Zobrazeno 1 - 10
of 730
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
Autor:
Zappella, M.
Publikováno v:
Neuroscience & Behavioral Physiology; Jan2023, Vol. 53 Issue 1, p34-39, 6p
Autor:
J. M. Berg, M. Zappella
Publikováno v:
Journal of Intellectual Disability Research. 8:44-54
Autor:
M. Zappella
Publikováno v:
European Child & Adolescent Psychiatry. 11:18-23
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
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
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
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
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