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Showing results for eric hearing
Your search for Eric Heuring retrieved no results
Music education for improving reading skills in children and adolescents with dyslexia.
Cogo-Moreira H, Andriolo RB, Yazigi L, Ploubidis GB, Brandão de Ávila CR, Mari JJ. Cogo-Moreira H, et al. Cochrane Database Syst Rev. 2012 Aug 15;(8):CD009133. doi: 10.1002/14651858.CD009133.pub2. Cochrane Database Syst Rev. 2012. PMID: 22895983 Free article. Review.
It is marked by difficulties with accurate or fluent recognition of words and poor spelling in people who have average or above average intelligence and these difficulties cannot be attributed to another cause, for example, poor vision, hearing difficulty, or lack of socio …
It is marked by difficulties with accurate or fluent recognition of words and poor spelling in people who have average or above average inte …
Follow-up in newborn hearing screening - A systematic review.
Ravi R, Gunjawate DR, Yerraguntla K, Lewis LE, Driscoll C, Rajashekhar B. Ravi R, et al. Int J Pediatr Otorhinolaryngol. 2016 Nov;90:29-36. doi: 10.1016/j.ijporl.2016.08.016. Epub 2016 Aug 26. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27729148 Review.
INTRODUCTION: The quality and efficiency of newborn hearing screening programs (NHS) rely heavily on appropriate follow-up. The Joint Committee on Infant Hearing recommends a follow-up rate of more than 95% of infants who fail the initial hearing screening. . …
INTRODUCTION: The quality and efficiency of newborn hearing screening programs (NHS) rely heavily on appropriate follow-up. The Joint …
Non-speech oral motor treatment for children with developmental speech sound disorders.
Lee AS, Gibbon FE. Lee AS, et al. Cochrane Database Syst Rev. 2015 Mar 25;2015(3):CD009383. doi: 10.1002/14651858.CD009383.pub2. Cochrane Database Syst Rev. 2015. PMID: 25805060 Free PMC article. Review.
These speech difficulties could be due to structural, sensory or neurophysiological causes (e.g. hearing impairment), but more often the cause of the problem is unknown. ...SEARCH METHODS: In April 2014 we searched the Cochrane Central Register of Controlled Trials (CENTRA …
These speech difficulties could be due to structural, sensory or neurophysiological causes (e.g. hearing impairment), but more often …
Consensus practice parameter: audiological assessment and management of unilateral hearing loss in children.
Bagatto M, DesGeorges J, King A, Kitterick P, Laurnagaray D, Lewis D, Roush P, Sladen DP, Tharpe AM. Bagatto M, et al. Int J Audiol. 2019 Dec;58(12):805-815. doi: 10.1080/14992027.2019.1654620. Epub 2019 Sep 5. Int J Audiol. 2019. PMID: 31486692 Review.
Objective: Provide recommendations to audiologists for the management of children with unilateral hearing loss (UHL) and for needed research that can lend further insight into important unanswered questions.Design: An international panel of experts on children with UHL was …
Objective: Provide recommendations to audiologists for the management of children with unilateral hearing loss (UHL) and for needed r …
Inner ear disorders.
Smouha E. Smouha E. NeuroRehabilitation. 2013;32(3):455-62. doi: 10.3233/NRE-130868. NeuroRehabilitation. 2013. PMID: 23648600 Review.
OBJECTIVES: To present a framework for the diagnosis and treatment of inner ear disorders, with an emphasis on problems common to neuro-rehabilitation. INTRODUCTION: Disorders of the inner ear can cause hearing loss, tinnitus, vertigo and imbalance. Hearing loss can …
OBJECTIVES: To present a framework for the diagnosis and treatment of inner ear disorders, with an emphasis on problems common to neuro-reha …
Autism intervention meta-analysis of early childhood studies (Project AIM): updated systematic review and secondary analysis.
Sandbank M, Bottema-Beutel K, Crowley LaPoint S, Feldman JI, Barrett DJ, Caldwell N, Dunham K, Crank J, Albarran S, Woynaroski T. Sandbank M, et al. BMJ. 2023 Nov 14;383:e076733. doi: 10.1136/bmj-2023-076733. BMJ. 2023. PMID: 37963634 Free PMC article.
DATA SOURCES: A search was conducted in November 2021 (updating a search done in November 2017) of the following databases and registers: Academic Search Complete, CINAHL Plus with full text, Education Source, Educational Administration Abstracts, ERIC, Medline, ProQuest D …
DATA SOURCES: A search was conducted in November 2021 (updating a search done in November 2017) of the following databases and registers: Ac …
Replication in Evidence-Based Aphasia Treatments.
Karidas S, Hinckley JJ, Brekher I. Karidas S, et al. J Speech Lang Hear Res. 2023 Jun 20;66(6):1958-1966. doi: 10.1044/2022_JSLHR-21-00688. Epub 2023 Jan 3. J Speech Lang Hear Res. 2023. PMID: 36596266 Review.
PURPOSE: A critical review was completed to evaluate replication of aphasia treatments that have been vetted and accepted on the American Speech-Language-Hearing Association Practice Portal. METHOD: The electronic databases Academic Search Premier, ProQuest Central, CINAHL …
PURPOSE: A critical review was completed to evaluate replication of aphasia treatments that have been vetted and accepted on the American Sp …
Immersive technology and the elderly: a mini-review.
Shelton BE, Uz C. Shelton BE, et al. Gerontology. 2015;61(2):175-85. doi: 10.1159/000365754. Epub 2014 Dec 10. Gerontology. 2015. PMID: 25502624 Free article. Review.
A narrative literature review was conducted using the ScienceDirect, EBSCOhost, Springerlink and ERIC databases to summarize primary studies from which conclusions were drawn into a holistic interpretation. The majority of the studies examined the effect of immersive techn …
A narrative literature review was conducted using the ScienceDirect, EBSCOhost, Springerlink and ERIC databases to summarize primary …
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History.
Nisenbaum E, Yan D, Shearer AE, de Joya E, Thielhelm T, Russell N, Staecker H, Chen Z, Holt JR, Liu X. Nisenbaum E, et al. Audiol Neurootol. 2023;28(6):407-419. doi: 10.1159/000528766. Epub 2023 Jun 16. Audiol Neurootol. 2023. PMID: 37331337 Free PMC article. Review.
BACKGROUND: Mutations in TMPRSS3 are an important cause of autosomal recessive non-syndromic hearing loss. The hearing loss associated with mutations in TMPRSS3 is characterized by phenotypic heterogeneity, ranging from mild to profound hearing loss, and is g …
BACKGROUND: Mutations in TMPRSS3 are an important cause of autosomal recessive non-syndromic hearing loss. The hearing loss as …
Coalition for Global Hearing Health Hearing Care Pathways Working Group: Guidelines for Clinical Guidance for Readiness and Development of Evidence-Based Early Hearing Detection and Intervention Programs.
Yoshinaga-Itano C, Carr G, Davis A, Ching TYC, Chung K, Clark J, Harkus S, Kuan ML, Garg S, Adreoli Balen S, O'Leary S. Yoshinaga-Itano C, et al. Ear Hear. 2024 May 24. doi: 10.1097/AUD.0000000000001501. Online ahead of print. Ear Hear. 2024. PMID: 38783422
The goal of universal newborn hearing screening is to enable the detection of hearing loss in infants so that timely health and educational/therapeutic intervention can be provided as early as possible to improve outcomes. While many countries have implemented unive …
The goal of universal newborn hearing screening is to enable the detection of hearing loss in infants so that timely health an …
97 results