Results 191 to 200 of about 325,838 (344)

Discrimination of formant transition tempo by hearing-impaired listeners [PDF]

, 1977
Sally G. Revoile, Mary Pat Wilson, J. M. Pickett   +2 more
openalex   +1 more source

Syndrome of the Month: Bosma Arhinia Microphthalmia Syndrome

American Journal of Medical Genetics Part A, EarlyView.
Katherine J. K. Patterson, John M. Graham Jr, Natalie D. Shaw   +2 more
wiley   +1 more source

Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome (OMIM #619080)

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, Alessia Nisco, Luciana de Gennaro, Maria Tolomeo, Elisa Lorefice, Giuseppe Petrosillo, Silvia Russo, Donatella De Giovanni, Claudia Rita Catacchio, Francesca Romana Lepri, Mario Ventura, Simonetta Simonetti, Albina Tummolo, Maria Barile   +13 more
wiley   +1 more source

Emotional and behavioral problems in children and adolescents with hearing impairment. [PDF]

BMC Pediatr
Fahim DFM, Sayed SI, Abdelrazic MI, Abuelela IS.   +3 more
europepmc   +1 more source

Speech and Hearing of the Hearing Impaired Students in the Junior High School

, 1971
Noriko Kawai, Seiji Inoue, Keiichi Date, Tomohiro Yasuno   +3 more
openalex   +2 more sources

Some characteristics of oral air flow for fricative consonants produced by hearing-impaired speakers [PDF]

, 1978
Robert L. Whitehead, Sidney M. Barefoot, Ann K. Lieberth   +2 more
openalex   +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, Ruth Braden, David J. Amor, Angela T. Morgan   +3 more
wiley   +1 more source

Deep learning-based classification of speech disorder in stroke and hearing impairment. [PDF]

PLoS One
Park JK, Mun SB, Kim YJ, Kim KG.
europepmc   +1 more source

The Efficieney of Hearing Aid Use of Hearing Impaired Children in Special Class

, 1972
Hideo Iwaguchi, Toshihiko Yokoyama
openalex   +2 more sources

A test to determine the auditory speech perception ability of hearing-impaired children [PDF]

, 1978
K. O. Jones, Robert L. Whitehead
openalex   +1 more source