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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 3 4 5 6 Hits 21 – 40 of 106 21 Morphological influences on categorical perception of stop voicing in Welsh Anderson, Skye; Bell, Elise In: Proceedings of the Linguistic Society of America; Vol 3 (2018): Proceedings of the Linguistic Society of America; 14:–10 ; 2473-8689 (2018) BASE Show details 22 Une transformation sociale inévitable vers une identité commune et un partage de valeurs improbables ; An inevitable shift in society towards a common identity and improbably shared values Yuanfa, Zhu In: Hermès [ISSN 0767-9513], Les BRICS, un espace ignoré, 2017, 79, p. 157 (2017) BASE Show details 23 Gender and Mutation in Irish: a Preliminary Account for Further Investigation Frenda, Alessio S. In: The ITB Journal (2017) BASE Show details 24 Las mutaciones del gaélico irlandés ; The Irish Gaelic mutations Vázquez Diéguez, Ignacio In: Dialectologia: revista electrònica; 2017: Núm: 18; p. 157-180 (2017) BASE Show details 25 Testing-Based Conceptual Schema Validation in a Model-Driven Environment Granda Juca, María Fernanda. - : Universitat Politècnica de València, 2017 BASE Show details 26 Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability. ... Bathelt, Joe; Astle, Duncan; Barnes, Jessica; Raymond, Lucy; Baker, Kate. - : Apollo - University of Cambridge Repository, 2016 Abstract: Childhood speech and language deficits are highly prevalent and are a common feature of neurodevelopmental disorders. However, it is difficult to investigate the underlying causal pathways because many diagnostic groups have a heterogeneous aetiology. Studying disorders with a shared genetic cause and shared cognitive deficits can provide crucial insight into the cellular mechanisms and neural systems that give rise to those impairments. The current study investigated structural brain differences of individuals with mutations in ZDHHC9, which is associated with a specific neurodevelopmental phenotype including prominent speech and language impairments and intellectual disability. We used multiple structural neuroimaging methods to characterise neuroanatomy in this group, and observed bilateral reductions in cortical thickness in areas surrounding the temporo-parietal junction, parietal lobule, and inferior frontal lobe, and decreased microstructural integrity of cortical, subcortical-cortical, and ... Keyword: Acyltransferases; Adolescent; Adult; Brain; Epilepsy; Humans; Intellectual Disability; Language Development Disorders; Language Disorders; Loss of Function Mutation; Magnetic Resonance Imaging; Male; Neural Pathways; White Matter; Young Adult URL: https://www.repository.cam.ac.uk/handle/1810/276606 https://dx.doi.org/10.17863/cam.23906 BASE Hide details 27 Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability. Bathelt, Joe; Astle, Duncan; Barnes, Jessica. - : Elsevier BV, 2016. : Neuroimage Clin, 2016 BASE Show details 28 Seeing eye to eye Jean, Francesca. - : University of Alberta, 2016 BASE Show details 29 Seeing eye to eye Jean, Francesca. - 2016 BASE Show details 30 РЕЧЕВОЙ ЖАНР ЧАЙНОГО МЕНЮ: ВОПРОСЫ ДЕРИВАТОЛОГИИ ЗАВЯЗКИНА ИРИНА НИКОЛАЕВНА. - : Общество с ограниченной ответственностью Издательство Грамота, 2015 BASE Show details 31 РОЛЬ ОККАЗИОНАЛЬНЫХ НАИМЕНОВАНИЙ В ХУДОЖЕСТВЕННОМ ТЕКСТЕ (НА ПРИМЕРЕ ПОВЕСТИ В. С. ШЕФНЕРА «ДЕВУШКА У ОБРЫВА, ИЛИ ЗАПИСКИ КОВРИГИНА») КОЧКУРОВА НАТАЛЬЯ КОНСТАНТИНОВНА. - : Общество с ограниченной ответственностью Издательство Грамота, 2015 BASE Show details 32 Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations. Santarelli, Rosamaria; del Castillo, Ignacio; Cama, Elona... In: Hearing research, vol 330, iss Pt B (2015) BASE Show details 33 Questions of Reception and of Transmigration in Translation Raguet, Christine In: Conférence : Introducción a la Traductología ; https://halshs.archives-ouvertes.fr/halshs-01429525 ; Conférence : Introducción a la Traductología, ATRA, Universidad de Córdoba, Argentina, Jun 2015, Córdoba, Argentina (2015) BASE Show details 34 Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome Urbanowicz, Anna; Downs, Jenny; Girdler, Sonya... In: Research outputs 2014 to 2021 (2015) BASE Show details 35 A Refined Multiscale Self-Entropy Approach for the Assessment of Cardiac Control Complexity: Application to Long QT Syndrome Type 1 Patients Vlasta Bari; Giulia Girardengo; Andrea Marchi... In: Entropy ; Volume 17 ; Issue 11 ; Pages 7768-7785 (2015) BASE Show details 36 Mutation in Breton verbs: Pertinacity across generations Kennard, HJ; Lahiri, A In: Symplectic Elements at Oxford ; CrossRef ; ORA review team (2015) BASE Show details 37 Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population. Coussa, RG; Chakarova, C; Ajlan, R... In: Invest Ophthalmol Vis Sci , 56 (13) pp. 8297-8305. (2015) (2015) BASE Show details 38 Initial Consonant Mutation in Modern Irish: A Synchronic and Diachronic Analysis Robinson, Janine Fay In: Master's Theses (2015) BASE Show details 39 Linguistic changes in verbal expression: A preclinical marker of Alzheimer's disease Cuetos Vega, Fernando; Arango Lasprilla, Juan Carlos; Uribe, Claramonika. - 2015 BASE Show details 40 Paramutation phenomena in plants R. Pilu. - : Academic Press, 2015 BASE Show details Page: 1 2 3 4 5 6

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