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Results 1 to 25 of 85

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MIRKO. IL BRONZO COME MAGIAMERCURI E.1975, 66 p.Book

EMILIO NOTTE. IMPEGNO POLITICO E AUTONOMIA POETICAMERCURI E.1974, 86 p.Book

ALESSANDRO VOLPIMERCURI E.1971, 191 p.Book

CAGLI. DALLA PITTURA ALL'ARAZZOMERCURI E.1973, 30 p.Book

Condições para o estudo, segundo depoimentos de alunos e professores de cursos de graduação = Study conditions according to information of college students and teachers = Enquête sur les conditions d'études auprès des étudiants et des enseignantsMERCURI, E.Pro-posições. 1994, Vol 5, Num 1, pp 61-71, issn 0103-7307Article

Marmora di CarraraMERCURI, E; RENE HOCKE, G.1980, 37 p.Book

Muscle histology vs MRI in Duchenne muscular dystrophyKINALI, M; ARECHAVALA-GOMEZA, V; QUINLIVAN, R. M et al.Neurology. 2011, Vol 76, Num 4, pp 346-353, issn 0028-3878, 8 p.Article

Expanding the clinical spectrum of POMT1 phenotypeD'AMICO, A; TESSA, A; MERCURI, E et al.Neurology. 2006, Vol 66, Num 10, issn 0028-3878, 1461,1564-1567 [5 p.]Article

Assessment of visual function in children with methylmalonic aciduria and homocystinuriaRICCI, D; PANE, M; DEODATO, F et al.Neuropediatrics. 2005, Vol 36, Num 3, pp 181-185, issn 0174-304X, 5 p.Article

Bone mineral density in a paediatric spinal muscular atrophy populationKINALI, M; BANKS, L. M; MERCURI, E et al.Neuropediatrics. 2004, Vol 35, Num 6, pp 325-328, issn 0174-304X, 4 p.Article

Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2)MERCURI, E; MANZUR, A. Y; JUNGBLUTH, H et al.Neurology. 2000, Vol 54, Num 8, pp 1704-1705, issn 0028-3878Article

Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI : A novel entity?MERCURI, E; SEWRY, Caroline A; BROWN, Susan C et al.Neuropediatrics. 2000, Vol 31, Num 4, pp 186-189, issn 0174-304XArticle

Correlation between visual function, neurodevelopmental outcome, and magnetic resonance imaging findings in infants with periventricular leucomalaciaCIONI, G; BERTUCCELLI, B; BOLDRINI, A et al.Archives of disease in childhood. Fetal and neonatal edition. 2000, Vol 82, Num 2, pp F134-F140, issn 1359-2998Article

Head growth in infants with hypoxic-ischemic encephalopathy: Correlation with neonatal magnetic resonance imagingMERCURI, E; RICCI, D; COWAN, F. M et al.Pediatrics (Evanston). 2000, Vol 106, Num 2, pp 235-243, issn 0031-4005, 1Article

Evaluation of the corpus callosum in clumsy children born prematurely : A functional and morphological studyMERCURI, E; JONGMANS, M; HENDERSON, S et al.Neuropediatrics. 1996, Vol 27, Num 6, pp 317-322, issn 0174-304XArticle

Autosomal recessive congenital cerebellar atrophy : a clinical and neuropsychological studyGUZZETTA, F; MERCURI, E; BONANNO, S et al.Brain & development (Tokyo. 1979). 1993, Vol 15, Num 6, pp 439-445, issn 0387-7604Article

Detection of common and private mutations in the COL6A1 gene of patients with bethlem myopathyLUCIOLI, S; GIUSTI, B; BÖNNEMANN, C et al.Neurology. 2005, Vol 64, Num 11, pp 1931-1937, issn 0028-3878, 7 p.Article

General movements detect early signs of hemiplegia in term infants with neonatal cerebral infarctionGUZZETTA, A; MERCURI, E; DUBOWITZ, L et al.Neuropediatrics. 2003, Vol 34, Num 2, pp 61-66, issn 0174-304X, 6 p.Article

Occipito-temporal polymicrogyria and subclinical muscular dystrophyZOLKIPLI, Z; HARTLEY, L; BROWN, S et al.Neuropediatrics. 2003, Vol 34, Num 2, pp 92-95, issn 0174-304X, 4 p.Article

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresJUNGBLUTH, H; MÜLLER, C. R; LAING, N. G et al.Neurology. 2002, Vol 59, Num 2, pp 284-287, issn 0028-3878Article

Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophyMERCURI, E; COUNSELL, S; ALLSOP, J et al.Neuropediatrics. 2002, Vol 33, Num 1, pp 10-14, issn 0174-304XArticle

Periodic lateralized epileptiform discharges (PLEDs) as early indicator of stroke in full-term newbornsRANDO, T; RICCI, D; MERCURI, E et al.Neuropediatrics. 2000, Vol 31, Num 4, pp 202-205, issn 0174-304XArticle

Occipital sawtooth : a physiological EEG pattern in very premature infantsBIAGIONI, E; FRISONE, M. F; LAROCHE, S et al.Clinical neurophysiology. 2000, Vol 111, Num 12, pp 2145-2149, issn 1388-2457Article

Cardiomyopathy in Duchenne, Becker, and sarcoglycanopathies : A role for coronary dysfunction ?GNECCHI-RUSCONE, T; TAYLOR, J; MERCURI, E et al.Muscle & nerve. 1999, Vol 22, Num 11, pp 1549-1556, issn 0148-639XArticle

Orientation-reversal and phase-reversal visual evoked potentials in full-term infants with brain lesions : A longitudinal studyMERCURI, E; BRADDICK, O; ATKINSON, J et al.Neuropediatrics. 1998, Vol 29, Num 4, pp 169-174, issn 0174-304XArticle

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