SERVIDA, MAURA

SERVIDA, MAURA  

Universita' degli Studi di MILANO  

Risultati 1 - 17 di 17 (tempo di esecuzione: 0.167 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Cephalalgia, myopathy and familial dementia with CADASIL-like MRI and multiple mtDNA deletions 1-gen-2008 M. ServidaD. RonchiA. BordoniG. ComiN. Bresolin + Conference Object -
Cephalalgia, myopathy and familial dementia with CADASIL-like MRI and multiple mtDNA deletions 1-giu-2008 M. ServidaD. RonchiA. BordoniG.P. ComiN. Bresolin + Article (author) -
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient 1-ott-2013 S. LucchiariG. UlziF. MagriM. BucchiaM. ServidaG.P. Comi + Article (author) -
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene 1-giu-2008 D. RonchiA. BordoniR. VirgilioE. FassoneA. DiFonzoM. ServidaV. LucchiniM. MatteoliN. BresolinG.P. Comi + Article (author) -
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion 15-dic-2008 S. LucchiariS. PagliaraniS.P. CortiE. MancinelliM. ServidaM.E. FrugugliettiV. SansoneN. BresolinG.P. ComiG. Meola + Article (author) -
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy. 1-giu-2009 V. LucchiniV. CrugnolaM. ServidaA. BordoniD. RonchiN. BresolinG.P. ComiY. Torrente + Conference Object -
Decline of ALS-FRS and Norris scale scores in a group of patients affected by ALS and treated with lithium 1-giu-2009 D. SantoroI. GhioneS. CortiM. ServidaN. BresolinG.P. Comi. + Conference Object -
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD 11-mar-2008 C. LampertiV. CrugnolaM. ServidaF. FortunatoA. Di FonzoG. P. ComiN. Bresolin + Article (author) -
Mitochondrial, Ehlers-Danlos and CADASIL features in the same family: a genetic puzzle or a new disease entità? 1-mag-2009 M. ServidaA. BordoniG.P. ComiA. BassottiM. ValliN. Bresolin + Conference Object -
Mitocondriapatia, Ehlers-Danlos, e CADASIL: coesistenza di caratteristiche delle tre patologie nella stessa famiglia. 1-gen-2009 M. ServidaA. BordoniG.P. ComiN. Bresolin + Conference Object -
Morphological pattern of muscle biopsy in a large cohort of FSHD patients 1-gen-2008 V. CrugnolaM. ServidaN. Bresolin + Conference Object -
mtDNA depletion in a case of fatal infant cytochrome c oxidase deficiency presenting with clinical feature of type 1 spinal muscular atrophy 1-gen-2008 V. LucchiniA. BordoniD. RonchiE. FassoneM. ServidaM. PluderiG.P. ComiN. Bresolin + Article (author) -
Myotonic dystrophy type 2: clinical, neurophysiological mnd muscular features of a family with short CCTG expansion. 1-gen-2007 S. LucchiariS. CortiS. PagliaraniM. ServidaE. FrugugliettiN. BresolinG.P. Comi + Conference Object -
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) -
Studio retrospettivo di biopsie muscolari di pazienti con possibile diagnosi di miopatia miofibrillare 1-giu-2009 M. ServidaM.E. FrugugliettiC. LampertiG.P. ComiN. Bresolin + Conference Object -
Survival gain in glioblastoma patients treated with dendritic cell immunotherapy is associated with increased NK but not CD8+ T cell activation in the presence of adjuvant temozolomide 1-gen-2018 Pellegatta, SerenaCuccarini, ValeriaServida, MauraAcerbi, FrancescoFerroli, PaoloDiMeco, Francesco + 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) -