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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 2
1993 1
1999 1
2001 2
2004 2
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2009 1
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2012 1
2015 1
2018 1
2021 2
2024 0

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Quoted phrase not found in phrase index: "Mild neurosensory hearing impairment"
Page 1
Dominant optic atrophy.
Lenaers G, Hamel C, Delettre C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P, Milea D. Lenaers G, et al. Orphanet J Rare Dis. 2012 Jul 9;7:46. doi: 10.1186/1750-1172-7-46. Orphanet J Rare Dis. 2012. PMID: 22776096 Free PMC article. Review.
About 20% of DOA patients harbour extraocular multi-systemic features, including neurosensory hearing loss, or less commonly chronic progressive external ophthalmoplegia, myopathy, peripheral neuropathy, multiple sclerosis-like illness, spastic paraplegia or …
About 20% of DOA patients harbour extraocular multi-systemic features, including neurosensory hearing loss, or less com …
Diagnostic and severity scores for Cockayne syndrome.
Spitz MA, Severac F, Obringer C, Baer S, Le May N, Calmels N, Laugel V. Spitz MA, et al. Orphanet J Rare Dis. 2021 Feb 3;16(1):63. doi: 10.1186/s13023-021-01686-8. Orphanet J Rare Dis. 2021. PMID: 33536051 Free PMC article.
A severity score for CS was designed on five items (head circumference, growth failure, neurosensorial signs, motor autonomy, communication skills) and validated by comparison with classical predefined severity subtypes of CS. RESULTS: Short stature, enophtalmos, hearin …
A severity score for CS was designed on five items (head circumference, growth failure, neurosensorial signs, motor autonomy, communi …
Etiologies of hearing impairment among infants and toddlers: 1986-1987 versus 2001.
Gruss I, Berlin M, Greenstein T, Yagil Y, Beiser M. Gruss I, et al. Int J Pediatr Otorhinolaryngol. 2007 Oct;71(10):1585-9. doi: 10.1016/j.ijporl.2007.06.019. Epub 2007 Aug 15. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17706796
No changes in gender and age at time of admission were found. The prevalence of mild-to-moderate hearing loss was higher in Group II while severe and profound hearing loss was more prevalent in Group I. ...Since no significant association betwee …
No changes in gender and age at time of admission were found. The prevalence of mild-to-moderate hearing loss was highe …
Universal newborn hearing screening in the Italian Region of Sicily in 2018.
Ferlito S, Maniaci A, Cocuzza S, La Mantia I, Di Mauro P, Poli G, Maiolino L, Coco S, Merlino F, Maltese M, Ragliani M, Russo M, Gulino A, Azieli C, Martines F, Galletti F, Bubbico L. Ferlito S, et al. Acta Otorhinolaryngol Ital. 2021 Aug;41(4):356-363. doi: 10.14639/0392-100X-N1162. Acta Otorhinolaryngol Ital. 2021. PMID: 34533539 Free PMC article.
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss, number of infants "referred" to transiently evoked otoacoustic emissions (TEOAE), number of infants with pathologic auditory brainstem res …
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss …
Predictive Factors for Vestibular Loss in Children With Hearing Loss.
Janky KL, Thomas MLA, High RR, Schmid KK, Ogun OA. Janky KL, et al. Am J Audiol. 2018 Mar 8;27(1):137-146. doi: 10.1044/2017_AJA-17-0058. Am J Audiol. 2018. PMID: 29482202 Free PMC article.
PURPOSE: The aim of this study was to determine if there are factors that can predict whether a child with hearing loss will also have vestibular loss. METHOD: A retrospective chart review was completed on 186 children with hearing loss s …
PURPOSE: The aim of this study was to determine if there are factors that can predict whether a child with hearing loss …
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism.
Bruno R, Aversa T, Catena M, Valenzise M, Lombardo F, De Luca F, Wasniewska M. Bruno R, et al. Hear Res. 2015 Sep;327:43-7. doi: 10.1016/j.heares.2015.04.018. Epub 2015 May 15. Hear Res. 2015. PMID: 25987501
All the selected patients underwent, at a median age of 15.4 years, an audiologic investigation, which evidenced a mild and subclinical hearing loss in 25% of them. The poorest hearing scores were recorded in the individuals with athyreosis and in thos …
All the selected patients underwent, at a median age of 15.4 years, an audiologic investigation, which evidenced a mild and subclinic …
Auditory abnormalities associated with unilateral renal agenesis.
Huang HM, Yeh RM, Tan CT, Chao MM, Lin KN. Huang HM, et al. Int J Pediatr Otorhinolaryngol. 2001 Aug 20;60(2):113-8. doi: 10.1016/s0165-5876(01)00501-8. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11518587
Two were diagnosed with mild sensorineural hearing impairment while the other two had moderate hearing loss. CONCLUSIONS: The results of our study suggest that neurosensory hearing loss was found to be associated with renal …
Two were diagnosed with mild sensorineural hearing impairment while the other two had moderate hearing loss …
Outcome at 14 years of extremely low birthweight infants: a regional study.
Doyle LW, Casalaz D; Victorian Infant Collaborative Study Group. Doyle LW, et al. Arch Dis Child Fetal Neonatal Ed. 2001 Nov;85(3):F159-64. doi: 10.1136/fn.85.3.f159. Arch Dis Child Fetal Neonatal Ed. 2001. PMID: 11668155 Free PMC article.
OBJECTIVES: To determine the neurosensory outcome at 14 years of age of a regional cohort of extremely low birthweight (ELBW) children, to contrast their prognosis with normal birthweight (NBW) controls, and to determine the predictive value of assessments ea …
OBJECTIVES: To determine the neurosensory outcome at 14 years of age of a regional cohort of extremely low birthweight (ELBW) childre …
Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
Ben Rebeh I, Morinière M, Ayadi L, Benzina Z, Charfedine I, Feki J, Ayadi H, Ghorbel A, Baklouti F, Masmoudi S. Ben Rebeh I, et al. Mol Vis. 2010 Sep 30;16:1898-906. Mol Vis. 2010. PMID: 21031134 Free PMC article.
PURPOSE: Recessive mutations of the myosin VIIA (MYO7A) gene are reported to be responsible for both a deaf-blindness syndrome (Usher type 1B [USH1B] and atypical Usher syndrome) and nonsyndromic hearing loss (HL; Deafness, Neurosensory, Autosomal Recessive 2 …
PURPOSE: Recessive mutations of the myosin VIIA (MYO7A) gene are reported to be responsible for both a deaf-blindness syndrome (Usher type 1 …
Extremely low birthweight infants at 3 years: a developmental profile.
Bowen JR, Starte DR, Arnold JD, Simmons JL, Ma PJ, Leslie GI. Bowen JR, et al. J Paediatr Child Health. 1993 Aug;29(4):276-81. doi: 10.1111/j.1440-1754.1993.tb00511.x. J Paediatr Child Health. 1993. PMID: 7690580

At 3 years, 6 (12%) children had severe neurodevelopmental impairment (severe cerebral palsy, blindness, deafness or a General Quotient (GQ) < 70 on the Griffiths Scales), 11 (21%) had mild to moderate impairment and 35 (67%) had no neurosensory

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At 3 years, 6 (12%) children had severe neurodevelopmental impairment (severe cerebral palsy, blindness, deafness or a General Quotie …
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