LAMPERTI, COSTANZA

LAMPERTI, COSTANZA  

Universita' degli Studi di MILANO  

Mostra records
Risultati 1 - 20 di 100 (tempo di esecuzione: 0.001 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy 2005 A. BordoniM.CrimiA. Di FonzoC. LampertiN. BresolinG.P. Comi + Article (author) -
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD 2008 C. LampertiV. CrugnolaM. ServidaF. FortunatoA. Di FonzoG. P. ComiN. Bresolin + Article (author) -
A mouse model of facioscapulohumeral muscular dystrophy 2005 C. LampertiV. LucchiniC. ZeccaN. Bresolin + Book Part (author) -
A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy 2017 C. LampertiGHEZZI, DANIELE + Article (author) -
A novel homozygous mutation in SUCLA2 gene identified by exome sequencing 2012 Lamperti C.Ghezzi D. + Article (author) -
Adult Form Type II Glycogen Storage Disease in a Northern Italy Population : Phenotype Characterization, Early Diagnosis and Prognostic Determinants 2009 D. RonchiC. LampertiA. BordoniF. MagriN. BresolinG. P. Comi + Article (author) -
Adult form type II Glycogen Storage Disease in a Northern Italy population :_phenotype, charatcerization, early diagnosis and prognostic determinants 2008 D. RonchiC. LampertiM.G. D'AngeloA. BordoniF. MagriN. BresolinG.P. Comi + Article (author) -
Autologous Transplantation of Ac133+ stem cells in Duchenne Muscular Dystrophy 2005 Y. TorrenteM. BelicchiC. MarchesiM. GavinaC. Lamperti + Book Part (author) -
Autologous transplantation of AC133+ stem cells in Duchenne muscular Dystrophy : preclinical and clinical evidences 2005 Y. TorrenteM. BelicchiC. LampertiG.P. ComiN. StocchettiA. PrioriG. CossuN. Bresolin + Article (author) -
Autologous transplantation of AC133+ stem cells in Duchenne muscular Dystrophy : preclinical and clinical evidences 2005 Y. TorrenteM. BelicchiC. MarchesiM. GavinaC. Lamperti + Book Part (author) -
Autosomal dominant and recessive limb-girdle muscular dystrophies : clinical, genetic relative frequency in a large Italian population 2007 M. GuglieriF. MagriR. CaglianiF. FortunatoS. LucchiariS. SalaniR. Del BoC. ZeccaC. LampertiN. BresolinG.P. Comi + Article (author) -
Autosomal dominant and recessive limb-girdle muscular dystrophies: relative frequency in a large Italian population 2005 M.GuglieriF. MagriF. FortunatoS. LucchiariR. Del BoA. BordoniC. ZeccaC. LampertiN. BresolinG.P. Comi + Article (author) -
Autosomal Recessive Ala93Thr mutation in caveolin-3 gene : a new family 2008 F.M.B. MagriC. LampertiD. RonchiE. FassoneN. BresolinG.P. Comi + Article (author) -
Bank of DNA, cell lines and nerve-muscle-cardiac tissues 2005 C. LampertiC. ZeccaM.E. FrugugliettiV. LucchiniG.P. ComiA. BordoniF. FortunatoY. Torrente + Book Part (author) -
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement 2022 Lamperti, CostanzaGhezzi, Daniele + Article (author) -
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia 2021 Nasca A.Lamperti C.Ghezzi D. + Article (author) -
Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions 2022 Nasca A.Meneri M.Comi G. P.Catania A.Lamperti C.Ronchi D.Ghezzi D. + Article (author) -
Clinical and genetic heterogeneity of dysferlin deficiency 2005 F. MagriR. Del BoF. FortunatoC. LampertiS. LucchiariN. BresolinG.P. Comi + Book Part (author) -
Clinical and genetical variability in a large sample of LGMD Italian patients 2007 F. MagriM. GuglieriM. D’AngeloR. CaglianiR. Del BoD. RonchiC. LampertiF. FortunatoN. BresolinG.P.Comi + Conference Object -
Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene 2007 R. Del BoC. LampertiN. BresolinE. BallabioL. CandeliseG.P. ComiS. Corti + Conference Object -