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1
Longitudinal speech rate in progressive AOS (Utianski et al., 2021) ...
Utianski, Rene L.; Martin, Peter R.; Hanley, Holly. - : ASHA journals, 2021
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Communication changes in progressive AOS & aphasia (Utianski et al., 2021) ...
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3
Communication changes in progressive AOS & aphasia (Utianski et al., 2021) ...
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4
Longitudinal speech rate in progressive AOS (Utianski et al., 2021) ...
Utianski, Rene L.; Martin, Peter R.; Hanley, Holly. - : ASHA journals, 2021
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5
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech
In: Nat Commun (2021)
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6
Longitudinal neuroimaging biomarkers differ across Alzheimer’s disease phenotypes
In: Brain (2020)
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7
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant
In: Mov Disord Clin Pract (2019)
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8
Clinical and Neuroimaging Characteristics of Clinically Unclassifiable Primary Progressive Aphasia
In: Brain Lang (2019)
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9
The influence of β-amyloid on [(18)F]AV-1451 in semantic variant of primary progressive aphasia
Whitwell, Jennifer L.; Martin, Peter R.; Duffy, Joseph R.. - : Lippincott Williams & Wilkins, 2019
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10
Patterns of Neuropsychological Dysfunction and Cortical Volume Changes in Logopenic Aphasia
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11
[18F]AV-1451 tau-PET and primary progressive aphasia
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12
Tracing the Origins of Success: Implications for Successful Aging
Peterson, Nora M.; Martin, Peter. - : Oxford University Press, 2015
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13
Tracing the Origins of Success: Implications for Successful Aging
In: French Language and Literature Papers (2014)
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14
Bilingual competence and students' achievement in physics and mathematics
In: International journal of bilingual education and bilingualism. - Abingdon : Routledge, Taylor & Francis Group 14 (2011) 3, 335-345
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15
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
In: ISSN: 0022-2593 ; EISSN: 1468-6244 ; Journal of Medical Genetics ; https://hal.archives-ouvertes.fr/hal-00616882 ; Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (6), pp.396. ⟨10.1136/jmg.2010.087528⟩ (2011)
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16
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Kortüm, Fanny; Das, Soma; Flindt, Max. - : British Medical Journal Publishing Group, 2011
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17
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Kortüm, Fanny; Das, Soma; Flindt, Max. - : British Medical Journal Publishing Group, 2011
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18
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
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19
Separate and flexible bilingualism in complementary schools: Multiple language practices in interrelationship
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20
Imagining higher education as a multilingual space : guest editorial
In: Language and education. - Abingdon : Routledge, Taylor & Francis Group 24 (2010) 1, 3-8
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