Citations (31)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (5)
Pinar Altiaylik Ozer, Emrah Utku Kabatas, Gokce Tasdemir Ertugrul, Bengi Ece Kurtul, Umut Kaygusuz & Selmin Karatayli Ozgursoy. (2018) Ocular Disorders in Turkish Children with Sensorineural Hearıng Loss: A Cross-Sectional Study and Literature Review. Seminars in Ophthalmology 33:2, pages 155-160.
Read now
Read now
Jie Chen, Qinjun Wei, Jun Yao, Xiaoyun Qian, Yanhong Dai, Ye Yang, Xin Cao & Xia Gao. (2013) Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings. International Journal of Audiology 52:2, pages 134-138.
Read now
Read now
Joaquin Lado Abeal. (2008) Pendred syndrome. Expert Review of Endocrinology & Metabolism 3:5, pages 635-643.
Read now
Read now
Sasan Sharghi, Vahid Haghpanah, Ramin Heshmat, Armaghan Fard-Esfahani, Homayoun Hadizadeh, Anahita Lashkari, Ozra Tabatabaei, Eghbal Taheri, Massoud Motesaddi, Alireza Mojtahedi & Bagher Larijani. (2007) Comparison of MRI findings with traditional criteria in diagnosis of Pendred syndrome. International Journal of Audiology 46:2, pages 69-74.
Read now
Read now
Tamie Mimura, Eisuke Sato, Makoto Sugiura, Takahiko Yoshino, Shinji Naganawa & Tsutomu Nakashima. (2005) Hearing loss in patients with enlarged vestibular aqueduct: Air-bone gap and audiological Bing test. International Journal of Audiology 44:8, pages 466-469.
Read now
Read now
Articles from other publishers (26)
Julia Dlugaiczyk. (2021) Seltene Erkrankungen des vestibulären Labyrinths: von Zebras,
Chamäleons und Wölfen im Schafspelz. Laryngo-Rhino-Otologie 100:S 01, pages S1-S40.
Crossref
Crossref
Elizabeth M. Ketchum, Sydney N. Sheltz-Kempf & Jeremy S. Duncan. 2020. The Senses: A Comprehensive Reference. The Senses: A Comprehensive Reference
129
144
.
Catherine Peters & Nadia Schoenmakers. 2019. Brook's Clinical Pediatric Endocrinology. Brook's Clinical Pediatric Endocrinology
289
334
.
Kornelia Woźniczko, Joanna Rajchel, Beata Dziendziel & Piotr Skarżyński. (2020) Characteristic of hearing loss in children with
Pendred syndrome and results of its treatment
with cochlear implants – a literature review. Nowa Audiofonologia 8:2, pages 20-25.
Crossref
Crossref
Nadia Schoenmakers. 2019. Encyclopedia of Endocrine Diseases. Encyclopedia of Endocrine Diseases
296
312
.
О. Л. Миронович, Е.А. Близнец, Т.Г. Маркова, Е. Н. Гептнер, М. Р. Лалаянц, Е. И. Зеликович, Г. А. Таварткиладзе & А.В. Поляков. (2017) РЕЗУЛЬТАТЫ МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКОГО ИССЛЕДОВАНИЯ РОССИЙСКИХ ПАЦИЕНТОВ С СИНДРОМОМ ПЕНДРЕДА И АЛЛЕЛЬНЫМИ ЗАБОЛЕВАНИЯМИ, "Генетика". Генетика:1, pages 88-99.
Crossref
Crossref
O. L. Mironovich, E. A. Bliznetz, T. G. Markova, E. N. Geptner, M. R. Lalayants, E. I. Zelikovich, G. A. Tavartkiladze & A. V. Polyakov. (2017) Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders. Russian Journal of Genetics 53:1, pages 128-138.
Crossref
Crossref
Amiel A. Dror & Karen B. Avraham. 2017. The Role of Pendrin in Health and Disease. The Role of Pendrin in Health and Disease
23
36
.
T. G. Markova, E. N. Geptner, M. R. Lalayants, E. I. Zelikovich, T. I. Chugunova, O. L. Mironovich, E. A. Bliznetz, A. V. Polyakov & G. A. Tavartkiladze. (2016) The clinical definition and etiology of Pendred syndrome (a review of the literature and clinical observations). Vestnik otorinolaringologii 81:6, pages 25.
