Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Simona Trillo"'
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
The speech of individuals with schizophrenia exhibits atypical prosody and pragmatic dysfunctions, producing monotony. The paper presents the outcomes of corpus-based research on the prosodic features of the pathology as they manifest in real-life sp
Externí odkaz:
https://doaj.org/article/9192a192e5514c5d9ce181fe0778a278
Autor:
Maurizio Elia, Roberto Sacco, Monica Saccani, Alessandro Frolli, Antonio M. Persico, Cindy Schneider, Carmela Bravaccio, Karl L. Reichelt, Antonella Gritti, Paolo Curatolo, Roberto Militerni, Tiziana Pascucci, C. Lenti, Stefano Puglisi-Allegra, Raun Melmed, Barbara Manzi, Simona Trillo
Publikováno v:
Biological psychiatry. 62(9)
Head growth rates are often accelerated in autism. This study is aimed at defining the clinical, morphological, and biochemical correlates of head circumference in autistic patients.Fronto-occipital head circumference was measured in 241 nonsyndromic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a592475affff14686112699bc4383c
https://pubmed.ncbi.nlm.nih.gov/17644070
https://pubmed.ncbi.nlm.nih.gov/17644070
Autor:
Raun Melmed, Leonardo D'Agruma, Vito Guarnieri, Lucia Anna Muscarella, Maria Lucia Mascia, Simona Trillo, Roberto Sacco, Maurizio Elia, Emanuela Rucci, Antonio M. Persico, Cindy Schneider, Maria Rosaria Piemontese, Carmela Bravaccio, Roberto Militerni
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (3)
We previously described a significant association between the HOXA1 G218 allele and increased head circumference in autism [Conciatori et al. (2004); Biol Psychiatry 55:413–419]. The present study reveals identical effects also in normal children.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e7fb7984f014f57472726021910ae1
https://pubmed.ncbi.nlm.nih.gov/17171652
https://pubmed.ncbi.nlm.nih.gov/17171652
Autor:
James S. Sutcliffe, Pat Levitt, Cindy Schneider, Antonio M. Persico, Carmela Bravaccio, Simona Trillo, Daniel B. Campbell, Roberto Militerni, Maurizio Elia, Philip J. Ebert, Raun Melmed, Roberto Sacco
There is strong evidence for a genetic predisposition to autism and an intense interest in discovering heritable risk factors that disrupt gene function. Based on neurobiological findings and location within a chromosome 7q31 autism candidate gene re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811e942b4d746c676b7a931e7484a3e9
http://hdl.handle.net/11570/3121928
http://hdl.handle.net/11570/3121928
Autor:
Fabio Macciardi, Roberto Militerni, Carmela Bravaccio, Xudong Liu, Leonardo D'Agruma, Karl L. Reichelt, Roberto Sacco, I. Ricci, Simona Trillo, Cindy Schneider, Jeanette J. A. Holden, Tiziana Pascucci, Maurizio Elia, Raun Melmed, Marcello D'Amelio, Lucia Anna Muscarella, Vito Guarnieri, Antonio M. Persico, Stefano Puglisi-Allegra
Publikováno v:
Molecular psychiatry. 10(11)
Organophosphates (OPs) are routinely used as pesticides in agriculture and as insecticides within the household. Our prior work on Reelin and APOE delineated a gene–environment interactive model of autism pathogenesis, whereby genetically vulnerabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdc8e4c71817d5ac8361b5f8ca51ff4e
https://pubmed.ncbi.nlm.nih.gov/16027737
https://pubmed.ncbi.nlm.nih.gov/16027737
Autor:
Lucianna Muscarella, Karl L. Reichelt, Melanie O'Bara, Monica Conciatori, Cindy Schneider, Maurizio Elia, Lori Crawford, Roberto Militerni, Sarah J. Spence, Francesco Montecchi, Alessandro Quattrone, Antonio M. Persico, Vito Guarnieri, Stefano Puglisi-Allegra, Christopher J. Stodgell, Carmela Bravaccio, Leopoldo Zelante, Daniel Rabinowitz, Patricia M. Rodier, Susan L. Hyman, Raun Melmed, Tiziana Pascucci, Leonardo D'Agruma, Simona Trillo
The HOXA1 gene plays a major role in brainstem and cranial morphogenesis. The G allele of the HOXA1 A218G polymorphism has been previously found associated with autism.We performed case-control and family-based association analyses, contrasting 127 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::706b409e5fd35cf8bcd535f02f7a4082
http://hdl.handle.net/11570/3122074
http://hdl.handle.net/11570/3122074
Autor:
Maurizio Elia, Tiziana Pascucci, Vito Guarnieri, M. Palermo, Raun Melmed, Leopoldo Zelante, Cindy Schneider, J. M. Melgari, Leonardo D'Agruma, Monica Conciatori, Simona Trillo, Roberto Militerni, Carmela Bravaccio, Flavio Keller, Reichelt Karl L, Lucia Anna Muscarella, Antonio M. Persico, Stefano Puglisi-Allegra, Daniel Rabinowitz, Francesco Montecchi
We have previously described linkage/association between reelin gene polymorphisms and autistic disorder. APOE also participates in the Reelin signaling pathway, by competitively antagonizing Reelin binding to APOE receptor 2 and to very-low-density
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6eaee96f69b32af2d4f4c0816f8156c
http://hdl.handle.net/11573/234415
http://hdl.handle.net/11573/234415
Adenosine deaminase alleles and autistic disorder: Case-control and family-based association studies
Autor:
Tiziana Pascucci, Simona Trillo, Carmela Bravaccio, Roberto Militerni, M. Palermo, Francesco Montecchi, Karl L. Reichelt, Stefano Puglisi-Allegra, Antonio M. Persico, Monica Conciatori, Raun Melmed, Flavio Keller, Cindy Schneider, Alfonso Baldi
Publikováno v:
Scopus-Elsevier
Adenosine deaminase (ADA) plays a relevant role in purine metabolism, immune responses, and peptidase activity, which may be altered in some autistic patients. Codominant ADA1 and ADA2 alleles code for ADA1 and ADA2 allozymes, the most frequent prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f44ec4e98794774ff7bc8873a24264cc
http://hdl.handle.net/11591/229886
http://hdl.handle.net/11591/229886
Autor:
Tiziana Pascucci, Veruska Papaleo, Francis Rousseau, Jörg Hager, Karl L. Reichelt, Stefano Puglisi-Allegra, Rainald Moessner, Maurizio Elia, Antonio M. Persico, Paolo Curatolo, Cindy Schneider, Simona Trillo, Roberto Militerni, Carmela Bravaccio, Roberto Sacco, Barbara Manzi, Raun Melmed
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 8, Iss 1, p 11 (2007)
BMC Medical Genetics, Vol 8, Iss 1, p 11 (2007)
Background The TPH2 gene encodes the enzyme responsible for serotonin (5-HT) synthesis in the Central Nervous System (CNS). Stereotypic and repetitive behaviors are influenced by 5-HT, and initial studies report an association of TPH2 alleles with ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9988c2f33a0d4d71972ce6330a48f30