Convergent neural signatures of speech prediction error are a biological marker for spoken word recognition. [PDF]
Nat CommunSohoglu E, Beckers L, Davis MH.
europepmc +1 more source
Commentary: Working Memory Load Affects Processing Time in Spoken Word Recognition: Test Retest Reliability of the E-WINDMIL Eyetracking Paradigm. [PDF]
Front Neurosci, 2021 Baharav S, Nitsan G, Ben-David BM.
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The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley +1 more source
COSMO-Onset: A Neurally-Inspired Computational Model of Spoken Word Recognition, Combining Top-Down Prediction and Bottom-Up Detection of Syllabic Onsets. [PDF]
Front Syst Neurosci, 2021 Nabé M, Schwartz JL, Diard J.
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Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle +26 more
wiley +1 more source
The role of inhibitory control in spoken word recognition: Evidence from cochlear implant users. [PDF]
Lang Cogn NeurosciColby SE, Smith FX, McMurray B.
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes +3 more
wiley +1 more source
Grammatical gender in spoken word recognition in school-age Spanish monolingual and Spanish-English bilingual children. [PDF]
Front PsycholBaron A +4 more
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline +3 more
wiley +1 more source