Results 161 to 170 of about 69,676 (256)

Multidimensional Measurements of Dysarthria in Myotonic Dystrophy Type 1

International Journal of Language &Communication Disorders, Volume 61, Issue 3, May/June 2026.
ABSTRACT Background Myotonic dystrophy type 1 (DM1) is a heterogeneous neuromuscular disorder characterized by progressive muscle weakness and myotonia. Dysarthria is a known symptom of DM1, but literature is lacking about the patient's own perception in relationship to dysarthria characteristics and severity.
Sanne van Hellemond, Nicole Voet, Rosemarie Kroon, Yelda Sahin, Ilse Karnebeek, Marthè Nijkamp, Simone Knuijt   +6 more
wiley   +1 more source

Orthography [PDF]

, 2015
  +5 more sources

Parafoveal Processing of Orthographic, Phonological, and Semantic Information from Chinese Characters at a Distant Position: A Parafoveal Priming Study. [PDF]

Behav Sci (Basel)
Yuan X, Li S, Yan G.
europepmc   +1 more source

Narrative Ability in Swedish Children Treated for Posterior Fossa Tumours: Macro‐ and Microstructural Performance Before and 1–4 Weeks After Surgery

International Journal of Language &Communication Disorders, Volume 61, Issue 3, May/June 2026.
ABSTRACT Background Posterior fossa tumours (PFT), among the most common childhood brain tumours, place children at risk of speech, language, and communication difficulties, often described in relation to cerebellar mutism syndrome (CMS) but also seen in children without mutism.
K. Persson, D. Boeg Thomsen, K. Andersson, I. Tiberg, C. Castor, J. Grønbæk, R. Mathiasen, Å. Fyrberg   +7 more
wiley   +1 more source

Prevalence of Dyslexia and Its Relationship with Decoding and Comprehension in Persian-speaking Elementary Students. [PDF]

Indian J Psychol Med
Asadollahpour F, Mazaheri S, Shahouzaei N, Nakhaei MA.   +3 more
europepmc   +1 more source

The Genetic Origin of Uneven Cognitive Profiles in Heritable Neurodevelopmental Conditions and Individual Differences: Computational Investigations

Developmental Science, Volume 29, Issue 3, May 2026.
ABSTRACT While the heterogeneity and co‐occurrence of heritable neurodevelopmental conditions such as autism, attention deficit hyperactivity disorder (ADHD), and dyslexia remain issues of debate, these conditions are nevertheless all characterised by uneven cognitive profiles exhibiting strengths and weaknesses.
Maitrei Kohli, George Magoulas, Michael S. C. Thomas   +2 more
wiley   +1 more source

Comments on "Specific Learning Disability: Ten Challenges and Ten Recommendations in Current Indian Context". [PDF]

Indian J Psychol Med
Kannan PP, Kumar VM.
europepmc   +1 more source

Vowel Harmony in Lhasa Tibetan: Prosodic Analysis Applied to Interrelated Vocalic Features of Successive Syllables [PDF]

, 1961
Bell, Bloch, Carnochan, Dawchyuan, Gould, Gould, Hannah, R. K. Sprigg   +7 more
core   +1 more source

Exploring Acoustic Overlap in Second Language Vowel Productions

International Journal of Applied Linguistics, Volume 36, Issue 2, Page 1293-1304, May 2026.
ABSTRACT This study examines the alignment of vowel categories between second language (L2) learners and first language (L1) speakers of the target language, as well as potential overlaps between adjacent vowels in terms of formant frequencies and duration.
Georgios P. Georgiou, Elena Savva
wiley   +1 more source

Dissecting the Sublexical Route for Reading: Frontal and Parietal Networks Support Learned Orthography-to-Phonology Mappings. [PDF]

Neurobiol Lang (Camb)
Dyslin SM, DeMarco AT, Staples R, Dickens JV, Snider SF, Friedman R, Turkeltaub PE.   +6 more
europepmc   +1 more source