Zobrazeno 1 - 10
of 249
pro vyhledávání: '"M Zappella"'
Autor:
M. Zappella
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 122:71
In the last decades autism diagnosis has shown great differences in prevalence studies, apparently related to methods applied in the evaluation of children with relational and\or communicative difficulties. In the present study a literature evaluatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd57496b52ddd44934e4bb0f7c9f5a93
https://doi.org/10.17116/jnevro202212206171
https://doi.org/10.17116/jnevro202212206171
Akademický článek
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Autor:
J. M. Berg, M. Zappella
Publikováno v:
Journal of Intellectual Disability Research. 8:44-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ce1f2049b7024d6eb529dee706349e3
https://doi.org/10.1111/j.1365-2788.1964.tb00799.x
https://doi.org/10.1111/j.1365-2788.1964.tb00799.x
Autor:
Stefania Rossi, Luigi Gennari, S. Martini, Chiara Cepollaro, D. Bruni, S Pacini, S. Gonnelli, Carlo Gennari, M. Zappella, G. Hayek, M.B. Franci
Publikováno v:
Calcified Tissue International. 69:259-262
This study evaluated bone status and bone turnover in 82 females (ages 2-21 years) with the Rett Syndrome (RS) and 82 age-matched controls. Bone mineral density (BMD) by dual X-ray absorptiometry (DXA) at the ultradistal and proximal radius and ultra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::069525be8472ee4363547c466b7aa65a
https://doi.org/10.1007/s002230010027
https://doi.org/10.1007/s002230010027
Akademický článek
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Autor:
Youssef Hayek, Angelo Vattimo, P Bertelli, M Zappella, A. M. Aucone, Duccio Volterrani, Luca Burroni, Alessandra Vella
Publikováno v:
Europe PubMed Central
Rett syndrome is a progressive neurological paediatric disorder associated with severe mental deficiency, which affects only girls. The aim of this study was to determine if brain blood flow abnormalities detected with 99 Tc m -ethyl-cysteinate-dimer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b091c24ecd07ff31c2e38479362a289d
https://doi.org/10.1097/00006231-199706000-00005
https://doi.org/10.1097/00006231-199706000-00005
Akademický článek
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Publikováno v:
Annali dell'Istituto superiore di sanita. 37(4)
Rett syndrome (RS) is a progressive neurodevelopmental disorder predominant in females, characterised by mental deficiency, stereotyped hand-washing and apraxia. Notwithstanding the recent identification of the MECP2 gene likely involved in the patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b82f758e930ff8b9bd0c8bb525013fe3
https://pubmed.ncbi.nlm.nih.gov/12046231
https://pubmed.ncbi.nlm.nih.gov/12046231
Autor:
M, Zappella
Publikováno v:
European childadolescent psychiatry. 11(1)
Early-onset Tourette syndrome comorbid with reversible autistic behaviour is described in twelve young males. After a normal gestation, delivery and first-year development, regression set in between the age of one and two with loss of various abiliti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54f92d1998a7606837ede345fac3253f
https://pubmed.ncbi.nlm.nih.gov/12747386
https://pubmed.ncbi.nlm.nih.gov/12747386
Autor:
A, Philippe, M, Martinez, M, Guilloud-Bataille, C, Gillberg, M, Råstam, E, Sponheim, M, Coleman, M, Zappella, H, Aschauer, L, Van Maldergem, C, Penet, J, Feingold, A, Brice, M, Leboyer, L, van Malldergerme
Publikováno v:
Human molecular genetics. 8(5)
Family and twin studies have suggested a genetic component in autism. We performed a genome-wide screen with 264 microsatellites markers in 51 multiplex families, using non-parametric linkage methods. Families were recruited by a collaborative group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00b9fc62646aa8859255a03e4c4f5d37
https://pubmed.ncbi.nlm.nih.gov/10196369
https://pubmed.ncbi.nlm.nih.gov/10196369