Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mental Retardation: complications"'
Autor:
Rowland P. Barrett
It is well known that behavior problems are a salient characteristic of children and adults with mental retardation. That is not to say that all persons with mental retardation experience behavior disorders; how ever, most studies indicate that the
Autor:
F.J. Menolascino, J.A. Stark
This volume aims to provide the reader with a contemporary account of his torical, diagnostic, treatment-management (including the individual and the service systems perspectives), and training dimensions of mentally ill/mentally retarded individua
Autor:
V. Scarano, Giuseppe De Michele, Paolo Gasparini, Lucio Santoro, Giovanni Coppola, Anna Perretti, Filippo M. Santorelli, Alessandro Filla, Sandro Banfi, Adamo Pio d'Adamo, Francesco Saccà, Chiara Criscuolo, Pasquale Striano, Anna E. Lehesjoki, Salvatore Striano, Vincenzo Brescia Morra, Fabrizio Barbieri
We describe two couples of sibs from a southern Italian family affected by epilepsy, myoclonus, mental retardation and slight ataxia. Onset was between 4 and 12 years and the course slowly progressive. The clinical picture suggested the diagnosis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3159fccb024d61cf37016b521b9df23
http://hdl.handle.net/11588/480236
http://hdl.handle.net/11588/480236
Autor:
M. Pat Malloy, Walter J. Muir, John A.L. Armour, Edward J. Hollox, Douglas Blackwood, Ben S. Pickard, David J. Porteous
Publikováno v:
BMC Medical Genetics, Vol 5, Iss 1, p 21 (2004)
Pickard, B S, Hollox, E J, Malloy, M P, Porteous, D J, Blackwood, D H, Armour, J A & Muir, W J 2004, ' A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation ', BMC Medical Genetics, vol. 5, pp. 21 . https://doi.org/10.1186/1471-2350-5-21
BMC Medical Genetics
Pickard, B S, Hollox, E J, Malloy, M P, Porteous, D J, Blackwood, D H, Armour, J A & Muir, W J 2004, ' A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation ', BMC Medical Genetics, vol. 5, pp. 21 . https://doi.org/10.1186/1471-2350-5-21
BMC Medical Genetics
Background Cryptic structural abnormalities within the subtelomeric regions of chromosomes have been the focus of much recent research because of their discovery in a percentage of people with mental retardation (UK terminology: learning disability).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8724ee95bbae053105f9c33278f591
http://www.biomedcentral.com/1471-2350/5/21
http://www.biomedcentral.com/1471-2350/5/21
Autor:
Dan, Bernard, Chéron, Guy
Publikováno v:
Revue neurologique, 159 (5 Pt 1
Angelman syndrome is a neurogenetic disorder characterized by developmental delay, absence of speech, motor impairment, epilepsy and a peculiar behavioural phenotype associated with abnormalities of chromosome 15q11-13. Precise diagnosis carries clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2101::e6b7c9532ce279a97480248d73fbf508
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53472
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53472
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