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L'ATROFIA OTTICA EREDITARIA DI LEBER. CONSIDERAZIONI ETIOPATOGENETICHE E LIMITI DIAGNOSTICI. = L'ATROPHIE OPTIQUE HEREDITAIRE DE LEBER. CONSIDERATIONS ETIOPATHOGENIQUES ET LIMITES DIAGNOSTIQUESLODATO G; ANASTASI M.1976; BELL. OCULIST.; ITAL.; DA. 1976; VOL. 55; NO 3-4; PP. 99-107; BIBL. 21 REF.Article

ASPETTI FLUORO-ANGIOGRAFICI ED ELETTROFUNZIONALI NELLA "COMMOTIO RETINAE" DI BERLIN = ASPECTS FLUOROANGIOGRAPHIQUES ET ELECTROFONCTIONNELS DANS LA "COMMOTION RETINIENNE" DE BERLINLODATO G; LAURICELLA M; ANASTASI M et al.1980; BOLL. OCUL.; ISSN 0006-677X; ITA; DA. 1980; VOL. 59; NO 5-6; PP. 357-365; ABS. ENG; BIBL. 16 REF.Article

IN TEMA DI NEOPLASIE DISONTOGENETICHE DEL TRATTO GENITALE FEMINILE. DIFFERENZE FORMALI ED ONTOISTOGENETICHE TRA TUMORE MISTO MESODERMALE, TUMORE MULLERIANO E SARCOMA STROMATICO DELL'UTERO = AU SUJET DES CANCERS DYSONTOGENETIQUES DES VOIES GENITALES FEMININES. DIFFERENCES MORPHOLOGIQUES ET ONTOHISTOGENETIQUES ENTRE TUMEUR MIXTE DU MESODERME, TUMEUR MUELLERIENNE ET SARCOME DU STROMA DE L'UTERUSTOMASINO RM; PERINO A; ANASTASI M et al.1974; ARCH. DE VECCHI ANAT. PATOL. MED. CLIN.; ITAL.; DA. 1974; VOL. 59; NO 2; PP. 293-318; BIBL. 1P.Article

POTENZIALI VISIVIN EVOCATI IN STATO DI ECCITAZIONE COSTANTE NELLA SCLEROSI MULTIPLA = POTENTIELS VISUELS EVOQUES EN EXCITATION CONSTANTE DANS LA SCLEROSE EN PLAQUESANASTASI M; GIORDANO G; LAURICELLA MR et al.1981; BOL. OCUL.; ISSN 0006-677X; ITA; DA. 1981; VOL. 60; NO 7-8; PP. 673-680; ABS. ENG; BIBL. 6 REF.Article

Electrofunctional features of the tilted disc syndromeGIUFFRE, G; ANASTASI, M.Documenta ophthalmologica. 1986, Vol 62, Num 3, pp 223-230, issn 0012-4486Article

Influence of crystalline lens on VEP latency in elderly patientsPONTE, F; ANASTASI, M; GIUFFRE, G et al.Documenta ophthalmologica. 1989, Vol 71, Num 4, pp 421-426, issn 0012-4486Article

Télangiectasies rétiniennes périphériques dans la rétinopathie pigmentaire = Peripheral retinal telangiectasis in retinitis pigmentosaLODATO, G; GIUFFRE, G; ANASTASI, M et al.Journal français d'ophtalmologie. 1987, Vol 10, Num 12, pp 777-782, issn 0181-5512Article

Clinical patterns and electrophysiological findings in retinal pigment epithelium diseases: does a correlation exist?PONTE, F; ANASTASI, M; CILLINO, S et al.Documenta ophthalmologica. 1986, Vol 62, Num 1, pp 73-79, issn 0012-4486Article

Surgical therapy for obesity can induce a vitamin A deficiency syndromeANASTASI, M; LAURICELLA, M; PONTE, F et al.Documenta ophthalmologica. 1995, Vol 90, Num 2, pp 143-155, issn 0012-4486Article

Methodological aspects of the application of the Naka-Rushton equation to clinical electroretinogramANASTASI, M; BRAI, M; LAURICELLA, M et al.Ophthalmic research. 1993, Vol 25, Num 3, pp 145-156, issn 0030-3747Article

Incomplete Wolfram syndrome: clinical and electrophysiologic study of two familial casesCILLINO, S; ANASTASI, M; LODATO, G et al.Graefe's archive for clinical and experimental ophthalmology. 1989, Vol 227, Num 2, pp 131-135, issn 0721-832XArticle

VECPs and optic disc damage in diabetesANASTASI, M; LODATO, G; CILLINO, S et al.Documenta ophthalmologica. 1987, Vol 66, Num 4, pp 331-336, issn 0012-4486Article

Retinitis pigmentosa and inner retina. Functional study by means of oscillatory potentials of the electroretinogramPONTE, F; ANASTASI, M; LAURICELLA, M. R et al.Documenta ophthalmologica. 1989, Vol 73, Num 4, pp 337-346, issn 0012-4486, 10 p.Article

Congenital insensitivity to pain with anhidrosis (NTRK1 mutation) and early onset renal disease : Clinical report on three sibs with a 25-year follow-up in one of themBARONE, R; LEMPEREUR, L; ANASTASI, M et al.Neuropediatrics. 2005, Vol 36, Num 4, pp 270-273, issn 0174-304X, 4 p.Article

A software framework for the generation of dynamic vulnerability maps for risk assessmentARENA, P; PATANE, L; CARUSO, S et al.Transactions on the built environment. 2009, Vol v. 110, pp 369-379, issn 1746-4498, isbn 978-1-8456-4202-0 1-8456-4202-3, 1Vol, 11 p.Conference Paper

An integrated system for disaster management in industrial areasARENA, P; PATANE, L; CARUSO, S et al.Transactions on the built environment. 2009, Vol v. 110, pp 381-390, issn 1746-4498, isbn 978-1-8456-4202-0 1-8456-4202-3, 1Vol, 10 p.Conference Paper

Two brothers with a variant of hereditary sensory neuropathyPAVONE, L; HUTTENLOCHER, P; SICILIANO, L et al.Neuropediatrics. 1992, Vol 23, Num 2, pp 92-95, issn 0174-304XArticle

Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21KOHL, S; BAUMANN, B; WISSINGER, B et al.Human molecular genetics (Print). 2000, Vol 9, Num 14, pp 2107-2116, issn 0964-6906Article

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