Search Results - (Author, Cooperation:G. Amabile)
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1A. Di Ruscio ; A. K. Ebralidze ; T. Benoukraf ; G. Amabile ; L. A. Goff ; J. Terragni ; M. E. Figueroa ; L. L. De Figueiredo Pontes ; M. Alberich-Jorda ; P. Zhang ; M. Wu ; F. D'Alo ; A. Melnick ; G. Leone ; K. K. Ebralidze ; S. Pradhan ; J. L. Rinn ; D. G. Tenen
Nature Publishing Group (NPG)
Published 2013Staff ViewPublication Date: 2013-10-11Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Base Sequence ; CCAAT-Enhancer-Binding Proteins/*genetics ; Cell Line ; DNA/genetics/metabolism ; DNA (Cytosine-5-)-Methyltransferase/*metabolism ; DNA Methylation/*genetics ; Gene Expression Profiling ; Gene Expression Regulation/*genetics ; Genome, Human/genetics ; Humans ; RNA, Messenger/genetics/metabolism ; RNA, Untranslated/genetics/*metabolism ; RNA-Binding Proteins/metabolism ; Substrate Specificity ; Transcription, Genetic/geneticsPublished by: -
2TRH-induced Growth Hormone and Brain-evoked Potential Changes in Humans An Experimental ContributionSTROLLO, F. ; AMABILE, G. ; STROLLO, G. ; FATTAPPOSTA, F. ; MORE, M. ; RIONDINO, G.
Oxford, UK : Blackwell Publishing Ltd
Published 1989Staff ViewISSN: 1749-6632Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: Natural Sciences in GeneralType of Medium: Electronic ResourceURL: -
3Fattapposta, F. ; Amabile, G. ; Chiarenza, G. ; Cordischi, M.V. ; D'Alessio, C. ; Di Venanzio, D. ; Foti, A. ; Pierelli, F. ; Morocutti, C.
Amsterdam : ElsevierStaff ViewISSN: 0167-8760Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: MedicinePsychologyType of Medium: Electronic ResourceURL: -
4Santorelli, F. M. ; De Joanna, G. ; Casali, C. ; Tessa, A. ; Siciliano, G. ; Amabile, G. A. ; Pierelli, F. ; Vilarinho, L. ; Santoro, L.
Springer
Published 2000Staff ViewISSN: 1573-2665Source: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract We studied six Italian patients harbouring multiple mitochondrial DNA (mtDNA) deletions in order to correlate clinical and molecular features. Earlier age at onset (17 vs 36 years), fewer ragged-red fibres (none vs 35%), and lower proportions of deleted mtDNAs (9 vs 33%) were found in one patient with autosomal recessive inheritance as compared to five with dominant transmission. Our findings add to the features associated with multiple deletions of mtDNA.Type of Medium: Electronic ResourceURL: -
5Staff View
ISSN: 1590-3478Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
6Staff View
ISSN: 1590-3478Keywords: Facial hemiatrophy ; scleroderma ; masseter spasmSource: Springer Online Journal Archives 1860-2000Topics: MedicineDescription / Table of Contents: Sommario In una donna di 39 anni è stata osservata la rara associazione di emiatrofia facciale progressiva, sclerodermia lineare e spasmo del muscolo massetere omolaterale. Sulla base dello studio elettrofisiologico nonché dalla revisione della letteratura, gli Autori discutono sul possibile significanto di tale associazione da un punto di vista patogenetico.Notes: Abstract The rare combination of progressive facial hemiatrophy, linear scleroderma and spasm of the homolateral masseter muscle was observed in a 39 year old woman. The possible pathogenetic meaning of the association is discussed on the electrophysiological evidence and in the light of published cases.Type of Medium: Electronic ResourceURL: -
7Staff View
ISSN: 1590-3478Keywords: “Top of the basilar” syndrome ; megadolichobasilar artery (MDBA) ; MRI, hemodynamic pathogenetic hypothesisSource: Springer Online Journal Archives 1860-2000Topics: MedicineDescription / Table of Contents: Sommario Viene descritto il caso di un paziente, con una storia di nevralgia trigeminale, che ha improvvisamente presentato una “top of the basilar syndrome”. La RMN rilevava lesioni ischemiche a livello del tetto del mesencefalo in sede paramediana sinistra, nel talamo ventrale sinistro, nel lobo occipitale sinistro e la presenza di una megadolicobasilare. L'associazione di una megadolicobasilare con una “top of the basilar syndrome” è rara in letteratura. Gli autori discutono il possibile meccanismo emodinamico che può aver prodotto la sindrome in presenza di una anomala megadolicobasilare.Notes: Abstract We describe the case of a patient with a history of trigeminal neuralgia who suddenly developed the “top of the basilar” syndrome. MRI disclosed ischemic lesions in the left paramedian mesencephalic tectum, in the left ventral thalamus, in the left occipital lobe and a megadolichobasilar artery (MDBA). The association of MDBA with the top of the basilar syndrome is rarely reported. We discuss the possible hemodynamic mechanism producing a top of the basilar syndrome in the presence of MDBA.Type of Medium: Electronic ResourceURL: