M
Mauro Celli
Researcher at Sapienza University of Rome
Publications - 53
Citations - 1003
Mauro Celli is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Osteogenesis imperfecta & Medicine. The author has an hindex of 14, co-authored 49 publications receiving 891 citations. Previous affiliations of Mauro Celli include Policlinico Umberto I.
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Journal ArticleDOI
Abnormal intestinal permeability in children with autism.
Patrizia D'Eufemia,Mauro Celli,R. Finocchiaro,Lucia Pacifico,L Viozzi,M. Zaccagnini,Ettore Cardi,Omero Giardini +7 more
TL;DR: It is speculated that an altered intestinal permeability could represent a possible mechanism for the increased passage through the gut mucosa of peptides derived from foods with subsequent behavioural abnormalities.
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Low serum tryptophan to large neutral amino acids ratio in idiopathic infantile autism
TL;DR: A low brain tryptophan availability due to a low serum Try/LNAA ratio could be one of the possible mechanisms involved in the alteration of serotonergic function in autism.
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Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.
Margherita Maioli,Maria Gnoli,Manila Boarini,Morena Tremosini,Anna Zambrano,Elena Pedrini,Marina Mordenti,Serena Corsini,Patrizia D'Eufemia,Paolo Versacci,Mauro Celli,Luca Sangiorgi +11 more
TL;DR: Despite difficulties still present in defining clear rules to predict the clinical outcome in OI patients, this study provides new pieces for completing the puzzle, thanks to the inclusion of clinical signs never considered before and to the large number of OI Italian patients.
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Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype
Freya Swinnen,Paul Coucke,Anne De Paepe,Sofie Symoens,Fransiska Malfait,Filomena Valentina Gentile,Luca Sangiorgi,Patrizia D'Eufemia,Mauro Celli,Ton J. T. M. Garretsen,Cor W. R. J. Cremers,Ingeborg Dhooge,Els De Leenheer +12 more
TL;DR: The hearing impairment usually starts between the second and fourth decade of life as a conductive hearing loss, frequently evolving to mixed hearing loss thereafter, and a minority of patients develop pure sensorineural hearing loss as discussed by the authors.
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Child with manifestations of dermotrichic syndrome and ichthyosis follicularis‐alopecia‐photophobia (IFAP) syndrome
F. Martino,P. D'Eufemia,M. S. Pergola,R. Finocchiaro,Mauro Celli,G. Giampà,M. Frontali,O. Giardini +7 more
TL;DR: The clinical findings include all the features that dermotrichic and ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome have in common and in addition those that characterize IFAP syndrome (photophobia, recurrent respiratory infections, etc).