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Inhibition of neuroblastoma cell growth by TREX1-mutated human lymphocytesPULLIERO, A; MARENGO, B; DOMENICOTTI, C et al.Oncology reports. 2012, Vol 27, Num 5, pp 1689-1694, issn 1021-335X, 6 p.Article

Aicardi-Goutières syndromeORCESI, S; LA PIANA, R; FAZZI, E et al.British medical bulletin. 2009, Vol 89, pp 183-201, issn 0007-1420, 19 p.Article

Aicardi-Goutières Syndrome: Neuroradiologic Findings and Follow-UpUGGETTI, C; LA PIANA, R; ORCESI, S et al.American journal of neuroradiology. 2009, Vol 30, Num 10, pp 1971-1976, issn 0195-6108, 6 p.Article

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyMERCURI, E; BERTINI, E; CINI, C et al.Neurology. 2007, Vol 68, Num 1, pp 51-55, issn 0028-3878, 5 p.Article

Body composition and energy expenditure in Duchenne muscular dystrophyZANARDI, M. C; TAGLIABUE, A; ORCESI, S et al.European journal of clinical nutrition. 2003, Vol 57, Num 2, pp 273-278, issn 0954-3007, 6 p.Article

Effect of preterm premature rupture of membranes on neurodevelopmental outcome : follow up at two years of ageSPINILLO, A; CAPUZZO, E; STRONATI, M et al.British journal of obstetrics and gynaecology (Print). 1995, Vol 102, Num 11, pp 882-887, issn 0306-5456Article

Prevalence of tic disorders among primary school students in the city of Pavia, ItalyLANZI, G; ZAMBRINO, C. A; TERMINE, C et al.Archives of disease in childhood. 2004, Vol 89, Num 1, pp 45-47, issn 0003-9888, 3 p.Article

A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophyBONIFATI, M. D; RUZZA, G; BONOMETTO, P et al.Muscle & nerve. 2000, Vol 23, Num 9, pp 1344-1347, issn 0148-639XArticle

Cerebral cavernous angiomas : an atypical case in infancyLANZI, G; FAZZI, E; ORCESI, S et al.Child's nervous system (Print). 1997, Vol 13, Num 7, pp 412-414, issn 0256-7040Article

Perinatal factors and 2-year minor neurodevelopmental impairment in low birth weight infantsSPINILLO, A; FAZZI, E; ORCESI, S et al.Biology of the neonate. 1995, Vol 67, Num 1, pp 39-46, issn 0006-3126Article

Neurodevelopmental outcome in very-low-birth-weight infants with or without periventricular haemorrhage and/or leucomalaciaFAZZI, E; LANZI, G; GERARDO, A et al.Acta paediatrica (Oslo). 1992, Vol 81, Num 10, pp 808-811, issn 0803-5253Article

Le nouveau-né hypotoniqueORCESI, S; RAVELLI, C; FAZZI, E et al.Médecine & enfance. 2012, Vol 32, Num 9, pp 363-369, issn 0291-0233, 7 p.Article

New molecular findings in congenital myopathies due to selenoprotein N gene mutationsCAGLIANI, R; FRUGUGLIETTI, M. E; PICHIECCHIO, A et al.Journal of the neurological sciences. 2011, Vol 300, Num 1-2, pp 107-113, issn 0022-510X, 7 p.Article

COL4A1 Mutations Associated with a Characteristic Pattern of Intracranial CalcificationLIVINGSTON, J; DOHERTY, D; KNEEN, R et al.Neuropediatrics. 2011, Vol 42, Num 6, pp 227-233, issn 0174-304X, 7 p.Article

The natural history of Aicardi-Goutières syndrome : Follow-up of 11 Italian patientsLANZI, G; FAZZI, E; D'ARRIGO, S et al.Neurology. 2005, Vol 64, Num 9, pp 1621-1624, issn 0028-3878, 4 p.Article

Neurodevelopmental outcome at 5-7 years in preterm infants with periventricular LeukomalaciaFAZZI, E; ORCESI, S; CAFFI, L et al.Neuropediatrics. 1994, Vol 25, Num 3, pp 134-139, issn 0174-304XArticle

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