IRIS

DI IORIO, Giuseppe

DI IORIO, Giuseppe  

Dipartimento di Scienze Mediche e Chirurgiche Avanzate (DAMSS)  

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Risultati 1 - 20 di 259 (tempo di esecuzione: 0.044 secondi).
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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
[Aicardi's syndrome. Report of 2 cases] 1-gen-1978 Paolozzi, C; DI IORIO, Giuseppe; Petretta, V; Tata, Mr; Volpe, E; Guazzi, Gc
[Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family] 1-gen-1974 Guazzi, Gc; Stoppoloni, G; Ventruto, V; DI IORIO, Giuseppe
[Hunter's disease: genetic, clinical and biochemical study of a new family] 1-gen-1979 D'Auria, N; D'Amore, I; DI IORIO, Giuseppe; Annunziata, P; Puoti, S; Federico, A.
[Introduction to neuroimmunology] 1-gen-1989 Bonavita, V; DI IORIO, Giuseppe
[Neurological manifestations of systemic lupus erythematosus. Study of 53 cases] 1-gen-1989 Migliaresi, S; DI IORIO, Giuseppe; Picillo, U; Tedeschi, Gioacchino; Santanelli, P; DI COSTANZO, A; DELLA CIOPPA, G; Fasolino, M; Diano, A; Bonavita, V.
[Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case] 1-gen-1979 Cotrufo, R; DI IORIO, Giuseppe; Aguglia, U; Cotticelli, L; D'Auria, N; Bonavita, V.
[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia] 1-gen-2001 Migliaresi, S; DI IORIO, Giuseppe; Ammendola, A; Ambrosone, L; Sanges, G; Ugolini, G; Sampaolo, Simone; Bravaccio, F; Tirri, G.
[Unusual histo-cytopathologic findings in a familial case of stiff spine syndrome] 1-gen-1986 DI IORIO, Giuseppe; Lus, Giacomo; DE CRISTOFARO, M; Cutillo, C; Cecio, A; Corona, M; Guastafierro, Vf; Cotrufo, R.
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 case of Kohlmeier-Degos disease with dramatic neurological involvment 1-gen-2017 Saracino, D; D'Armiento, Fp; Napolitano, M; Ayala, F; Di Iorio, G; Puoti, G
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia? 1-gen-2015 Coppola, Cinzia; Saracino, D; Califano, F; Barbarulo, Anna maria; Di Fede, G; Piccoli, E; Tagliavini, F; DI IORIO, Giuseppe; Rossi, G. 3.
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 1-gen-2016 Saracino, D; Coppola, C; Puoti, G; Lus, G; Dato, C; le Ber, I; Caroppo, P; Piccoli, F; Tagliavini, F; Di Iorio, G; Rossi, G
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 1-gen-2017 Coppola, Cinzia; Saracino, Dario; Puoti, Gianfranco; Lus, Giacomo; Dato, Clemente; Le Ber, Isabelle; Pariente, Jeremie; Caroppo, Paola; Piccoli, Elena; Tagliavini, Fabrizio; DI IORIO, Giuseppe; Rossi, Giacomina
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