Results 281 to 290 of about 76,904 (360)

Language, Speech, and Oral Motor Performance in Children With Developmental Coordination Disorder: A Systematic Review

open access: yesInternational Journal of Language &Communication Disorders, Volume 60, Issue 5, September/October 2025.
Abstract Background Developmental coordination disorder is a neurodevelopmental disorder characterised by motor difficulties that significantly and persistently impact activities of daily living and participation. It has been suggested that children with (probable) developmental coordination disorder (pDCD) experience challenges in the domain of ...
Anna Fäldt   +2 more
wiley   +1 more source

Untargeted plasma metabolite detection in sudden sensorineural hearing loss: identifying key metabolic signatures. [PDF]

open access: yesFront Mol Biosci
Ma R   +10 more
europepmc   +1 more source

Consonant Proficiency in Children With and Without Hearing Impairment Assessed With Profiles of Early Expressive Phonological Skills – Swedish (PEEPS‐SE)

open access: yesInternational Journal of Language &Communication Disorders, Volume 60, Issue 5, September/October 2025.
ABSTRACT Background Children with hearing impairment (HI) are at risk for language difficulties, which can persist during childhood. There is a lack of clinical language tests adapted for young preschool children, enabling early identification of language delays. The expressive phonological test PEEPS‐SE could enable such testing in these ages.
Anna Persson   +4 more
wiley   +1 more source

Maternal Exposure to Medications and the Risk of Congenital and Early‐Onset Hearing Loss in Children: A Systematic Review and a Meta‐Analysis

open access: yesBasic &Clinical Pharmacology &Toxicology, Volume 137, Issue 3, September 2025.
ABSTRACT Background Congenital hearing loss (CHL) affects approximately 1–2 in 1000 children and significantly impacts development. Exposure to medications during pregnancy may impact offspring hearing; however, the ototoxic effects of different drugs have not been systematically investigated.
Asli Sena Kücükyildiz   +6 more
wiley   +1 more source

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

open access: yesClinical Genetics, Volume 108, Issue 3, Page 334-346, September 2025.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut   +7 more
wiley   +1 more source

The Usefulness of ETDQ‐7 Score in Assessing ETD

open access: yesClinical Otolaryngology, Volume 50, Issue 5, Page 840-847, September 2025.
ABSTRACT Introduction The ETDQ‐7 questionnaire has been validated for diagnosing Eustachian tube dysfunction (ETD) and a minimal clinically important difference (MCID) of > 3.5 has been suggested. We aim to assess the use of ETDQ‐7 for assessing ETD and a potential correlation between ETDQ‐7 and the Sino‐Nasal Outcome Test 22 (SNOT‐22). Methods ETD was
Niels Højvang Holm, Therese Ovesen
wiley   +1 more source

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