Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequenceGHEZZI, Daniele; VISCOMI, Carlo; FERLINI, Alessandra et al.Human molecular genetics (Print). 2009, Vol 18, Num 6, pp 1058-1064, issn 0964-6906, 7 p.Article

MACROPHAGES: A MINIMALLY INVASIVE TOOL FOR MONITORING COLLAGEN VI MYOPATHIESGUALANDI, Francesca; CURCI, Rosa; SABATELLI, Patrizia et al.Muscle & nerve. 2011, Vol 44, Num 1, pp 80-84, issn 0148-639X, 5 p.Article

Reducing transplant-related mortality after allogeneic hematopoietic stem cell transplantationBACIGALUPO, Andrea; SORMANI, Maria Pia; PIAGGIO, Giovanna et al.Haematologica (Roma). 2004, Vol 89, Num 10, pp 1238-1247, issn 0390-6078, 10 p.Article

Aspergillus galactomannan antigen in the cerebrospinal fluid of bone marrow transplant recipients with probable cerebral aspergillosisVISCOLI, Claudio; MACHETTI, Marco; GAZZOLA, Paola et al.Journal of clinical microbiology (Print). 2002, Vol 40, Num 4, pp 1496-1499, issn 0095-1137Article

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionVACCA, Marcella; FILIPPINI, Francesco; TRABANELLI, Cecilia et al.Brain & development (Tokyo. 1979). 2001, Vol 23, pp S246-S250, issn 0387-7604, SUP1Conference Paper

Expression of the Collagen VI α5 and α6 Chains in Normal Human Skin and in Skin of Patients with Collagen VI-Related MyopathiesSABATELLI, Patrizia; GARA, Sudheer K; PAULSSON, Mats et al.Journal of investigative dermatology. 2011, Vol 131, Num 1, pp 99-107, issn 0022-202X, 9 p.Article

Muscle Magnetic Resonance Imaging Involvement in Muscular Dystrophies with Rigidity of the SpineMERCURI, Eugenio; CLEMENTS, Emma; GUALANDI, Francesca et al.Annals of neurology. 2010, Vol 67, Num 2, pp 201-208, issn 0364-5134, 8 p.Article

Treatment of acute graft-versus-host disease with low-dose, alternate-day antithymocyte globulinGRAZIANI, Francesco; VAN LINT, Maria Teresa; BACIGALUPO, Andrea et al.Haematologica (Roma). 2002, Vol 87, Num 9, pp 973-978, issn 0390-6078Article

Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin geneTOFFOLATTI, Luisa; CARDAZZO, Barbara; FANIN, Marina et al.Genomics (San Diego, Calif.). 2002, Vol 80, Num 5, pp 523-530, issn 0888-7543, 8 p.Article

Transplant-related mortality and long-term graft function are significantly influenced by cell dose in patients undergoing allogeneic marrow transplantationDOMINIETTO, Alida; LAMPARELLI, Teresa; FRASSONI, Francesco et al.Blood. 2002, Vol 100, Num 12, pp 3930-3934, issn 0006-4971, 5 p.Article

Natural history of pulmonary function in collagen VI-related myopathiesFOLEY, A. Reghan; QUIJANO-ROY, Susana; NORTH, Kathryn et al.Brain. 2013, Vol 136, pp 3625-3633, issn 0006-8950, 9 p., 12Article

Galactomannan testing might be useful for early diagnosis of fusariosisMIKULSKA, Małgorzata; FURFARO, Elisa; VISCOLI, Claudio et al.Diagnostic microbiology and infectious disease. 2012, Vol 72, Num 4, pp 367-369, issn 0732-8893, 3 p.Article

REPEATED COURSES OF GRANULOCYTE COLONY-STIMULATING FACTOR IN AMYOTROPHIC LATERAL SCLEROSIS: CLINICAL AND BIOLOGICAL RESULTS FROM A PROSPECTIVE MULTICENTER STUDYCHIO, Adriano; MORA, Gabriele; CALVO, Andrea et al.Muscle & nerve. 2011, Vol 43, Num 2, pp 189-195, issn 0148-639X, 7 p.Article

Antisense Modulation of Both Exonic and Intronic Splicing Motifs Induces Skipping of a DMD Pseudo-Exon Responsible for X-Linked Dilated CardiomyopathyRIMESSI, Paola; FABRIS, Marina; FERLINI, Alessandra et al.Human gene therapy. 2010, Vol 21, Num 9, pp 1137-1146, issn 1043-0342, 10 p.Article

Autologous HSCT for severe progressive multiple sclerosis in a multicenter trial : impact on disease activity and quality of lifeSACCARDI, Riccardo; LUIGI MANCARDI, Gian; LA NASA, Giorgio et al.Blood. 2005, Vol 105, Num 6, pp 2601-2607, issn 0006-4971, 7 p.Article

Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationRIMESSI, Paola; GUALANDI, Francesca; DUPREZ, Laurence et al.American journal of medical genetics. 2005, Vol 132A, Num 4, pp 391-394, issn 0148-7299, 4 p.Article

Leukaemia relapse after allogeneic transplants for acute myeloid leukaemia: predictive role of WT1 expressionPOZZI, Sarah; GEROLDI, Simona; BREGANTE, Stefania et al.British journal of haematology. 2013, Vol 160, Num 4, pp 503-509, issn 0007-1048, 7 p.Article

Muscle Fiber Atrophy and Regeneration Coexist in Collagen VI―Deficient Human Muscle: Role of Calpain-3 and Nuclear Factor-κB SignalingPACO, Sonia; FERRER, Isidre; COLOMER, Jaume et al.Journal of neuropathology and experimental neurology. 2012, Vol 71, Num 10, pp 894-906, issn 0022-3069, 13 p.Article

Brody Disease: Insights Into Biochemical Features of SERCA1 and Identification of a Novel MutationVATTEMI, Gaetano; GUALANDI, Francesca; VAN KUPPEVELT, Toin H et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 3, pp 246-252, issn 0022-3069, 7 p.Article

Human mesenchymal stem cells modulate B-cell functionsCORCIONE, Anna; BENVENUTO, Federica; UCCELLI, Antonio et al.Blood. 2006, Vol 107, Num 1, pp 367-372, issn 0006-4971, 6 p.Article

Autologous stem cell transplantation as rescue therapy in malignant forms of multiple sclerosisMANCARDI, Giovanni Luigi; MURIALDO, Alessandra; COMI, Giancarlo et al.Multiple sclerosis. 2005, Vol 11, Num 3, pp 367-371, issn 1352-4585, 5 p.Article

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesVACCA, Marcella; FILIPPINI, Francesco; CALZOLARI, Elisa et al.Journal of molecular medicine (Berlin. Print). 2001, Vol 78, Num 11, pp 648-655, issn 0946-2716Article