. BresolinG.P. Comi + Article (author) -
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort 1-giu-2011 S. CortiD. SantoroI. GhioneC. FenoglioM. RanieriD. GalimbertiE. ScarpiniN. BresolinG. Comi + Article (author) -
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families 15-apr-2012 M. RanieriR. Del BoA. BordoniD. RonchiI. ColomboG. RiboldiA. CosiF. MagriN. BresolinG.P. ComiS. Corti + Article (author) -
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia 1-mag-2013 N. TicozziR. Del BoC. FenoglioG. LauriaS. CortiD. GalimbertiM. RanieriE. ScarpiniG.P. ComiA. RattiV. Silani + Article (author) -
Tyr78Phe Transthyretin Mutation with Predominant Motor Neuropathy as the Initial Presentation 23-feb-2011 R. Del BoM. RanieriF. MagriN. BresolinS. CortiG.P. Comi + Article (author) -