Low-frequency interaural time differences and available localization cues in the azimuthal plane for listeners with head-worn or body-worn hearing aid(s) [PDF]
, 1979 George F. Kuhn, Tom Munro
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American Journal of Community Psychology, EarlyView.Abstract We explored community‐based doulas' perspectives on the acceptability of using formal screening tools to address low rates of mental health screening, diagnosis, and treatment for perinatal anxiety and depression among Black women. Using thematic analysis, we analyzed interview data from 30 community‐based doulas who support Black families ...
Tamara Nelson +5 more
wiley +1 more source
Speechreading Test Using a Video Tape Recorder and Its Application to Hearing Aid Evaluation
, 1975 Yoshisato Tanaka, Fumiko Chiba
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Acoustical Factors Affecting Hearing Aid Performance , edited by G. A. Studebaker and I. Hochberg [PDF]
, 1982 Lois L. Elliott
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT This study presents the case of a child with multiple congenital anomalies, severe hypotonia, and profound bilateral sensorineural hearing loss. Functional bioenergetic assessments showed no significant mitochondrial respiratory defects, and riboflavin (Rf) status evaluation excluded a deficiency in Rf transporters as a cause of hearing loss ...
Piero Leone +13 more
wiley +1 more source
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison +3 more
wiley +1 more source
Effect of number of channels on the performance of a multichannel compression hearing aid [PDF]
, 1989 E. William Yund, Krista M. Buckles
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Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim +2 more
wiley +1 more source
Comparison of four hearing aid prescriptive procedures [PDF]
, 1986 Jean Sullivan +3 more
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Down Syndrome in Maternity Care: Mothers' Experiences of Prenatal Screening
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Prenatal screening for Down syndrome (DS) is offered to expectant parents receiving antenatal care in many countries, with an emphasis on providing parents with the opportunity to make informed choices about their pregnancy. We examined experiences of prenatal screening among mothers of children with DS living in England, Scotland, or Wales ...
Tamar Rutter +5 more
wiley +1 more source