Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Grazia Giana"'
Publikováno v:
Open Journal of Psychiatry. :329-334
The present study describes the occurrence of psychiatric comorbid disorders in a cohort of 86 high functioning autism (HFA)/Asperger syndrome (AS) patients, examined at Child Neurology and Psychiatry Unit of Tor Vergata University. 38 patients out o
Publikováno v:
Journal of Child Neurology. 23:307-314
Autism is an etiologic heterogeneous entity caused by many different diseases occurring in the central nervous system at an early stage in life. Several metabolic defects have been associated with autistic symptoms with a rate higher than that found
Autor:
Luigi Tarani, Miriam Troianiello, Esterina Pascale, Domenica Travaglini, Walter Adriani, Giovanni Laviola, Maria Cristina Porfirio, Grazia Giana, Emilia Romano, Paolo Curatolo, Oleg Granstrem, Silvia Giovinazzo, Roberto D'Ambrosio, Eleonora Barlocci
Interest is rising for auto-immune contribution in neuro-psychiatry. We evaluated the auto-antibodies against dopamine transporter (DAT aAbs) in 61 children (46 ADHD who met DSM-IV-TR criteria, 15 healthy controls). Methods ADHD patients were assigne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1356fd72aefb0d1912a5614b02cb90c
http://hdl.handle.net/2108/116873
http://hdl.handle.net/2108/116873
Autor:
Renato Donfrancesco, Elda Andriola, Michela Di Trani, Grazia Giana, Silvia Miano, Maria Cristina Porfirio
Some clinical studies on attention deficit hyperactivity disorder (ADHD) have been found to overlap those of studies on personality, particularly those on the Novelty Seeking trait (NS) as measured by the Junior Temperament and Character Inventory (J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b828902d02e2ba474fae6fed14eeab1
http://hdl.handle.net/11573/934490
http://hdl.handle.net/11573/934490
Autor:
Grazia Giana, Samuele Cortese, Adriana Lo-Castro, Marie Christine Mouren, Paolo Curatolo, Silvia Giovinazzo, Diane Purper-Ouakil, Maria Cristina Porfirio
Publikováno v:
Medical Hypotheses
Medical Hypotheses, Elsevier, 2015, 84 (1), pp.4-7. ⟨10.1016/j.mehy.2014.11.004⟩
Medical Hypotheses, Elsevier, 2015, 84 (1), pp.4-7. ⟨10.1016/j.mehy.2014.11.004⟩
International audience; Besides the crucial role of genetic susceptibility in the development of early-onset obesity, it has been shown that feeding behavior could contribute to increased body weight. A significant association between obesity/overwei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85c1dd18c8d13c723b6d9ca2fbbda1b6
https://hal.archives-ouvertes.fr/hal-02164786
https://hal.archives-ouvertes.fr/hal-02164786
Autor:
Maria Cristina Porfirio, Grazia Giana, Paolo Curatolo, Cinzia Galasso, Diane Purper Ouakil, Adriana Lo-Castro, Silvia Giovinazzo
We report the case of a young male with attention-deficit hyperactivity disorder, oppositional defiant disorder, eating problems and overweight, and mild mental retardation. Karyotype analysis detected an apparently balanced translocation: t(1;2)(p34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb88037825549f41f1e6e5144d7d1b0f
http://hdl.handle.net/2108/77689
http://hdl.handle.net/2108/77689
Autor:
Carmela Bravaccio, Riccardo Alessandrelli, Roberto Sacco, Vito Guarnieri, Barbara Manzi, Cindy Schneider, Leonardo D'Agruma, Monica Saccani, Paolo Curatolo, Antonio M. Persico, Grazia Giana, Roberto Militerni, Raun Melmed, Lucia Anna Muscarella, C. Lenti
Publikováno v:
Molecular Autism, Vol 1, Iss 1, p 9 (2010)
Molecular Autism
Molecular Autism
Background HOXB1 plays a major role in brainstem morphogenesis and could partly determine the cranial circumference in conjunction with HOXA1. In our sample, HOXA1 alleles significantly influence head growth rates both in autistic patients and in pop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30e051af23134e8ff4412dfa2f844cb7
http://hdl.handle.net/2108/19072
http://hdl.handle.net/2108/19072
Autor:
Marco Fichera, Grazia Giana, Cinzia Galasso, Lucia Grillo, Sebastiano A. Musumeci, Lucia Castiglia, Paolo Curatolo, Adriana Lo-Castro
We describe a 7-year-old patient with autism, moderate mental retardation, secondary microcephaly, agenesis of right optic nerve, and dysmorphic features carrying a de novo cryptic deletion of chromosome 2p25.2, detected by aCGH. Pure monosomies of 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c039bf6c588179a005b280cc57c1954
http://hdl.handle.net/20.500.11769/29617
http://hdl.handle.net/20.500.11769/29617