Crossref
Crossref
Andreas Moraitis & Constantine A. Stratakis. 2016. Thyroid Cancer. Thyroid Cancer
43
70
.
Kay W. Chang. (2015) Genetics of Hearing Loss—Nonsyndromic. Otolaryngologic Clinics of North America 48:6, pages 1063-1072.
Crossref
Crossref
Michael Parker & Maria Bitner-Glindzicz. (2015) Republished: Genetic investigations in childhood deafness. Postgraduate Medical Journal 91:1077, pages 395-402.
Crossref
Crossref
Michael Parker & Maria Bitner-Glindzicz. (2015) Genetic investigations in childhood deafness. Archives of Disease in Childhood 100:3, pages 271-278.
Crossref
Crossref
Yunxia Wang Lundberg, Yinfang Xu, Kevin D. Thiessen & Kenneth L. Kramer. (2015) Mechanisms of otoconia and otolith development. Developmental Dynamics 244:3, pages 239-253.
Crossref
Crossref
Miriam LadsousVirginie Vlaeminck-GuillemViviane DumurChristophe VincentFrédérique DubrulleClaire-Marie DhaenensJean-Louis Wémeau. (2014) Analysis of the Thyroid Phenotype in 42 Patients with Pendred Syndrome and Nonsyndromic Enlargement of the Vestibular Aqueduct. Thyroid 24:4, pages 639-648.
Crossref
Crossref
Hyoung-Mi Kim & Philine Wangemann. (2011) Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin. PLoS ONE 6:3, pages e17949.
Crossref
Crossref
S. Wiener-Vacher. (2010) Vertiges chez l'enfant. EMC - Pédiatrie - Maladies infectieuses 5:1, pages 1-9.
Crossref
Crossref
S. Wiener-Vacher. (2010) Vértigo infantil. EMC - Pediatría 45:2, pages 1-9.
Crossref
Crossref
Álvaro García-Manzanares Vázquez, Irene Gonzalo Montesinos, Águeda Muñoz Jiménez, Jose Antonio rubio García, Javier Galipenzo García & Julia Álvarez Hernández. (2009) Síndrome de Pendred: una causa de bocio relacionada con sordera. Endocrinología y Nutrición 56:8, pages 428-430.
Crossref
Crossref
Philine Wangemann. 2008. Auditory Trauma, Protection, and Repair. Auditory Trauma, Protection, and Repair
49
100
.
Ralph S. Lachman. 2007. Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias. Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias
612
680
.
Philine Wangemann. (2006) Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential. The Journal of Physiology 576:1, pages 11-21.
Crossref
Crossref
Nicole Pfarr, Guntram Borck, Andrew Turk, Ulrike Napiontek, Annerose Keilmann, Wibke Müller-Forell, Peter Kopp & Joachim Pohlenz. (2006) Goitrous Congenital Hypothyroidism and Hearing Impairment Associated with Mutations in the TPO and SLC26A4/PDS Genes. The Journal of Clinical Endocrinology & Metabolism 91:7, pages 2678-2681.
Crossref
Crossref
N Loundon, I Rouillon, N Munier, S Marlin, G Roger & E N Garabedian. (2005) Cochlear Implantation in Children with Internal Ear Malformations. Otology & Neurotology 26:4, pages 668-673.
Crossref
Crossref
Moshe Goldfeld, Benjamin Glaser, Elias Nassir, John Moshe Gomori, Elitsur Hazani & Nassir Bishara. (2005) CT of the Ear in Pendred Syndrome. Radiology 235:2, pages 537-540.
Crossref
Crossref
Ulrike Napiontek, Guntram Borck, Wiebke Müller-Forell, Nicole Pfarr, Andrea Bohnert, Annerose Keilmann & Joachim Pohlenz. (2004) Intrafamilial Variability of the Deafness and Goiter Phenotype in Pendred Syndrome Caused by a T416P Mutation in the SLC26A4 Gene. The Journal of Clinical Endocrinology & Metabolism 89:11, pages 5347-5351.
Crossref
Crossref