COSI, ALESSANDRA

COSI, ALESSANDRA  

Universita' degli Studi di MILANO  

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Risultati 1 - 9 di 9 (tempo di esecuzione: 0.008 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation :aA case report 1-gen-2011 D. RonchiA. CosiA. BordoniF. FortunatoP. 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. FassoneM. RanieriM. RipoloneS. CortiP. VeggiottiG.P. Comi + Conference Object -
Le mycophénolate mofétil en traitement d’induction et traitement d’entretien à long terme dans la prise en charge de la vascularite primitive du système nerveux central chez l’enfant 1-gen-2018 Cosi, AlessandraCimaz, Rolando + Article (author) -
Long-Term Efficacy and Safety of Mycophenolate Mofetil in Childhood Primary Central Nervous System Vasculitis 1-gen-2015 Cosi, ACimaz, R + Article (author) -
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood : primary angiitis of the central nervous system 1-gen-2017 Cosi AlessandraCimaz Rolando + Article (author) -
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment 1-mar-2012 D. RonchiA. BordoniE. FassoneA. CosiM. ServidaS. CortiN. BresolinG. P. 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) -
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia 15-set-2011 D. RonchiE. FassoneA. BordoniV. LucchiniA. Di FonzoI. ColomboA. CosiS. CortiN. BresolinG.P. Comi + Article (author) -
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation 1-ago-2011 D. RonchiA. BordoniCOSI, ALESSANDRAE. FassoneA. Di FonzoM. ServidaV. LucchiniM. MattioliN. BresolinS. CortiG. Comi + Article (author) -