Hearing problems in patients with hereditary gelsolin amyloidosis

Tuuli Mustonen; Ville Sivonen; Sari Atula; Sari Kiuru-Enari; Saku T. Sinkkonen

doi:10.1186/s13023-021-02077-9

Hearing problems in patients with hereditary gelsolin amyloidosis

Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari, Saku T. Sinkkonen

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Article number	448
Journal	Orphanet journal of rare diseases
Volume	16
Issue number	1
Number of pages	8
ISSN	1750-1172
DOIs	https://doi.org/10.1186/s13023-021-02077-9
Publication status	Published - 24 Oct 2021
MoE publication type	A1 Journal article-refereed

Bibliographical note

Publisher Copyright:
© 2021, The Author(s).

Fields of Science

3125 Otorhinolaryngology, ophthalmology
Automated audiometry
Gelsolin amyloidosis
Hearing loss
Speech Spatial and Qualities of Hearing Scale
Speech-in-noise
MATRIX SENTENCE TEST
FAMILIAL AMYLOIDOSIS
INVOLVEMENT
MUTATION
EAR
FINNISH TYPE
SPEECH

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10.1186/s13023-021-02077-9

Hearing problems in patients with hereditary gelsolin amyloidosisFinal published version, 2.36 MBLicence: CC BY

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title = "Hearing problems in patients with hereditary gelsolin amyloidosis",

keywords = "3125 Otorhinolaryngology, ophthalmology, Automated audiometry, Gelsolin amyloidosis, Hearing loss, Speech Spatial and Qualities of Hearing Scale, Speech-in-noise, MATRIX SENTENCE TEST, FAMILIAL AMYLOIDOSIS, INVOLVEMENT, MUTATION, EAR, FINNISH TYPE, SPEECH",

author = "Tuuli Mustonen and Ville Sivonen and Sari Atula and Sari Kiuru-Enari and Sinkkonen, {Saku T.}",

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AU - Mustonen, Tuuli

AU - Sivonen, Ville

AU - Atula, Sari

AU - Kiuru-Enari, Sari

AU - Sinkkonen, Saku T.

PY - 2021/10/24

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KW - 3125 Otorhinolaryngology, ophthalmology

KW - Automated audiometry

KW - Gelsolin amyloidosis

KW - Hearing loss

KW - Speech Spatial and Qualities of Hearing Scale

KW - Speech-in-noise

KW - MATRIX SENTENCE TEST

KW - FAMILIAL AMYLOIDOSIS

KW - INVOLVEMENT

KW - MUTATION

KW - EAR

KW - FINNISH TYPE

KW - SPEECH

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U2 - 10.1186/s13023-021-02077-9

DO - 10.1186/s13023-021-02077-9

M3 - Article

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VL - 16

JO - Orphanet journal of rare diseases

JF - Orphanet journal of rare diseases

IS - 1

M1 - 448

ER -

Hearing problems in patients with hereditary gelsolin amyloidosis

Bibliographical note

Fields of Science

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