DI IORIO, Giuseppe

DI IORIO, Giuseppe  

Dipartimento di Scienze Mediche e Chirurgiche Avanzate (DAMSS)  

Risultati 1 - 20 di 257 (tempo di esecuzione: 0.027 secondi).
Titolo Data di pubblicazione Autore(i) File
19. Fitc-conjugated plant agglutinins as specific saccharide stains for fluorescence microscopy of normal and pathologic muscles: preliminary results 1-gen-1980 DI IORIO, Giuseppe; R., Cotrufo; S., Pisanelli
39. Density and distribution of ConA and WGA receptors determined by histofluorescence analysis during degeneration, regeneration and reinnervation of the rat skeletal muscle following ischemia and reversible or irreversible denervation. , : , 1-gen-1986 DI IORIO, Giuseppe; R., Cotrufo; Lus, Giacomo; F., Grimaldi; C., Cutillo
7. (2011). Exome sequencing approach to define the complex genetic substrate in a family with insulin resistance, left ventricular noncompaction (LVNC) and congenital fiber type disproportion (CFTD). In: XLII Congress of the Italian Neurological Society. NEUROLOGICAL SCIENCES, p. S285, ISSN: 1590-1874, Torino, 22-25 novembre, 2011 1-gen-2011 Esposito, T; Formicola, D; Magliocca, S; Gianfrancesco, F; Simonetti, M; Farina, O; Cipullo, F; Samapolo, S; DI IORIO, Giuseppe
A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone 1-gen-1992 DI IORIO, Giuseppe; Picillo, U; Santanelli, P; Migliaresi, S; Bonavita, V.
A coding variant in GRIN3A gene is associated with migraine in italian population. 1-gen-2011 Formicola, D; Esposito, T; Magliocca, S; Gianfrancesco, F; Farina, O; Cipullo, F; Capone, E; Sampaolo, Simone; DI IORIO, Giuseppe
A comment on: 'Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy' by Paola Strocchi et al., FEBS Letters 359 (1995) 203-205 1-gen-1996 DI IORIO, Giuseppe; Sanges, G; Sampaolo, Simone; Bonavita, V.
A large kindred with autosomal dominant Parkinson's disease 1-gen-1990 Golbe, Li; DI IORIO, Giuseppe; Bonavita, V; Miller, Dc; Duvoisin, Rc
A large kindred with Paramyotonia Congenita 1-gen-1991 Sampaolo, Simone; DI IORIO, Giuseppe; G., Sanges; A., Cerracchio; M. L. A., Fratello; V., Sannino; B., Arnone; V., Bonavita
A large kindred with Parkinson's disease: onset age, segregation ratios and anticipation 1-gen-1992 L. I., Golbe; DI IORIO, Giuseppe; V., Bonavita; R. C., Duvoisin
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 1-gen-2000 DI IORIO, Giuseppe; Cappa, V; Ciccodicola, A; Sampaolo, Simone; Ammendola, A; Sanges, G; Giugliano, R; D'Urso, M.
A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1) 1-gen-2014 Melone, Mariarosa Anna Beatrice; Esposito, T; Uccello, R; Saracino, D; Capaldo, G; Dato, C; Allocca, S; DI IORIO, Giuseppe; Varriale, Bruno
A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease. A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease 1-gen-2014 Sampaolo, Simone; Esposito, T; Gianfrancesco, F; Napolitano, F; Lombardi, L; Lucà, R; Roperto, F; DI IORIO, Giuseppe
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 1-gen-2002 Mazzei, R; Conforti, Fl; Magariello, A; Bravaccio, C; Militerni, R; Gabriele, Al; Sampaolo, Simone; Patitucci, A; DI IORIO, Giuseppe; Muglia, M; Quattrone, A.
A promoter deletion at the dystrophin gene in a severe muscular Duchenne-like phenotype 1-gen-1997 Sampaolo, Simone; L., Pastore; V., Cappa; G., Frisso; R. M., Calise; F., Salvatore; DI IORIO, Giuseppe
A proposito di un nuovo caso di neuropatia ipertrofica familiare a trasmissione dominante, ad esordio precoce e ad evoluzione benigna 1-gen-1984 Bravaccio, F.; Ammendola, A.; DI IORIO, Giuseppe; Cotrufo, R.
A prospective study of cognitive function in Systemic Lupus Erythematosus 1-gen-1996 S., Migliaresi; S., Carlomagno; DI IORIO, Giuseppe; L., Ambrosone; M., Sannino; G., Sanges; U., Picillo; G., Tirri
A review of anatomy, pathology and clinical data on the nigrostriatal system 1-gen-1989 V., Bonavita; DI IORIO, Giuseppe
A somatic-nervous syndrome related to Marinesco-Sjogren's disease with some manifestations of Strumpell Lorrain's disease. Clinical report on five siblings 1-gen-1979 Guazzi, Gc; Amati, A; DEL VECCHIO, M; DI IORIO, Giuseppe; Fusco, G.
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients 1-gen-2002 Melone, Mariarosa Anna Beatrice; DI FEDE, G; Peluso, G; Lus, Giacomo; DI IORIO, Giuseppe; Sampaolo, Simone; Capasso, A; Gentile, Vittorio; Cotrufo, R.
Adult polyglucosan body disease; novel homozygous missense mutation in the glycogen-branching enzyme gene in an italian patient. 1-gen-2012 Farina, O; Cipullo, F; Simonetti, M; Formicola, D; Tortora, Fabio; Esposito, T; Sampaolo, Simone; DI IORIO, Giuseppe