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au.\*:("DI MARIA, E")

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An explanation of firms’ internationalisation modes, blending firm heterogeneity and spatial agglomeration : microevidence from ItalyCAINELLI, G; DI MARIA, E; GANAU, R et al.Environment & planning A (Print). 2014, Vol 46, Num 4, pp 943-962, issn 0308-518X, 20 p.Article

Native chromatin―DNA structure and cell cycle: differential scanning calorimetry and gel electrophoresisNICOLINI, C; VERGANI, L; DIASPRO, A et al.Thermochimica acta. 1989, Vol 152, Num 2, pp 307-327, issn 0040-6031, 21 p.Article

Is Hardikar syndrome distinct from Kabuki (Niikawa―Kuroki) syndrome?EJARQUE, I; ULIANA, V; FORZANO, F et al.Clinical genetics. 2011, Vol 80, Num 5, pp 493-496, issn 0009-9163, 4 p.Article

Congenital hypomyelination due to myelin protein zero Q215X mutationMANDICH, P; MANCARDI, G. L; SCHENONE, A et al.Annals of neurology. 1999, Vol 45, Num 5, pp 676-678, issn 0364-5134Article

A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectDI MARIA, E; GULLI, R; BELLONE, E et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 10, pp 1495-1498, issn 0022-3050, 4 p.Article

HIGH Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriersCERAVOLO, R; ANTONINI, A; VOLTERRANI, D et al.Neurology. 2005, Vol 65, Num 12, pp 1971-1973, issn 0028-3878, 3 p.Article

Family and molecular data for a fine analysis of age at onset in Huntington diseaseSQUITIERI, F; SABBADINI, G; NOVELLETTO, A et al.American journal of medical genetics. 2000, Vol 95, Num 4, pp 366-373, issn 0148-7299Article

mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunitSCHITO, A. M; PIZZUTI, A; DI MARIA, E et al.Neuroscience letters. 1997, Vol 239, Num 1, pp 49-53, issn 0304-3940Article

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